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rVue Holdings, Inc., Reports Complete Year 2012 Financial Results

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Chicago, IL (PRWEB) July 05, 2013

rVue Holdings, Inc. (OTCBB: RVUE) the premier marketing technologies platform for digital out of property media announced its financial results for the complete year ended December 31, 2012.

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Summary Results for the Full Year of 2012:

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-Total income was $ 602,363 for fiscal 2012 down slightly from $ 643,483 in the prior year.&#13

-Core Costs: This is the concentrate of our organization and source of future development. Core revenue for the years ended December 31, 2012 and 2011 had been, $ 197,444 and $ 203,276, respectively.&#13

-Non-Core Costs: For the years ended December 31, 2012 and 2011 have been $ 404,919 and $ 440,207, respectively. The decline was due to the end of a management relationship with Auto Nation. This trend will continue in 2013 as we focus much more resources on core enterprise efforts. In addition the Mattress Firm merged with Mattress Giant and we respectfully agree not to renew for 2013. (this represented approximately $ 230,000 in revenue ) .&#13

-Promoting, general and administrative expenses was $ two,328,669 in the complete year of 2012, compared to $ three,339,359 for the complete year of 2011, a reduction of $ 1,010,690 in the year due to price controls, alter in management and a shift to much more media focused transactions.&#13

-Net loss for the complete year of 2012 was ($ three,839,348) compared to a net loss of ($ three,616,973) in the 2011.&#13

-As of December 31, 2012 the organization had $ 850,000 of cash.

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As Michael Mullarkey (prior CEO and Executive Chairman) described, 2012 was a transformative year for the firm. We established our leadership position as the largest outside digital media platform connecting more than 770,000 screens across 180+ networks.”

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Mark Pacchini (CEO and President) added, “With our expenses under much better handle, our focus going forward will be on providing our consumers with business building ideas and globe class service. If we deliver this, it must outcome in revenue development.”

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Conference Contact Details:

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A conference get in touch with will take location at 9:00 a.m. CST, on &#13

Tuesday, July 9, 2013. &#13

Anyone interested in participating must get in touch with *Toll-Cost-free: &#13

(866) 376-0342 &#13

International dial-in number: (408) 773-6761&#13

Conference code: 3986559170

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About rVue:&#13

rVue Holdings, Inc. is an advertising technologies business offering the digital distribution platform for the Digital Outdoor Marketing business. The firm connects 770,000 digital screens across 180 networks delivering access to 250 million every day impressions in a single simple platform. Backed by the industry’s most intuitive and intelligent platform, rVue has the technologies, data and experience to connect brands and targeted consumers where and when it matters most. For much more details, please check out http://www.rvue.com.

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Make contact with Details:

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Business and Press Inquiries: &#13

rVue Holdings, Inc. &#13

Dean Peterson &#13

dean.peterson(at)rvue(dot)com &#13

312.219.8835

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Forward Hunting Statements: &#13

This press release consists of “forward hunting statements” within the which means of the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. The statements contained in this press release that are not purely historical are forward-searching statements. Forward-hunting statements give the Company’s present expectations or forecasts of future events. Such statements are topic to risks and uncertainties that are frequently tough to predict and beyond the Company’s handle, and could cause the Company’s results to differ materially from those described. The Business is offering this information as of the date of this press release and does not undertake any obligation to update any forward hunting statements contained in this press release as a outcome of new information, future events or otherwise. We have primarily based these forward-seeking statements largely on our present expectations and projections about future events and economic trends affecting the financial situation of our enterprise. Forward seeking statements need to not be read as a assure of future functionality or outcomes, and will not necessarily be accurate indications of the times at, or by, which such overall performance or outcomes will be achieved. Important aspects that could lead to such differences consist of, but are not limited to, the Threat Aspects and other data set forth in the Company’s Annual Report on Form 10-K to be filed these days and in our other filings with the Securities and Exchange Commission.

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Medtronic Infuse Bone Graft Failure Allegation Lawsuits Update: Resource4thePeople Reports New Analysis Findings Raise Issues about Side Effects

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San Diego, CA (PRWEB) July 05, 2013

http://www.resource4thepeople.com/defectivemedicaldevices/medtronic.html

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Resource4thePeople, in its latest update to customers impacted by operations involving healthcare devices, these days announced that the findings of a two-year study by Yale University researchers have raised issues about the marketing and advertising and security of Medtronic Infuse bone grafts similar to those integrated in allegations now being reviewed.

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The Yale University study, which was published* June 18, 2013 in the Annals of Internal Medicine, was undertaken as an independent study following the health-related devices were the topic of a Class 1 Recall by the Meals and Drug Administration** and a highly vital report*** from a U.S. Senate committee that raised concerns about conflicts of interest simply because of payments the organization produced to health-related researchers and physicians.

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Studies funded by Medtronic underplayed the advantages of the Infuse bone grafts and failed to report numerous critical side effects, according to both Yale researchers and Senate investigators. The Yale researchers reported such severe side effects as excessive bone development, male sterility, inflammations and paralysis, according to the report.

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The findings of this study are constant with some of the allegations that we have been getting in rising numbers considering that the release of the Senates report, said Resource4thePeople.

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We anticipate that the news of the Yale researchers findings will generate even a lot more inquiries from customers about the legal possibilities they might have to seek compensation and consequently, we will continue to provide totally free legal consultations and overview these claims.

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The Yale researchers had been crucial of prior Medtronic-funded study research which provided endorsements of the safety and effectiveness of the Infuse bone grafts. The Yale researchers help those research had been biased, as did Senate investigators in their report.

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The Yale researchers summarized their findings in comparing the Medtronic Infuse bone graft (rhBMP-2) to conventional therapy by saying:

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In conclusion, we discovered substantial proof of reporting bias and no proof that rhBMP-2 is a lot more effective than ICBG in spinal fusion, with some evidence of an association with crucial harms. Far more study is needed to offer a lot more trustworthy estimates of danger for cancer and other adverse events and to determine patient populations in which use of rhBMP-two could be beneficial, such as circumstances where use of bone graft alone is related with a high danger for pseudarthrosis. On the basis of the currently offered evidence, it is difficult to recognize clear indications for rhBMP-two in spinal fusion.

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Resource4thePeople stated it will also continue to offer normal updates supplying buyers who might have been impacted by remedy with Medtronic Infuse bone grafts with data about research and legal developments involving the devices.

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This will continue to be an region of prime concentrate for us as we provide buyers legal options involving allegations that the Medtronic Infuse Bone Grafts might have caused critical, life-threatening health issues, mentioned Resource4thePeople.

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Amongst the allegations we are investigating are claims from buyers alleging that the Medtronic Infuse Bone Grafts had been utilised improperly in medical operations and caused serious side effects to sufferers.

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Resource4thePeople also mentioned that its national network of attorneys will continue to review claims from customers who are alleging they could have suffered extreme back and leg discomfort, infections, bone deterioration, sterility and cancer, amongst other troubles.

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In the FDAs Feb. 16, 2011 Class 1 Recall** of Medtronic Infuse Bone Graft pumps and refill kits, the FDA warned that the merchandise “may outcome in patient harm, serious injury, and/or death due to drug overdose or underdose.

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Class I recalls are the most severe variety of recall and involve situations in which there is a reasonable probability that use of these merchandise will lead to significant adverse overall health consequences or death.

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Resource4thePeoples legal group is also investigating claims similar to those contained in a federal lawsuit**** filed in March in the Southern District of Ohio against Medtronic Inc. and an Ohio surgeon who, according to complaint, was a paid Medtronic consultant in addition to his professional duties.

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The lawsuit includes allegations that 88 sufferers are claiming that underwent spine surgeries involving bone protein that they did not consent to and have suffered detrimental side effects for which they are searching for compensation.

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The lawsuit claims that “medically unnecessary, experimental spine surgeries” had been performed “using falsely and improperly marketed Medtronic healthcare devices and drugs,” according to allegations contained in the court file.

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Resource4thePeople also stated that the allegations filed in the lawsuit raise far more inquiries about the relationships between physicians and Medtronic over costs paid to the medical doctors that have come beneath criticism from the U.S. Senate Finance Committee investigators.

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The revelations integrated in the Oct. 25, 2012 report by the Senate Finance Committee involving payments to doctors and the downplaying of dangerous side effects from this healthcare device have raised significant questions amongst patients who underwent these surgeries and have contacted us,” mentioned Resource4thePeople.

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Resource4thePeople said that over the final few months such inquiries have enhanced as a outcome of news media reports about the findings of the committees investigation into Medtronics spending of millions of dollars to physicians and researchers in return for studies favorable to the Infuse device.

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The Medtronic Infuse bone graft was approved by the Food and Drug Administration as a sanctioned medical device made to stimulate spinal bone development in individuals suffering from reduce spine degenerative diseases.

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Sources:&#13

*http://annals.org/post.aspx?articleid=1696646&#13

**http://www.fda.gov/MedicalDevices/Safety/ListofRecalls/ucm243634.htm&#13

***http://www.finance.senate.gov/newsroom/chairman/release/?id=b1d112cb-230f-4c2e-ae55-13550074fe86&#13

****Case # 1:13cv0202 U.S. District Court, Southern District of Ohio

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Foods4BetterHealth Reports on Splenda Controversy: Study

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Boston, MA (PRWEB) June 28, 2013

Foods4BetterHealth.com, a new food and nutrition net web site that believes in employing food to heal and prevent illness and illness and help you live a extended, pleased life, has released a report on the newest controversy concerning the artificial sweetener sucralose, frequently identified by the brand name Splenda.

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As Foods4BetterHealth reports (http://www.foods4betterhealth.com/the-latest-controversy-dr-kevins-take-on-the-splenda-debate-2555), the Center for Science in the Public Interest, a consumer advocate group, recently announced that they were downgrading sucralose from “protected” to “caution” status after an unpublished study carried out in Italy by scientist Dr. Morando Soffritti located that sucralose brought on cancer in mice. (Supply: Center for Science in the Public Interest, CSPI downgrades Splenda from safe to caution, http://www.cspinet.org/new/201306121.html, June 12, 2013.) As a outcome of his research, Soffritti advised that ladies and kids should not eat sucralose and that more research is required. (Supply: Butterworth, T., Controversial Italian Scientist Says Splenda Causes Cancer, Forbes web site http://www.forbes.com/web sites/trevorbutterworth/2012/04/24/controversial-italian-scientist-says-splenda-causes-cancer/#, last accessed June 18, 2013.)

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As the article The Latest Controversy: Dr. Kevins Take on the Splenda Debate notes, up till lately, Splenda has been identified as a secure sweetener, with no adverse effects or unfavorable aftertaste, in contrast to many other sweeteners on the market place. Dr. Kevin notes that Splenda has been endorsed by the American Diabetes Association, the Globe Overall health Organization, the Food and Drug Administration, and several far more as a safe alternative to sugar that can be useful in curbing rates of obesity and kind 2 diabetes.

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The Foods4BetterHealth report states that this unpublished study has received significant media attention in the previous few weeks, however no a single has deemed the fact that the scientist who carried out the study, as well as the institute where he performs, has been in hot water ahead of for a lack of top quality manage and improper experimental designs in prior studies. (Supply: Update on Ramazzini Institute Data in IRIS Assessments, U.S. Environmental Protection Agency, http://www.epa.gov/iris/ramazzini.htm, last accessed June 18, 2013.)

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The report concludes that, according to Dr. Kevin, there is no want to cease consuming Splenda just yet. Based on his investigation, Dr. Kevin was capable to conclude that Splenda is a safe sweetener that can be utilized in baking and/or cooking.

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Foods4BetterHealth.com, designed by Doctors Overall health Press, is a food news and health net web site, providing readers info about the newest meals controversies, exclusive professional tips, and overall health guidelines to ward off illness, avert illness, and reside a extended, healthier life. For a lot more data, go to http://www.foods4betterhealth.com.

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Leadsnet Inc. Reports Enhanced Loan Modifications

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South Lake Tahoe, CA (PRWEB) February 6, 2009

Leadsnet Inc., has reported that lenders are stepping up their efforts to modify loans by providing principle reductions, interest rate reductions and forgiveness of back payments. Government and enterprise leaders are calling for improved loan modifications and banks are responding. Wells Fargo, Bank of America, Citigroup and government agencies such as the FDIC, Federal Reserve, Fannie Mae and Freddie Mac have all introduced a myriad of applications in response to the economic reality that over five million homes will be at some stage of the foreclosure procedure this year.

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“Recent moves by lenders across the board has lead to elevated modifications with favorable terms” says Ted Schmidt. President of Leadsnet Inc., http://www.loanmodificationleads.org a top provider of loan modification leads. “Our customers are reporting that they have observed an increase in successful modifications in recent weeks.” He also mentioned that lead production has elevated as a outcome of greater consumer awareness of loan modification applications. A loan modification “lead” is a consumer initiated request for a consultation. Leadsnet Inc. has over 12,000 consultants and loan officers with active registrations.

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Government Programs

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The Federal Reserve announced a new “Homeownership Preservation Policy” which is aimed at borrowers who are 60 days or much more behind. This system is for loans that are owned by the Fed in its recent acquisitions of AIG and Bear Stearns. This system utilizes TARP funds which had been released at the finish of January.

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Hope For Home owners Loan System

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Congress created the HOPE for Property owners (H4H) program to help these who are 90 days or more behind in payments, refinance into much more reasonably priced, long term loans. H4H is an new mortgage designed to keep troubled borrowers in their homes. It is not a loan modification. This plan has been broadly characterized as a failure. The major reason the program did not catch on is that no new lenders want to make loans to borrowers who have a history of not paying and property that is declining in worth. Chairman Bernake in a recent speech acknowledged the applications shortcomings and called for modifications.

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FDIC Loan Modification

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The FDIC announced a plan late last year that promises to mitigate losses to the government and help individuals remain in their houses. This system contains money incentives to loan servicing companies and government share in potential losses.

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To qualify for the system you must have a loan that the FDIC administers and be at least 60 days behind in your mortgage payments ahead of the finish of 2009. This would apply to IndyMac Federal loans.

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The FDIC will restructure your payments so that they are no much more than 31% of your income. Interest prices can be set to 3% for 5 years. There is no principal reduction, rather the excess in the “cost-effective” loan balance and actual balance is added on to the loan at the finish or when the residence is sold.

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Fannie Mae and Freddie Mac Loan Modification

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The Fannie Mae and Freddie Mac plan is for homeowners that are at least 90 days behind in their payments and owe at least 90% of the residences value.

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With this program, the government will allow you to have a lower interest price and principal deferment. Debt ratio targets for this system is 38%. This means that your mortgage payment including tax and insurance can not be much more than 38% of your income. You should reside in the property and not be in bankruptcy.

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Wells Fargo, mentioned that they will be providing principle reduction in regions that have suffered the greatest market place declines. With their current acquisition of Wachovia, who created some of the most toxic “choose-a-payment and NINJA loans (No Income No Job No Assets) they join Bank of America who recently settled a multi-billion dollar law suit as a result of its obtain of Countrywide, who was the nations largest lender in the course of the bubble years.

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Consumers must be vigilant in negotiations with lenders. It is very best to get third party representation from an attorney, CPA or licensed mortgage broker that can negotiate on your behalf. If you can not afford professional representation, there are a lot of certified FHA neighborhood housing counselors that offer the service for totally free. Consumers can go to the Leadsnet inc. customer portal at http://www.loanfix.us for a totally free loan modification consultation.

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Springboard Provides Hope to Troubled Homeowners: Linked Press Reports on Foreclosure Prevention Counseling at Springboard

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Riverside, CA (PRWEB) March 7, 2009

Springboard Nonprofit Consumer Credit Management was the concentrate of a current story by John Mone of the Related Press, the story featuring foreclosure prevention counseling came on the heels of the Obama Administration and U.S. Department of Treasury’s Creating House Inexpensive system that offers assistance to 7 to 9 million property owners creating a great-faith work to make their mortgage payments.

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In the AP story Mone reported, “When it comes to foreclosure numbers, Riverside County California is pretty a lot in the leading ten in the United States. This is where the sub-prime mortgage meltdown struck deep.”

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With the U.S. unemployment price reaching its highest level in 25 years, Springboard is reporting a record number of counseling sessions in the regions of foreclosure prevention and credit and debt counseling. Throughout the nation, Springboard gives assistance with housing counseling, income and credit management via educational applications and complete counseling in both English and Spanish. Springboard is a HUD approved housing agency, a member of the National Foundation for Credit Counseling, and agency companion in the nationwide Homeownership Preservation Foundation’s Hope Hotline. “We encourage distressed home owners to attain out to their lenders and HUD approved housing counseling agencies like Springboard,” mentioned Melinda Opperman, vice president of neighborhood outreach at the Springboard housing and credit counseling agency. “We’re aware of situations on a everyday basis exactly where troubled home owners have been taken advantage of by paying upfront charges to organizations promising achievement for loan modifications and other workouts only to later understand no operate was performed and a lot damage has been completed. Negotiating loan workouts, options and solutions is anything lenders and non-profit housing counseling agencies offer you homeowners for cost-free,” mentioned Opperman.

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Springboard offers the following advice for customers facing foreclosure or other financial hardship.

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Open all mail promptly. Do not ignore the communication from your creditors or lenders.

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If you are having troubles producing your payments, call or write to your lender’s Loss Mitigation Division without having delay.

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Be prepared to explain your scenario and offer your lender with your monetary details.

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Do not pay funds upfront for a loan modification.

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Be wary of foreclosure rescue scam artists that claim to be helping you save your residence.

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Make contact with a HUD authorized housing counseling agency.

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In 2008, Springboard counseled almost 20,000 troubled home owners in California, and a lot more than 50,000 nationwide.

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About Springboard Nonprofit Consumer Credit Management&#13

SPRINGBOARD

Study Outlines Need for Enhanced COPD and Asthma Awareness, Allsup Reports

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Belleville, Ill. (PRWEB) June 25, 2013

Any individual with a single chronic lung illness such as chronic obstructive pulmonary disease (COPD) or asthma knows these critical respiratory circumstances can make each and every breath hard. But the struggle for thousands of Americans who have each COPD and asthma seems to be substantially much more serious, highlighting the significance of healthcare evaluation and awareness, according to Allsup, which has helped tens of thousands of folks acquire their Social Safety Disability Insurance coverage(SSDI) positive aspects.

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A recent study, reported in the journal Respiratory Medicine, showed that practically a single in 5, or 20 %, of individuals have COPD and overlapping complications with asthma. The study of three,885 people in between ages 40 and 80 identified these with each COPD and asthma knowledge a lot more wheezing, reduced breathing capacity, have trouble controlling symptoms and issues with physical activity, compared to those with just COPD.

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COPD involves conditions such as emphysema and chronic bronchitis, which can worsen over time. COPD is a leading of death in the United States, claiming much more than 120,000 lives each year, according to the National Heart, Lung, and Blood Institute (NHLBI). More than 12 million people in the U.S. have been diagnosed, and its estimated the exact same number are not conscious they have the situation. Asthma also is a critical chronic lung illness that impairs breathing. Far more than 3,000 folks each and every year die from asthma attacks, according to the institute.

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Respiratory situations such as COPD and asthma can be a severely disabling impairment, mentioned Ed Swierczek, senior claimant representative for Allsup. Not being in a position to breathe normally impacts every single component of a persons life, including their potential to work. It has a huge influence on top quality of life.

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Respiratory illnesses are a significant result in of extended-term disability. According to the Social Safety Administration (SSA), nearly 250,000 U.S. workers with respiratory illnesses obtain SSDI rewards. To be eligible for Social Security Disability Insurance coverage benefits, men and women must have a serious disability that is expected to last for a lot more than 12 months or is terminal. Individuals should have paid FICA payroll taxes to be eligible, and usually, have to have worked five out of the final 10 years. SSDI is a federally mandated insurance coverage plan overseen by the SSA.

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Allsup delivers the following suggestions when taking into consideration in search of SSDI positive aspects.

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1. Get your medical professional on board. Let health-related specialists know you are applying for SSDI and ask for their support. Treating physicians and providers are likely to be asked to supply medical records and their health-related opinion about the situation and capacity to function. Ask them to respond quickly to requests for information.

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2. Patience is critical. SSA normally requires 3 to six months to evaluation the initial application. The SSA denies most initial applications, so a lot of applicants need to file a disability appeal to get rewards. The national average wait time for a claim that has reached the hearing level is 373 days.

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3. Seek specialist SSDI aid. Representation from an advocate such as Allsup can make a significant difference in how rapidly an applicant gets an award and guarantees that certified applicants will get benefits. Allsup experts have hundreds of years of combined experience with the SSA and have helped a lot more than 200,000 people receive benefits much more quickly.

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If you have queries about your SSDI claim or disability appeal, call (800) 678-3276 for a totally free SSDI evaluation.

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ABOUT ALLSUP&#13

Allsup is a nationwide provider of Social Safety disability, veterans disability appeal, Medicare and Medicare Secondary Payer compliance solutions for men and women, employers and insurance coverage carriers. Founded in 1984, Allsup professionals deliver specialized solutions supporting people with disabilities and seniors so they may lead lives that are as financially secure and as healthy as feasible. The firm is based in Belleville, Ill., near St. Louis. For far more data, go to http://www.Allsup.com or go to Allsup on Facebook at http://www.facebook.com/Allsupinc.

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Revealing the Irony in Politics, in New Book “The Newshawk Reports”

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Rochester, NY (PRWEB) June 23, 2013

With a troubling economy, whispers of government cover-ups and increasing of national unemployment, Frederic Voss responded with a blog of social commentary.

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In The Newshawk Reports, Voss compiles his collection of stories, inspired by his weekly blogs from the past year. With a satirical edge that both the left and proper wing can appreciate, each and every weblog post tells a short story with an ironic twist, making an original and believed-provoking study.

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I can see the humor in mainly something, despite the fact that I see absolutely nothing funny in the way politicians are betraying the American individuals, says Voss. In The Newshawk Reports I offer you opinions on the nature of the ills that have befallen our country. I feel everybody is entitled to my opinion, specially correct-considering genuine Americans with a desire for unblemished truth.

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This skilled writer and seasoned watcher of the political scene injects his conservative view with a humorous-styled commentary. Discussing topics such as the present administration, the socialization of the country and the state of the education program, The Newshawk Reports illustrates how politicians and some media outlets are betraying the American men and women in expensive ways.

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The Newshawk Reports: the writings of a politically incorrect newsbird &#13

By Frederic Voss&#13

ISBN: 978-1-4771-3947-9&#13

Pages: 305&#13

Value: $ 19.95&#13

Available at http://www.xlibris.com, http://www.amazon.com, and http://www.barnesandnoble.com

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About the author&#13

Frederic Voss has been writing in his style of satire for a lot more than 25 years. He has been married to his wife, Mary for 41 years and they have three grown youngsters together. He at the moment lives in Western, N.Y.

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Ethicon Vaginal Mesh Lawsuits Continue, as Claims in New Jersey Litigation Exceed 3,000, Bernstein Liebhard LLP Reports

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New York, NY (PRWEB) June 21, 2013

Vaginal mesh lawsuit filings involving Ethicon Inc.s Gynecare pelvic mesh items continue to mount in a consolidated litigation underway in New Jerseys Atlantic County Superior Court, Bernstein Liebhard LLP reports. According to the most recent Case List issued by the Court, 3,017 claims have been filed in the New Jersey Ethicon litigation on behalf of alleged victims of vaginal mesh complications. Firm partner, Jeffrey S. Grand, is serving as Co-Liaison Counsel for this litigation. (In re: Pelvic Mesh/Gynecare Litigation, No. 6341-ten).

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It is not at all surprising that the vaginal mesh lawsuits filed in the New Jersey Ethicon litigation have reached this milestone. Practically two years following the FDA issued its final public overall health notification with regards to the risks linked with transvaginal mesh, we continue to hear from alleged victims of vaginal mesh complications on a standard basis, says Bernstein Liebhard LLP, a nationwide law firm representing victims of defective drugs and healthcare devices. The Firm continues to evaluate transvaginal mesh lawsuits on behalf of women allegedly injured by pelvic mesh products marketed by Ethicon, Inc. and other companies.

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Vaginal Mesh Complications&#13

Concerns over complications related with transvaginal mesh devices have been mounting considering that October 2008, when the U.S. Meals and Drug Administration (FDA) alerted the public that it had received much more than 1,000 adverse occasion reports involving individuals who had received the implants to treat pelvic organ prolapse and anxiety urinary incontinence. In July 2011, the FDA issued a second alert after such reports improved by five-fold, with the regulator now warning that the frequency of complications related with transvaginal prolapse repair was not rare. According to the agency, the most frequently reported vaginal mesh complications contain mesh erosion via the vaginal epithelium, pain, urinary difficulties and infection.*

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In March, the Plaintiff in the initial Ethicon mesh lawsuit to head to trial in the U.S. was awarded more than $ 11 million, like $ 7.76 million in punitive damages, after a jury in New Jersey Superior Court discovered that patients were not properly warned about the risks associated with the Gynecare Prolift device. Jeffrey S. Grand also served on the Plaintiffs trial group for this case. (Gross v. Gynecare Inc., Atl-L-6966-ten, Superior Court of Atlantic County, New Jersey)

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Mr. Grand is also serving as Co-Liaison Counsel for a consolidated litigation underway in Atlantic County Superior Court for lawsuits involving pelvic mesh manufactured by C.R. Bard Inc. (In re: Pelvic Mesh Litigation/Bard, No. L-6339-ten), and is a member of the Plaintiffs Steering Committees in four federal transvaginal mesh multi-district litigations underway in U.S. District Court, Southern District of West Virginia. These proceedings incorporate: In re: Boston Scientific Corp., Pelvic Repair Systems Goods Liability Litigation (MDL No. 2326) In re: C.R. Bard, Inc., In Re: American Healthcare Systems, Inc., Pelvic Repair Systems Products Liability Litigation (MDL No. 2325) In re: C.R. Bard, Inc., Pelvic Repair Systems Items Liability Litigation (MDL No. 2187) and In re: Ethicon, Inc., Pelvic Repair Systems Products Liability Litigation (MDL No. 2327). The 1st trial in that litigation, involving a C.R. Bard vaginal mesh lawsuit, is scheduled to begin on July 8, 2013.

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Alleged victims of vaginal mesh injuries might be eligible to seek compensation for health-related costs, discomfort and suffering and other damages. Learn a lot more about how to file a vaginal mesh lawsuit by going to Bernstein Liebhard’s internet site, or by contacting one particular of the Firms attorneys straight at 800-511-5092.

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*fda.gov/MedicalDevices/ProductsandMedicalProcedures/ImplantsandProsthetics/UroGynSurgicalMesh/default.htm

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About Bernstein Liebhard LLP &#13

Bernstein Liebhard LLP is a New York-primarily based law firm exclusively representing injured persons in complex person and class action lawsuits nationwide given that 1993, including those who have been harmed by dangerous drugs, defective medical devices and customer products. The firm has been named by The National Law Journal to the Plaintiffs Hot List, recognizing the prime plaintiffs firms in the nation, for the past ten consecutive years.

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Bernstein Liebhard LLP &#13

10 East 40th Street &#13

New York, New York 10016 &#13

(800) 511-5092

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Attorney Advertising.

Rottenstein Law Group LLP Comments on News Reports of Mirena IUD Side Effects

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New York, NY (PRWEB) June 19, 2013

As Mirena IUD lawsuits proceed in courts, the Rottenstein Law Group LLP highlights a recent news story from an NBC affiliate in Cleveland that features the critical alleged side effects of the hormone-based contraceptive device. The Rottenstein Law Group LLP publicizes this details to help these searching to file Mirena lawsuits and who are interested in understanding more about Mirena side effects.

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The U.S. Meals and Drug Administration has logged more than 70,000 complaints about the Mirena hormonal intrauterine device since the product very first went to marketplace in 2000, according to a June 17 NewsChannel five report.* Practically 5,000 of them have reported device migration, in which the IUD is displaced from its implantation website and moves to other parts of the uterus or beyond. The story even highlights a court case in which a woman alleges her Mirena IUD migrated into her rib cage.This can lead to the IUD becoming embedded in a womans uterine wall, the story stated. Far more than 1,300 ladies have complained about the IUD perforating their uteruses.

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The ladies in the NBC report affirm the issues of those who get in touch with us searching to file Mirena lawsuits, said Rochelle Rottenstein, principal of the Rottenstein Law Group LLP. As far more media interest is paid to the suffering, the far more these ladies feel empowered to investigate their alternatives for compensation.

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Much more than 60 Mirena lawsuits have been consolidated recently in New Jersey state court due to the fact they have widespread causes for suit, which makes it possible for for far more efficient pretrial proceedings, according to court documents in In re Mirena Litigation (Case No. 297, Superior Court of New Jersey, Bergen County). The plaintiffs allege the very same side effects as described in the NBC report.

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The Rottenstein Law Group LLP encourages those with the Mirena hormonal IUD to pay a visit to this web page to download a free informational brochure about the device and users eligibility to file a lawsuit.

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*nbcnews.com/id/52236628/#.UcC8cYletEI

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For the most recent news on defective medicines and health-related devices and related lawsuits, check out the Rottenstein Law Group LLPs Injury Lawyer Newswire at injurylawyernewswire.com. Readers can subscribe to the news web sites stories and videos to remain on leading of individual injury news.

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About THE ROTTENSTEIN LAW GROUP LLP&#13

The Rottenstein Law Group LLP is a New York-based firm that represents consumers nationwide in mass tort actions. The firm was founded by Rochelle Rottenstein, who has much more than two decades of experience as a lawyer, to represent consumers hurt by defective medical devices and medicines. (Lawyer marketing. Prior benefits do not assure a similar outcome.)

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Make contact with:&#13

The Rottenstein Law Group LLP&#13

Rochelle Rottenstein, Esq.&#13

321 W. 44th Street&#13

# 804&#13

New York NY 10036&#13

(212) 933-9500 (office phone)&#13

(212) 933-9980 (facsimile)&#13

rochelle (at) rotlaw (dot) com

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Mirena Lawsuit News: Bernstein Liebhard LLP Comments on Mounting Reports of Mirena Side Effects, Like Device Migration, Uterine Perforations

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New York, New York (PRWEB) June 18, 2013

As Mirena lawsuit claims continue to move forward in each state and federal court, a new report has revealed that that the IUD has been the subject of far more than 70,000 U.S. Meals &amp Drug Administration (FDA) adverse occasion reports since coming on the market in 2000. According to NewsChannel5 in Cleveland, Ohio, over 4.700 Mirena customers have reported device dislocation or migration to the FDA given that 2008, even though far more than 1,300 have reportedly seasoned uterine perforations due to Mirena.*

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We are not at all shocked by these numbers, as our Firm receives inquiries on a standard basis from females who have allegedly suffered uterine perforations, device migration, and other severe Mirena side effects. The injuries described in this report echo a lot of what we have heard from our own Mirena lawsuit consumers, says Bernstein Liebhard LLP, a nationwide law firm representing victims of defective drugs and medical devices. The Firm continues to provide free Mirena IUD lawsuit consultations to females who were allegedly harmed by this contraceptive device.

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Mirena Lawsuits&#13

According to the NewsChannel5 report, dozens of Mirena IUD lawsuits are at the moment pending in courts around the nation. Plaintiffs in these claims have allegedly suffered horrific injuries due to dislocation of the Mirena IUD, which includes instances where the device punctured the uterus and moved into the abdominal cavity and broken other organs. In one case, a plaintiff allegedly suffered a lacerated liver due to Mirena migration, while other people had been forced to undergo hysterectomies due to the fact of their injuries. 1 lady interviewed for the report even suffered permanent nerve damage right after undergoing surgery to take away a Mirena IUD that had migrated outside of her uterus. Regardless of these types of incidents, nevertheless, there is no indication that Bayer is organizing to concern a Mirena recall for the IUD.

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Court documents indicate that some 100 MIrena lawsuits are pending in a consolidated litigation underway in New Jersey Superior Court, Bergen County. A Case Management Conference has been scheduled for July 1st in that litigation. (In Re: Mirena Litigation Case No. 297) Meanwhile, at least 50 federally-filed Mirena side impact claims are also pending in a federal multidistrict litigation now underway in U.S. District Court, Southern District of New York. Even so, attorneys interviewed for the NewsChannel5 report predicted that hundreds of added Mirena IUD lawsuits would likely be filed in the near future. (In re: Mirena IUD Merchandise Liability Litigation, MDL No. 2434)

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Girls who suffered device migration, uterine perforations and other serious Mirena side effects could be entitled to compensation for their health-related costs, lost wages, pain and suffering and other damages. To understand much more about filing a Mirena lawsuit, please pay a visit to Bernstein Liebhard LLPs internet site. For far more data, please call 800-511-5092.

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*newsnet5.com/dpp/news/neighborhood_news/investigations/thousands-of-ladies-complain-about-harmful-complications-from-mirena-iud-birth-manage

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About Bernstein Liebhard LLP &#13

Bernstein Liebhard LLP is a New York-primarily based law firm exclusively representing injured persons in complex person and class action lawsuits nationwide because 1993, such as those who have been harmed by unsafe drugs, defective healthcare devices and consumer merchandise. The firm has been named by The National Law Journal to the Plaintiffs Hot List, recognizing the top plaintiffs firms in the nation, for the previous 10 consecutive years.

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Bernstein Liebhard LLP &#13

ten East 40th Street &#13

New York, New York 10016 &#13

800-511-5092

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Lawyer Marketing.