Tag Archives: product recall

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Federal DePuy ASR Hip Implant Trials Likely to Start This Year

It looks as though the first trials in the DePuy ASR hip implant multidistrict litigation could begin sometime later this year. According to a report from Bloomberg News, during a status conference held yesterday in Florida, attorneys for both plaintiffs and the defense told U.S. District Judge David Katz that ...

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Stryker Metal Hip Implant Component Recall Bad News for Makers of Metal-on-Metal Hip Replacement Devices

Stryker’s recent recall of two metal hip implant components, the Rejuvenate Modular and ABG II modular-neck hip stems, may have dealt a serious blow to one of the key arguments medical device manufacturers have made to defend their metal-on-metal hip replacements. Facing thousands of lawsuits, the makers of ...

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Actos, Avandia May Up Risk for Diabetic Macular Edema

A newly published study is raising concerns that patients who take Actos or Avandia may face an increased risk of developing diabetic macular edema, an eye disorder that can result in vision loss. The study, published in the Archives of Internal Medicine, found that type 2 diabetics who use thiazolidinediones, ...

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Colorado Woman Sues American Medical Systems Over Transvaginal Mesh Injuries

Parker Waichman LLP, a national law firm, just filed a lawsuit on behalf of a Colorado woman allegedly injured by transvaginal mesh products manufactured by American Medical Systems, Inc. The suit was filed on May 21, 2012 in the U.S. District Court for the Northern District of California (Case No. ...

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Another Metal-on-Metal Hip Replacement Lawsuit Filed in DePuy ASR Hip Implant Litigation

A vital food safety program was saved from budget cuts this week, enabling the country’s largest—although considered by experts to be far too small—produce-safety testing program to continue.

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Bleeding Side Effects of Pradaxa, Xarelto Have Some Doctors Concerned

Some heart doctors are raising concerns about a new class of heart drugs that include Pradaxa. Recently, a number of doctors interviewed by Reuters said they were hesitant to prescribe Pradaxa, as well as another blood thinner called Xarelto, because of concerns regarding the risk of stroke, serious bleeding ...

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Actos Whistleblower Lawsuit Questions Avandia Researcher's Financial Ties to Takeda

A prominent researcher has been implicated in an alleged cover-up of Actos side effects, according to a report from TheHeart.org. An Actos whistleblower lawsuit unsealed earlier this year has alleged financial connections between the Cleveland Clinic’s Dr Steven Nissen and the maker of Actos “should be considered when analyzing Actos’s ...

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Cancer Groups Issue Statement for Regulation of E-cigarettes

Cancer Groups Issue Statement Calling for Research and Regulation of E-cigarettes

The American Society of Clinical Oncology & the American Association for Cancer Research are calling on the government to regulate e-cigarettes.

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Cancer Groups Call for E-cigarettes Regulation/Research

Two Leading Cancer Groups Issue Call for Regulation of E-cigarettes and Research on Health Risks

In a joint statement, the American Society of Clinical Oncology and the American Association for Cancer Research have called on the federal government to move quickly to regulate e-cigarettes and increase research on their health effects. These leading research and treatment organizations asked the Food and Drug Administration (FDA) to make ...

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Pradaxa Named in Most FDA Adverse Event Reports for Deaths, Hemorrhage, Kidney Failure and Stroke

The controversial blood thinner, Pradaxa, surpassed all other drugs monitored by the U.S. Food & Drug Administration (FDA) in adverse event reports made to the agency last year. According to the Institute for Safe Medicine Practices’ (ISMP) latest QuarterWatch report, Pradaxa also topped the list for reports of deaths, ...

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Personal Panic Devices Recalled Due to Malfunction

Personal Panic Devices Recalled Due to Malfunction

Interlogix is recalling 67,000 personal panic devices because they may fail to operate in case of an emergency. According to a recall alert posted on the U.S. Consumer Product Safety Commission (CPSC) website, “The wireless personal panic devices can fail … Continue reading

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Medtronic Recalls Thousands of Lots of Various Neurovascular Products

Medtronic Recalls Lots of Various Neurovascular Products

Medtronic PLC just recalled certain lots of four of its neurovascular products. The device maker noted that the recalled devices might lead to a thromboembolic event (blood clot) in patients. The recalled Medtronic neurovascular products are: Pipeline Embolization Device (1742 … Continue reading

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Class III Voluntary Recall Issued for High Blood Pressure Medication

Class III Recall Issued for High Blood Pressure Medication

As a result of a recent Enforcement Report of the U.S. Food and Drug Administration (FDA), Sun Pharma and Lupin  are recalling over 41.5 thousand drug bottles in the United States. Sun Pharmaceutical Industries Inc. is recalling 12,109 bottles of … Continue reading

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Lil’ Luxuries Infant Bath Tubs Recalled due to Risk of Serious Injury

Lil’ Luxuries Infant Bath Tubs Recalled due to Injury Risk

Approximately 86,000 Lil’ Luxuries Infant Bath Tubs with fabric slings have been recalled. The fabric slings on the recalled infant bath tubs may detach from the tub and pose a risk of impact injury or drowning, according to the United … Continue reading

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Evenflo Recalls 3-in-1 Combination Car Seats Due to Safety Risk

Evenflo Recalls Combination Car Seats Due to Safety Risk

A recall is being issued for Evenflo combination car seats due to safety risks. The recall, which affects 30,000 units, was launched following reports that children can loosen the safety harness on their own. If they can loosen the safety … Continue reading

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Black Forest Hams Recalled due to Possible Foreign Matter Contamination

Black Forest Hams Recalled due to Possible Contamination

The food company 502 Boundary Blvd. Inc., formerly known as Fletcher’s Fine Foods Ltd., has recalled approximately 8,700 pounds of ham products that may be contaminated with foreign matter, specifically rubber. The U.S. Department of Agriculture’s Food Safety and Inspection … Continue reading

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Gallo Meats LLC Recalls Sausage, Beef, and Lamb Products

Gallo Meats LLC Recalls Sausage, Beef, and Lamb Products

The United States Department of Agriculture’s (USDA) Food Safety and Inspection Service (FSIS) announced that Gallo Meats LLC of Colville, Washington, recalled Sausage, Beef, and Lamb products because they were produced without benefit of inspection. The recall was subsequently updated … Continue reading

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Potential Listeria Contamination Prompts Blue Bell to Recall Ice Cream

Listeria Contamination Prompts Blue Bell to Recall Ice Cream

A voluntary recall is being issued for Blue Bell Ice Cream produced in its Sylacauga, Alabama facility because there is a chocolate chip cookie dough ingredient supplied by a third party supplier, Aspen Hills, Inc., that may be contaminated with … Continue reading

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Medtronic Recalls Temporary Cardiac Lead Pacing Systems

Medtronic Recalls Temporary Cardiac Lead Pacing Systems

The Food and Drug Administration (FDA) has announced a Class II designation for a recall involving thousands of Medtronic temporary lead pacing systems because there is the potential for them to connect to a hazardous voltage. The recall involves 11,697 of … Continue reading

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Due to Fire Hazard, Nissan Recalls Maxima and Murano Models

Due to Fire Hazard, Nissan Recalls Maxima and Murano Models

Due to a potential fire risk, Nissan is recalling roughly 134,000 2016-2017 Maxima sedans, 2015-2017 Murano crossovers, and 2015-2016 Murano Hybrids. The recall only affects models equipped with Intelligent Cruise Control. According to Auto Blog, the recall is being issued … Continue reading

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