Tag Archives: Dietary Supplement Recall

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Actos, Avandia May Up Risk for Diabetic Macular Edema

A West Virginia man fitted with a metal-on-metal version of DePuy Orthopaedics’ Pinnacle Hip Implant System has filed suit against the company and its parent, Johnson & Johnson, alleging the device caused him to suffer pain and elevated cobalt levels. The Plaintiff is being represented by the national law ...

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Canadian Study Confirms Actos Bladder Cancer Risk

A new study conducted by Canadian researchers has found that users of the type 2 diabetes drug, Actos (pioglitazone), may face a higher risk of developing bladder cancer than first thought. The study, published in the British Medical Journal, found that taking Actos for two years doubles the likelihood ...

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E-cigarettes Could Increase Risk of Lung Infections

E-cigarettes Could Increase Risk of Lung Infections

New research suggests the liquid used in electronic cigarettes could increase the risk of viral lung infections, regardless of whether it contains nicotine.

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Actos Bladder Cancer Lawsuits Continue, New Complaint Filed by Tennessee Resident

Actos bladder cancer lawsuits continue, with a new complaint filed by a resident of Tennessee. The national law firm, Parker Waichman LLP, represents the Tennessee man who alleges that Actos caused his bladder cancer.

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Sleep Aids Can Increase Alzheimer’s Risk

A new study has found that over-the-counter sleeping aids and anti-allergy medicines can increase the risk of Alzheimer’s disease.

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1,000+ Australians Join DePuy ASR Hip Implant Class Action Lawsuit

A class action lawsuit filed in Australia over DePuy Orthopaedics’ recalled metal-on-metal ASR Hip Implants has signed up more than 1,000 plaintiffs. The attorneys representing the Australian ASR Hip Implant lawsuit plaintiffs recently told The Courier-Mail that damages in the lawsuit are expected to be worth more than $200 million. One ...

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Lawsuit Alleges Bi-Lateral DePuy ASR Hip Implant Resulted in Elevated Chromium and Cobalt Levels, Need for Revision Surgery

DePuy Orthopaedics and its parent, Johnson & Johnson, continue to be named in lawsuits by metal-on-metal hip replacement recipients who suffered severe injuries, including elevated chromium and cobalt levels, allegedly due to recalled ASR hip implant devices. Most recently, the national law firm of Parker Waichman LLP filed suit on ...

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Boston Scientific Transvaginal Mesh

Tennessee Woman Alleges Boston Scientific Transvaginal Mesh Product Caused Painful Injuries

More reports of painful injuries are being linked to transvaginal mesh. This time, a Tennessee woman has filed a lawsuit against Boston Scientific over its Advantage Transvaginal Mid-Urethral Sling System.

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West Virginia Man Claims Metal-on-Metal DePuy Pinnacle Hip Replacement Led to Pain, Elevated Cobalt Levels

A West Virginia man fitted with a metal-on-metal version of DePuy Orthopaedics’ Pinnacle Hip Implant System has filed suit against the company and its parent, Johnson & Johnson, alleging the device caused him to suffer pain and elevated cobalt levels. The Plaintiff is being represented by the national law ...

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British Recall of Smith & Nephew Renasys Wound Care System

British Recall of Smith & Nephew Renasys Wound Care System for Infection Risk

The MHRA announced the recall of Smith & Nephew Renasys wound care devices - risk of maceration, infection, loss of negative pressure, or unrecognized bleeding in wounds.

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Mojo Night Supplements Recalled for Unapproved Drug Ingredient

Mojo Night Supplements are being recalled for an unapproved drug ingredient, the U.S. Food & Drug Administration (FDA) just announced. Evol Nutrition Associates, Inc./Red Dawn of Kennesaw, Georgia said it is conducting a nationwide recall of all lots of two … Continue reading

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Body Basic Recalls Dietary Supplements for Dangerous Drug Ingredient

Body Basics Inc. just issued a recall of dietary supplements because they were manufactured with a dangerous drug ingredient, the U.S. Food &  Drug Administration (FDA) announced. The supplement manufacturer issued a nationwide recall of its ACTRA-Sx 500 Dietary Supplement … Continue reading

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FDA Issues Warning For Reumofan Dietary Supplement

The U.S. Food & Drug Administration (FDA) just issued a warning for Reumofan Plus dietary supplements due to the presence of potentially harmful pharmaceutical ingredients. Reumofan Plus is marketed as a “natural” dietary supplement for pain relief and other serious … Continue reading

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Shaping Beauty Recalls Weight Loss Pills

Shaping Beauty, Inc. of Southampton, Pennsylvania, has been informed by the U.S. Food and Drug Administration (FDA) < "http://www.yourlawyer.com/practice_areas/defective_drugs">that a weight loss dietary supplement it sold and marketed contains an undeclared drug ingredient. FDA lab analyses of the defective drugs … Continue reading

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