Our Posts

More than 700 Medtronic OmniaSecure defibrillation leads have been recalled over concerns about implantation difficulties and possible tissue trauma. Patients who suffer …

FDA records show a sharp increase in medical device recall listings, raising important questions about product safety, manufacturer accountability, and the legal …

FDA Class I Recall Raises Concerns About Insulin Overdoses, Dangerous Blood Sugar Changes, Hospital Patient Identification Errors, and Potential Medical Device Injury …

Class II Toothpaste Recall Raises Safety Concerns for Families Nationwide, Including Parents Who Purchased Children’s Fluoride Toothpaste What Parker Waichman LLP Found …

Nationwide Tirzepatide Injection Recall: Contamination Risks, Serious Injuries, and Potential Lawsuits What Parker Waichman LLP Found Nationwide recall: Apothecary Pharma recalled 22 …

FDA Class I Recall of Mercury-Contaminated Skin Lightening Creams Raises Serious Health Concerns and Potential Lawsuits Orbi 20 Whitening Cream and Omni …

Par Health Recalls Argatroban Injection Over Dangerous Particulate Contamination What Parker Waichman LLP Found Nationwide recall: Par Health recalled 22 lots of …

Federal investigations have raised concerns about experimental weight-loss peptides, contaminated injections, misleading advertising, and overseas manufacturers sending potentially dangerous products to American …

Federal regulators flag unapproved sexually transmitted infection treatments sold through Walmart’s online marketplace, raising concerns about delayed diagnoses, ineffective treatment, worsening infections, …

FDA Investigations Reveal Troubling Conditions at GLP-1 Drug Manufacturing Facilities What Parker Waichman LLP Found Based on the reported FDA inspection findings, …