The FDA announced a nationwide recall of Silintan joint pain supplements after testing found undeclared meloxicam, a ...
The FDA orders the recall of a nasal spray in the US after finding live microbes; immunocompromised patients are at greatest ...
A commonly used blood pressure medication has been recalled over fears that it may be cross-contaminated with another drug. Glenmark Pharmaceuticals Inc. has recalled more than 11,100 bottles of ...
Millions of Americans who rely on medication for attention deficit hyperactivity disorder (ADHD) may be affected by a new drug recall. Sun Pharmaceutical Industries has issued a voluntary, nationwide ...
The recall involved bottles manufactured by Greenville, South Carolina-based PAI Holdings, LLC, which was doing business as Pharmaceutical Associates Inc., per the report. The 100 mg/10 mg per 5 mL ...
The FDA said that over 140,000 bottles of the Lipitor generic potentially failed to meet "dissolution specifications." ...
The FDA recalled about 11,100 bottles of Ziac after finding trace contamination with ezetimibe. The recall includes 30-, 100-, and 500-count bottles with lot with expiration dates ranging from ...
Patients taking Ziac for blood pressure control should check their prescriptions immediately. Glenmark Pharmaceuticals has recalled several lots of the drug after testing revealed contamination with ...
A voluntary, nationwide recall has been issued for a common ADHD medication, lisdexamfetamine dimesylate The U.S. Food and Drug Administration has designated this a Class II recall, meaning it is ...
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