Alert: Recall of prescription antidepressant
Pfizer Inc. has issued a recall of three lots of its antidepressant, Effexor XR (venlafaxine), after a pharmacist reported that one bottle of the medication contained a capsule of another product, ...

Recall Alert: L-Citrulline
The Food and Drug Administration (FDA) has received adverse event reports associated with L-citrulline repackaged and distributed by Medisca Inc. L-citrulline is used to treat certain urea cycle di...

Alert: Recall of Acetylcysteine
Ben Venue Laboratories, Inc. has issued a nationwide voluntary product recall of Acetylcysteine Solution 10%, 30 mL per vial. Lot 2005479 was recalled after a single visible glass particle was dis...

Alert: FDA to review diabetes medicine
The Food and Drug Administration (FDA) is investigating a possible risk of heart failure among patients with type 2 diabetes treated with saxagliptin, an active ingredient in the brand name medicin...

Recall of a single lot of Nifedipine
Greenstone LLC has recalled a single lot of Nifedipine, extended-release 90 mg tablets packaged in blister packs. Lot number V110079 has been recalled because an incorrect expiration date was print...