Levothyroxine Sodium Tablets, USP, 150 mcg (0.0150 mg), 10… was recalled on July 13, 2026 in cooperation with the U.S. Food and Drug Administration because subpotent Drug.
Levothyroxine Sodium Tablets, USP, 150 mcg (0.0150 mg), 10 Tablets (10 x 1) unit dose blisters per carton, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN 46268 USA. Distributed by Cardinal Health, Dublin, OH 43017. NDC Bag: 55154-3563-0; NDC Blister: 0904-6956-61
Bag lot #: N02167A, Exp. Date 07/2026; Blister lot # N02167, Exp. Date 07/2026
Units affected: N/A
Where it was sold: Nationwide in the USA.
Compare the codes above against the label on your product — usually on the bottom, the back panel, or the packaging. If your unit isn't listed, it is not part of this recall.
Subpotent Drug
Class II means the product might cause a temporary or medically reversible health problem; the chance of serious harm is remote.
Stop using the product. Return it to the place of purchase for a refund, or dispose of it. Contact the recalling firm with questions.
Contact: Recalling firm: Major Pharmaceuticals
Not sure what you're entitled to? Read our guide: what to do if your product is recalled.
Always confirm details on the official notice from the U.S. Food and Drug Administration before acting.
View official notice →The control board inside the motor of the recalled air conditioners can fail, posing a risk of serious injury or death from fire and burn hazards.
The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI) and an adequate-length power cord, which may encourage use of an extension cord, posing serious risks of injury or death from shock and electrocution hazards.
The toys’ zipper contains levels of lead that exceed the standard set in the federal lead paint ban. Lead is toxic if ingested by young children and can cause adverse health issues.
Product Contamination. WASHINGTON, Sept. 06, 2026 – Prime Line Distributors, Inc., a Fort Lauderdale, Fla., firm, and Ferrarini USA, Inc., a Hoboken, N.J., firm, are recalling approximately 1,513 pounds of imported ready-to-eat (RTE) pork products that may be adulterated with Listeria monocytogenes ( Lm ), the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The imported RTE dr
Be the first to know when products like this are recalled. Free weekly digest, unsubscribe anytime.