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FDAFDA · Food and drugs·Recall number D-0746-2022

Janumet (sitagliptin and metformin HCl) tablets, 50 mg/500 mg, 14-count bottle, packaged as 2 bottles per carton , Sample-Not For Sale, Rx Only, Manufactured for Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. Whitehouse Station, NJ 08889, USA, by Patheon Puerto Rico, Inc. Manati, Puerto Rico, 00674 Bottle (NDC 0006-0575-02), Carton (NDC 0006-0575-03)

Published April 13, 2022 · Recall initiated: March 31, 2022

Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

Presence of foreign substance: Presence of stainless steel particulates in tablets.

What to do

Voluntary: Firm initiated · Letter

Recall details

Brand
JANUMET
Manufacturer
MERCK SHARP & DOHME CORP
Distributor
Nationwide in the USA
UPC
0300060575617
Lot
Lot: U015824, Exp. 09/22.
Risk classification
Class II
Area (FDA)
drug
Country
United States

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