Class II โ€” Potential Health Hazard

Potential health hazard โ€” use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Janumet (sitagliptin and metformin HCl) tablets Recalled by MERCK SHARP & DOHME CORP Due to Presence of foreign substance: Presence of stainless steel...

Date: March 31, 2022
Company: MERCK SHARP & DOHME CORP
Status: Terminated
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact MERCK SHARP & DOHME CORP directly.

Affected Products

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)

Quantity: 3600 cartons

Why Was This Recalled?

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

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About MERCK SHARP & DOHME CORP

MERCK SHARP & DOHME CORP has 2 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report