US Drug Recall Register
Class II · Moderate risk Terminated Initiated Apr 1, 2022 (4 years ago)

Esomeprazole Magnesium Delayed-Release Capsules, USP 40 mg, packaged in Unit Dose Blister…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Failed Impurities/Degradation Specifications: OOS result was obtained for Any Other Individual Impurity at the 12M room temperature time point.

What was recalled

Esomeprazole Magnesium Delayed-Release Capsules, USP 40 mg, packaged in Unit Dose Blister Cards of 6 (10 cards of 6 Capsules each per carton), Rx only, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 USA. NDC 42292-010-16

Recalling firm
Mylan Institutional, Inc. (d.b.a. UDL Laboratories)
NDC code
42292-010-16
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0861-2022

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

Other Magnesium recalls

See all