US Drug Recall Register
Class I · High risk Terminated Initiated Sep 29, 2022 (4 years ago)

Atenolol Tablets, USP, 25 mg, 1000-count bottle, Rx only, Manufactured by: ALPHAPHARM PTY…

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Label Mix - up; a bottle labeled as Atenolol 25mg Tablets contained Clopidogrel 75mg Tablets

What was recalled

Atenolol Tablets, USP, 25 mg, 1000-count bottle, Rx only, Manufactured by: ALPHAPHARM PTY LTD, Marketed by: GSMS, Incorporated, Camarillo, CA 93012, USA, NDC 60429-027-10

Recalling firm
Golden State Medical Supply Inc.
NDC code
60429-027-10
Origin
CA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0019-2023

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.

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