RecallRadar

FDA Drug recall D-0019-2023

Atenolol Tablets, USP, 25 mg, 1000-count bottle, Rx only, Manufactured by: ALPHAPHARM PTY LTD, Marketed by: GSMS, Incorporated, Camarillo,…

On 2022-11-02 the FDA classified a Class I recall of Atenolol Tablets, USP, 25 mg, 1000-count bottle, Rx only, Manufactured by: ALPHAPHARM PTY LTD, Marketed by: GSMS, Incorporated, Camarillo,… by Golden State Medical Supply, citing label Mix - up; a bottle labeled as Atenolol 25mg Tablets contained Clopidogrel 75mg Tablets.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0019-2023
ClassificationClass I
Statusterminated
Initiated2022-09-29
Published2022-11-02
Last updated2026-09-13 11:52 UTC
CompanyGolden State Medical Supply
DistributionUS

Product

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

Reason

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

Identifiers

ndc60429-025-90
ndc60429-025-10
ndc60429-026-90
ndc60429-026-10
ndc60429-027-90
ndc60429-027-10
code_infoLot #: GS046745, Exp 12/2023

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0019-2023%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.