CLASS I Drug recall · Reported 2 Nov 2022 · FDA Enforcement Report
Atenolol Tablets, USP, 25 mg recalled by Golden State Medical Supply
Golden State Medical Supply is recalling Atenolol Tablets, USP, 25 mg, distributed nationwide in the US. The recall was initiated on 29 Sep 2022 and the FDA has classified it as Class I.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-0019-2023
- FDA event ID
- 90909
- Recalling firm
- Golden State Medical Supply, Camarillo, CA
- Brand
- Atenolol
- Manufacturer
- Golden State Medical Supply, Inc.
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 29 Sep 2022
- FDA classified
- 21 Oct 2022
- Reported
- 2 Nov 2022
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Drug class
- Blood Pressure Medication
Timeline
| 29 Sep 2022 | Recall initiated by company | |
| 21 Oct 2022 | Classified by FDA | +22 days |
| 2 Nov 2022 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Label Mix - up; a bottle labeled as Atenolol 25mg Tablets contained Clopidogrel 75mg Tablets
Product as listed by the FDA
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
Where it was distributed
USA Nationwide
Questions about this recall
Why was it recalled?
Label Mix - up; a bottle labeled as Atenolol 25mg Tablets contained Clopidogrel 75mg Tablets
Which lots are affected?
Lot #: GS046745, Exp 12/2023
Where was it sold?
USA Nationwide
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
More recalls from Golden State Medical Supply
All 55| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Prasugrel HCI, Tablets, USP, 10mg recalledPrasugrel | Golden State Medical Supply | Potency & Assay | Nationwide |
| Drug | CLASS II | Carbamazepine Tablets, USP, 200mg recalledCarbamazepine | Golden State Medical Supply | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Gsms Incorporated, Niacin Extended-release Tablets, USP, 1,000 MG recalledNiacin | Golden State Medical Supply | Potency & Assay | CA |
| Drug | CLASS III | Primidone Tablets, USP, 250 mg recalled by Golden State Medical SupplyPrimidone | Golden State Medical Supply | Other | Nationwide |
| Drug | CLASS III | Primidone Tablets, USP, 50 mg recalled by Golden State Medical SupplyPrimidone | Golden State Medical Supply | Other | Nationwide |
Other Atenolol recalls
All 5| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Atenolol Tablets, USP, 50 mg recalled by Legacy Pharmaceutical | Legacy Pharmaceutical Packaging | Packaging Defects | Nationwide |
| Drug | CLASS II | Atenolol Tablets, USP, 50 mg recalled by Zydus Pharmaceuticals USAAtenolol | Zydus Pharmaceuticals USA | Packaging Defects | Nationwide |
| Drug | CLASS II | ZyGenerics Atenolol Tablets, USP 25 mg recalledAtenolol | Zydus Pharmaceuticals USA | Potency & Assay | Nationwide |
| Drug | CLASS II | Atenolol Tablet, 12.5 mg (1/2 of 25 mg) recalled by Aidapak Services | Aidapak Services | Labeling Errors | 4 states |