Acetaminophen 500 mg tablet packaged in a) 30-count bottles — Class II drug recall D-1005-2020
Terminated recall by H J Harkins Company Inc dba Pharma Pac, reported 2020-03-18, distributed nationwide. Presence of Foreign Tablets/Capsules: Complaint involving one Women's Prenatal dietary supplement tablet commi
| Recall number | D-1005-2020 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | H J Harkins Company Inc dba Pharma Pac, Grover Beach, CA, United States |
| Recall initiated | 2020-03-06 |
| Classified | 2020-03-12 |
| Reported by FDA | 2020-03-18 |
| Terminated | 2024-01-17 |
| Distributed | Nationwide (US) |
| Quantity | 11,973 tablets |
| Reason classes | potency |
| NDC | 52959-0002-30, 52959-0002-42, 52959-0002-45, 52959-0002-50 |
| Lot numbers | AE00M |
| Expiration dates | 2021-08 |
Product
Acetaminophen 500 mg tablet packaged in a) 30-count bottles ( NDC 52959-0002-30), b) 42-count bottles (NDC 52959-0002-42), c) 45-count bottles (NDC 52959-0002-45) and e) 50-count bottles (NDC 52959-0002-50) Repack: H.J. Harkins Co., Inc. Grover Beach, CA 93433
Reason for recall
Presence of Foreign Tablets/Capsules: Complaint involving one Women's Prenatal dietary supplement tablet commingled in a bottle of Extra Strength Acetaminophen 500 mg contents 1000 count bottle
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-1005-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.