Acetaminophen 325 mg tablets — Class III drug recall D-1352-2022
Terminated recall by Akron Pharma, Inc., reported 2022-08-24. Failed Tablet/Capsule Specifications: Imprint "AP 325" is missing from the tablet.
| Recall number | D-1352-2022 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Akron Pharma, Inc., Fairfield, NJ, United States |
| Recall initiated | 2022-08-04 |
| Classified | 2022-08-17 |
| Reported by FDA | 2022-08-24 |
| Terminated | 2023-12-04 |
| Quantity | 301,382 bottles |
| NDC | 71399-8024-01, 71399-8024-02 |
| Lot numbers | AKA10621, AKA20621, AKA30621, AKA40621, AKA50621, AKA60621, AKA70621, AKA80621, AKA90621, AKB10621, AKK2021, AKK30421, AKK40421, AKK50421, AKK60421, AKK70421, AKK80421, AKK90421, AKL10421, AKL10521, AKL20421, AKL20521, AKL30521, AKL40521, AKL50521, AKL60521, AKL70521, AKL80521, AKL90521, AKM10521, APR-24, AXA2001, AXA2002, AXA2003, AXA2004, AXA2005, AXA2006, AXA2007, AXA2008, AXA2009 and 8 more |
Product
Acetaminophen 325 mg tablets, packaged in a) 100-count bottle (NDC 71399-8024-01); b) 1000-count bottle (NDC 71399-8024-02), Akorn Pharma Manufactured for: Akorn Pharma, Inc., Fairfield, NJ
Reason for recall
Failed Tablet/Capsule Specifications: Imprint "AP 325" is missing from the tablet.
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-1352-2022. 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.