Acetaminophen Extra Strength Tablets — Class I drug recall D-0631-2024
Terminated recall by A-S Medication Solutions LLC, reported 2024-08-14, distributed nationwide. Labeling: Label Mix-Up: Some bottles of Acetaminophen Extra Strength 500 mg tablets were incorrectly labeled w
| Recall number | D-0631-2024 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | A-S Medication Solutions LLC, Libertyville, IL, United States |
| Recall initiated | 2024-06-21 |
| Classified | 2024-08-08 |
| Reported by FDA | 2024-08-14 |
| Terminated | 2025-05-07 |
| Distributed | Nationwide (US) |
| Quantity | 429 bottles |
| Reason classes | labeling, potency |
| NDC | 50090-5313, 50090-5313-01, 50090-5313-02, 50090-5313-03, 50090-5313-04, 50090-5313-05 |
| Lot numbers | 4138197 |
| Expiration dates | 2025-10-31 |
Product
Acetaminophen Extra Strength Tablets, 500 mg each, 100 count bottles, Packaged By: A-S Medication Solutions, Libertyville, IL 60048. NDC: 50090-5313-2
Reason for recall
Labeling: Label Mix-Up: Some bottles of Acetaminophen Extra Strength 500 mg tablets were incorrectly labeled with the drug facts label for Aspirin 81 mg tablets.
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-0631-2024. 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.