FDA Drug recall D-0631-2024
Acetaminophen Extra Strength Tablets, 500 mg each, 100 count bottles, Packaged By: A-S Medication Solutions, Libertyville, IL 60048
- FDA Drug
- Class I
- terminated
- Published 2024-08-14
On 2024-08-14 the FDA classified a Class I recall of Acetaminophen Extra Strength Tablets, 500 mg each, 100 count bottles, Packaged By: A-S Medication Solutions, Libertyville, IL 60048 by A S Medication Solutions, citing 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.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0631-2024 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2024-06-21 |
| Published | 2024-08-14 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | A S Medication Solutions |
| Distribution | US |
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
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.
Identifiers
| ndc | 50090-5313-1 |
|---|---|
| ndc | 50090-5313-2 |
| ndc | 50090-5313-3 |
| ndc | 50090-5313-4 |
| ndc | 50090-5313-5 |
| code_info | Lot: 4138197; Exp 10/31/2025 |
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-0631-2024%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.