Acetaminophen — Class III drug recall D-0627-2024
Terminated recall by Granules Consumer Health Inc., reported 2024-08-14, distributed in IL. Label mix-up: Carton incorrectly labeled.
| Recall number | D-0627-2024 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Granules Consumer Health Inc., Manassas, VA, United States |
| Recall initiated | 2024-07-18 |
| Classified | 2024-08-06 |
| Reported by FDA | 2024-08-14 |
| Terminated | 2026-02-19 |
| Distributed | IL |
| Quantity | 21,192 bottles |
| Reason classes | labeling |
| Lot numbers | 31670346AA |
| Expiration dates | 2026-12-31 |
Product
Acetaminophen, USP 500mg, Pain Reliever/Fever Reducer, Extra Strength, Rapid Release Gelcaps, packaged in a 225-count HDPE bottle, further packaged in a carton, Distributed by Walgreen Co., 200 Wilmot Rd, Deerfield, IL 60015, Made in India
Reason for recall
Label mix-up: Carton incorrectly labeled.
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-0627-2024. 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.