FDA Drug recall D-0627-2024
Acetaminophen, USP 500mg, Pain Reliever/Fever Reducer, Extra Strength, Rapid Release Gelcaps, packaged in a 225-count HDPE bottle, further…
- FDA Drug
- Class III
- terminated
- Published 2024-08-14
On 2024-08-14 the FDA classified a Class III recall of Acetaminophen, USP 500mg, Pain Reliever/Fever Reducer, Extra Strength, Rapid Release Gelcaps, packaged in a 225-count HDPE bottle, further… by Granules Consumer Health, citing label mix-up: Carton incorrectly labeled.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0627-2024 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2024-07-18 |
| Published | 2024-08-14 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | Granules Consumer Health |
| Distribution | IL |
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
Label mix-up: Carton incorrectly labeled.
Identifiers
| code_info | Lot #: 31670346AA, Exp 12/31/2026 |
|---|
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-0627-2024%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.