Recall archive / FDA drug enforcement
Acetaminophen, USP 500mg, Pain Reliever/Fever Reducer, Extra Strength, Rapid Release Gelcaps, packaged in a 225-count... — FDA record D-0627-2024
Reported terminated
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Jul 18, 2024. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- 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.
- Classification
- Class III
- Recalling firm
- Granules Consumer Health Inc.
- Quantity
- 21,192 Bottles
- Agency-reported status
- Terminated
- Source record identifier
- D-0627-2024
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | Lot #: 31670346AA, Exp 12/31/2026 |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
Recalled lot was distributed to one distributor in IL who may have further distributed the product to the retail level.
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
Dates in the source
- Report date
- Aug 14, 2024
- Recall initiation date
- Jul 18, 2024
- Center classification date
- Aug 6, 2024
- Termination date
- Feb 19, 2026
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.