Class III · Lower riskRecall completed
Acetaminophen
Unlikely to cause harm — often a labeling or packaging issue.
Does this affect you?
Check your lot numberLot #: 31670346AA, Exp 12/31/2026
Where it was soldRecalled lot was distributed to one distributor in IL who may have further distributed the product to the retail level.
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.
What happened
Label mix-up: Carton incorrectly labeled.
What to do
- Check the lot number and expiry on your medicine against the recall above.
- Talk to your pharmacist or doctor before changing anything — don't stop on your own.
- Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).
Who makes it
Made byMade in India foreign manufacturer
| Distributed by / for | Walgreen Co., 200 Wilmot Rd, Deerfield, IL 60015 |
Show the full FDA record
| Full product label | 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 |
| Recalling firm | Granules Consumer Health Inc. |
| Distribution | Recalled lot was distributed to one distributor in IL who may have further distributed the product to the retail level. |
| Quantity | 21,192 Bottles |
| Recall initiated | 2024-07-18 |
| Report date | 2024-08-14 |
| Recall completed | 2026-02-19 |
| Recall number | D-0627-2024 |
| Classification | Class III |
| FDA status | Terminated |
| Origin on file | Manassas VA United States |
Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗
This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.