Class III · Lower riskActive recall
Acetaminophen Extra Strength 500 mg
Unlikely to cause harm — often a labeling or packaging issue.
Does this affect you?
Check your lot numberLot: KDT0224002A, Exp 09/30/2026
Where it was soldNationwide in the US
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
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
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
| Distributed by / for | Akron Pharma, Inc. |
| NDC | 71399-8022-01 |
Show the full FDA record
| Full product label | Acetaminophen Extra Strength 500 mg, 100 Tablets per bottle, Akron Pharma, Inc., 373 RT US 46 W Building E, Suite 117, Fairfield, NJ 07004, NDC 71399-8022-01. |
| Recalling firm | Akron Pharma, Inc. |
| Distribution | Nationwide in the US |
| Quantity | 768 bottles |
| Recall initiated | 2024-12-12 |
| Report date | 2025-01-22 |
| Recall completed | — |
| Recall number | D-0193-2025 |
| Classification | Class III |
| FDA status | Ongoing |
| Origin on file | Fairfield NJ 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.