Class II · ModerateRecall completed
Extra-Strength Unaspirin caplet (Acetaminophen 500 mg) Bulk Container
Could cause temporary or reversible harm; serious harm is unlikely.
Does this affect you?
Check your lot numberProduct Codes: L207L Bulk Lots: 18K111, 19E104, 19F050
Where it was soldBulk product was distributed to 3 distributors who may have distributed finished product.
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
CGMP Deviations
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 | ULTRAtab Laboratories, Inc. |
| NDC | 62959-207-00 |
Show the full FDA record
| Full product label | Extra-Strength Unaspirin caplet (Acetaminophen 500 mg) Bulk Container, ULTRAtab Laboratories, Inc., Highland, NY NDC 62959-207-00 |
| Recalling firm | ULTRAtab Laboratories, Inc. |
| Distribution | Bulk product was distributed to 3 distributors who may have distributed finished product. |
| Quantity | 6,215,512 tablets |
| Recall initiated | 2022-01-26 |
| Report date | 2022-02-16 |
| Recall completed | 2025-01-07 |
| Recall number | D-0535-2022 |
| Classification | Class II |
| FDA status | Terminated |
| Origin on file | Highland NY 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.