Class II · ModerateActive recall
Amoxicillin and Clavulanate Potassium Tablets USP
Could cause temporary or reversible harm; serious harm is unlikely.
Does this affect you?
Check your lot numberLot #: 100047634 Exp. Date 4/2025; 35449379A, Exp. Date 7/2024
Where it was soldNationwide within the United States
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
Subpotent Drug
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 | Teva Pharmaceuticals USA, Inc., North Wales, PA 19454 |
| NDC | 0093-2272-34 |
Show the full FDA record
| Full product label | Amoxicillin and Clavulanate Potassium Tablets USP, Chewable 400mg/57mg, 20-count bottles, Rx only, Manufactured in Canada By: Teva Canada Limited, Toronto, Canada M1B 2K9; Manufactured For: Teva Pharmaceuticals USA, Inc., North Wales, PA 19454 NDC 0093-2272-34 |
| Recalling firm | Teva Pharmaceuticals USA, Inc |
| Distribution | Nationwide within the United States |
| Quantity | 34,448 bottles |
| Recall initiated | 2024-06-04 |
| Report date | 2024-06-26 |
| Recall completed | — |
| Recall number | D-0561-2024 |
| Classification | Class II |
| FDA status | Ongoing |
| Origin on file | Parsippany 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.