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
Reported: June 26, 2024 Initiated: June 4, 2024 #D-0561-2024
Product Description
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
Reason for Recall
Subpotent Drug
Details
- Recalling Firm
- Teva Pharmaceuticals USA, Inc
- Units Affected
- 34,448 bottles
- Distribution
- Nationwide within the United States
- Location
- Parsippany, NJ
Frequently Asked Questions
What product was recalled? ▼
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. Recalled by Teva Pharmaceuticals USA, Inc. Units affected: 34,448 bottles.
Why was this product recalled? ▼
Subpotent Drug
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on June 26, 2024. Severity: Moderate. Recall number: D-0561-2024.
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