Amoxicillin and Clavulanate Potassium Tablets, USP, 500 mg/125 mg, in 20 count bottles, Rx Only, Manufactured in Austria by Sandoz Gmbh for Sandoz Inc. Princeton NJ NDC 0781-1831-20

FDA recall notice · announced June 7, 2017 · Sandoz

Class III FDA/FSIS Class III: use is not likely to cause adverse health consequences.

The product

Amoxicillin and Clavulanate Potassium Tablets, USP, 500 mg/125 mg, in 20 count bottles, Rx Only, Manufactured in Austria by Sandoz Gmbh for Sandoz Inc. Princeton NJ NDC 0781-1831-20

Reason for recall

Subpotent Drug; Clavulanic Acid

Notes

Distribution: NY, OH
Lot/code information: Lot FP8735, 8/2017
Quantity: 4,464 bottles
Status: Terminated
Products in this recall event:
- Amoxicillin and Clavulanate Potassium Tablets, USP, 500 mg/125 mg, in 20 count bottles, Rx Only, Manufactured in Austria by Sandoz Gmbh for Sandoz Inc. Princeton NJ NDC 0781-1831-20 (D-0868-2017)

Source: U.S. Food and Drug Administration public recall data. This page reports official records and is not legal, medical, or repair advice.