PlainRecalls
FDA Drug Low Class III Terminated

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

Reported: June 7, 2017 Initiated: April 26, 2017 #D-0868-2017

Product Description

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

Details

Recalling Firm
Sandoz Inc
Units Affected
4,464 bottles
Distribution
NY, OH
Location
Princeton, NJ

Frequently Asked Questions

What product was recalled?
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. Recalled by Sandoz Inc. Units affected: 4,464 bottles.
Why was this product recalled?
Subpotent Drug; Clavulanic Acid
Which agency issued this recall?
This recall was issued by the FDA Drug on June 7, 2017. Severity: Low. Recall number: D-0868-2017.