Amoxicillin and Clavulanate Potassium Tablets recall: Subpotent
Amoxicillin and Clavulanate Potassium Tablets, USP, 500 mg/125 mg, in 20 count bottles, Rx Only, Manufactured in Austria by Sandoz Gmbh for Sandoz…
Why was Amoxicillin and Clavulanate Potassium Tablets recalled?
Subpotent Drug; Clavulanic Acid
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot FP8735, 8/2017
- 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…
- Recalling firm
- Sandoz Inc
- Quantity
- 4,464 bottles
- Distribution
- NY, OH
- Recall date
- June 7, 2017
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)