Sandoz Inc recalls Amoxicillin and Clavulanate Potassium Tablets, USP, 500 mg/1
See all recalls from Sandoz Inc →Recalled 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
Hazard / Issue
Subpotent Drug; Clavulanic Acid
Issued by
FDA
Affected States: NY, OH
Lot/Code Info: Lot FP8735, 8/2017
✅ What Should You Do?
- 1Stop taking this medication and contact your doctor or pharmacist immediately.
- 2Do NOT flush medications down the drain — use an FDA-approved drug take-back program.
- 3Check the lot number on your bottle or packaging against the recalled lots listed above.
- 4Report adverse events to FDA MedWatch or call 1-800-FDA-1088.
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Search Amazon for Amoxicillin and Clavulanate Potassium →If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.
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