FDA Drug Recalls

Recalls / Active ingredient / Amoxicillin

Amoxicillin

10 FDA drug recalls involving the active ingredient “Amoxicillin”.

DateClassProductFirm
2022-04-13Class IIAmoxicillin Capsules, USP, 500 mg, 100-count bottle, Rx only, MFG: Sandoz Pharma, NDC 0781-2613-01Mckesson Medical-Surgical Inc. Corporate Office
2022-01-26Class IIAMOXICILLIN Tablets, USP, 875MG, 20 Tablets, Rx Only, Manufactured by Sandoz GmbH for Sandoz Inc., Princeton, CARDINAL HEALTHCARE
2022-01-26Class IIAMOXICILLIN for Oral Suspension USP, 400MG/5ML, 100ML (when reconstituted), Manufactured In Canada By: TEVA CACARDINAL HEALTHCARE
2020-02-07Class IIAmoxicillin and Clavulanate Potassium Tablets, USP, 875 mg/125 mg, 20-count bottles, Distributed by: AurobindoAuroMedics Pharma LLC
2017-04-26Class IIIAmoxicillin and Clavulanate Potassium Tablets, USP, 500 mg/125 mg, in 20 count bottles, Rx Only, Manufactured Sandoz Inc
2016-11-04Class IIIAmoxicillin for Oral suspension, USP 400 mg/5 mL, 100 mL (when reconstituted), Rx only, Manufactured by: HikmaWest-Ward Pharmaceuticals Corp.
2016-06-24Class IIAmoxicillin for Oral Suspension USP, 400 mg/ 5 mL, 50 mL bottle, Rx only, Manufactured In Canada by: Teva CanaTeva North America
2013-06-18Class IIIAmoxicillin for Oral Suspension, USP 200 mg/5 mL, a) 75 mL bottle NDC 0093-4160-78 and b) 100 mL bottle NDC 00Teva Pharmaceuticals USA, Inc.
2013-04-26Class IIIAmoxicillin for Oral Suspension, USP 400mg/5mL, NDC 0093-4161-78 (75ml) and 0093-4161-73 (100mL)Teva Pharmaceuticals USA, Inc.
2013-04-18Class IIAmoxicillin Capsules USP 500 mg, Manufactured in Austria by Sandoz GmbH for Sandoz Inc., Princeton, NJ 08540, Sandoz Incorporated