Amoxicillin 500mg 100 recall: CGMP Deviations
AMOXICILLIN 500MG 100; NDC/UPC 65862001401; RX; TABLETS
Why was Amoxicillin 500mg 100 recalled?
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
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?
SE5019062-A
- Product
- AMOXICILLIN 500MG 100; NDC/UPC 65862001401; RX; TABLETS
- Recalling firm
- Cardinal Health Inc.
- Quantity
- 373 bottles
- Distribution
- FL, GA, SC
- Recall date
- June 2, 2021
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)