Ondansetron HCL 4mg 30 recall: CGMP Deviations
ONDANSETRON HCL 4MG 30; NDC/UPC 65862018730; RX; TABLETS
Why was Ondansetron HCL 4mg 30 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?
ON0420015-A
- Product
- ONDANSETRON HCL 4MG 30; NDC/UPC 65862018730; RX; TABLETS
- Recalling firm
- Cardinal Health Inc.
- Quantity
- 1935 bottles
- Distribution
- FL, GA, SC
- Recall date
- June 2, 2021
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)