Benicar 40mg 30 recall: CGMP Deviations
BENICAR 40MG 30; NDC/UPC 65597010430; RX; TABLETS
Why was Benicar 40mg 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?
1703296
- Product
- BENICAR 40MG 30; NDC/UPC 65597010430; RX; TABLETS
- Recalling firm
- Cardinal Health Inc.
- Quantity
- 75 bottles
- Distribution
- FL, GA, SC
- Recall date
- June 2, 2021
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)