VERMOX Tablets 500 mg recall: CGMP Deviations
VERMOX Tablets 500 mg, 1-count box, UPC 501109900596
Why was VERMOX Tablets 500 mg recalled?
CGMP Deviations
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?
Lot # UJE 040; Exp. 02/17
- Product
- VERMOX Tablets 500 mg, 1-count box, UPC 501109900596
- Recalling firm
- Profarma Distributors LLC
- Quantity
- 254 boxes (254 tablets)
- Distribution
- Nationwide
- Recall date
- June 29, 2016
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)