VERMOX Tablets 100 mg recall: CGMP Deviations
VERMOX Tablets 100 mg; 6-count box, UPC 7501109900619
Why was VERMOX Tablets 100 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 # UPE187; Exp. 08/17
- Product
- VERMOX Tablets 100 mg; 6-count box, UPC 7501109900619
- Recalling firm
- Profarma Distributors LLC
- Quantity
- 163 boxes (978 tablets)
- Distribution
- Nationwide
- Recall date
- June 29, 2016
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)