Recalls / Class II
Class IID-1042-2016
Product
VERMOX Tablets 500 mg, 1-count box, UPC 501109900596
- Affected lot / code info
- Lot # UJE 040; Exp. 02/17
Why it was recalled
CGMP Deviations
Recalling firm
- Firm
- Profarma Distributors LLC
- Notification channel
- Letter
- Type
- Voluntary: Firm initiated
- Address
- 4751 Poth Rd, N/A, Columbus, Ohio 43213-1331
Distribution
- Quantity
- 254 boxes (254 tablets)
- Distribution pattern
- Nationwide
Timeline
- Recall initiated
- 2016-05-11
- FDA classified
- 2016-06-17
- Posted by FDA
- 2016-06-29
- Terminated
- 2017-01-24
- Status
- Terminated
Source: openFDA Drug Enforcement endpoint. Recall record D-1042-2016. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.