Key Takeaway
VERMOX Tablets 100 mg; 6-count box, UPC 7501109900619 by Profarma Distributors LLC was recalled on May 11, 2016. The hazard: CGMP Deviations
VERMOX Tablets 100 mg; 6-count box, UPC 7501109900619
Description
VERMOX Tablets 100 mg; 6-count box, UPC 7501109900619
Hazard / Reason
CGMP Deviations
Class II: Product that may cause temporary or medically reversible health consequences.
Class II indicates the product may cause temporary or medically reversible health effects. The probability of serious harm is considered remote.
Products Affected
VERMOX Tablets 100 mg; 6-count box, UPC 7501109900619
DrugsCompany Information
Profarma Distributors LLC
Columbus, OH, United States
View all 5 recalls by Profarma Distributors LLC →Distribution
Nationwide
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Frequently Asked Questions
Is this recall still active?
Check the status badge at the top of this page. "Ongoing" means the recall is still active and you should follow the remedy instructions. "Completed" or "Terminated" means the recall process has concluded, though the safety issue remains relevant for any unrepaired products.
How do I check if my product is affected?
Compare the model number, lot code, serial number, or date range listed in the recall notice with the information on your product's label or packaging. For vehicles, check your VIN at NHTSA.gov/Recalls.
What remedy is available for this recall?
Check the remedy section above or contact the manufacturer directly for current remedy options.
Where can I find the original recall notice?
This recall was issued by FDA Drug. Visit the agency's official website for the original notice.