Vermox recalls
The FDA has published 2 recalls involving Vermox since 2016. The latest was reported on 29 Jun 2016. Most were for manufacturing (cgmp) deviations. Recalls usually affect specific lots, not every bottle on the market. Check the lot number on each recall page before acting.
Total recalls2since 2016
Last 12 months0reported
Class I00% of total
Ongoing0latest 29 Jun 2016
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 2 100%Class III 0 0%
Why vermox is recalled
Companies
By year
All vermox recalls, newest first
2 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Vermox Tablets 100 mg recalled by Profarma Distributors | Profarma Distributors | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Vermox Tablets 500 mg recalled by Profarma Distributors | Profarma Distributors | Manufacturing (CGMP) Deviations | Nationwide |
Should you stop taking Vermox?
Not on your own. Most recalls affect specific lots from one manufacturer, and stopping a prescription suddenly can be riskier than the defect. Check your lot number and NDC against the recall, then call the pharmacy that dispensed it for a replacement.