Profarma Distributors recalls
Profarma Distributors has 5 recalls on record with the FDA and USDA, the earliest in 2016 and the latest reported on 29 Jun 2016. The most frequent reason is manufacturing (cgmp) deviations.
Total recalls5since 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 5 100%Class III 0 0%
Why profarma distributors is recalled
Product types
By year
All profarma distributors recalls, newest first
5 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | tabcin Noche recalled by Profarma Distributors | Profarma Distributors | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Vermox Tablets 100 mg recalled by Profarma Distributors | Profarma Distributors | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | tabcin Active M.R 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 |
| Drug | CLASS II | 1% Clotrimazol cream, 30 mg tube recalled by Profarma Distributors | Profarma Distributors | Manufacturing (CGMP) Deviations | Nationwide |
About this list
Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.