FDA Drug recall D-1042-2016
VERMOX Tablets 500 mg, 1-count box, UPC 501109900596
- FDA Drug
- Class II
- terminated
- Published 2016-06-29
On 2016-06-29 the FDA classified a Class II recall of VERMOX Tablets 500 mg, 1-count box, UPC 501109900596 by Profarma Distributors, citing CGMP Deviations.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1042-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-05-11 |
| Published | 2016-06-29 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Profarma Distributors |
| Distribution | US |
Product
VERMOX Tablets 500 mg, 1-count box, UPC 501109900596
Reason
CGMP Deviations
Identifiers
| upc | 501109900596 |
|---|---|
| code_info | Lot # UJE 040; Exp. 02/17 |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1042-2016%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.