FDA Drug recall D-0015-2015
TOPIRAMATE Tablets 200 mg, 60 Tablet Bottles, Rx Only
- FDA Drug
- Class II
- terminated
- Published 2014-10-22
On 2014-10-22 the FDA classified a Class II recall of TOPIRAMATE Tablets 200 mg, 60 Tablet Bottles, Rx Only by Zydus Pharmaceuticals Usa, citing presence of Foreign Tablets: Presence of topiramate 100 mg tablets comingled with 200 mg tablets.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0015-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-09-15 |
| Published | 2014-10-22 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Zydus Pharmaceuticals Usa |
| Distribution | US |
Product
TOPIRAMATE Tablets 200 mg, 60 Tablet Bottles, Rx Only. Manufactured by Cadila Healthcare Ltd. Ahmedabad, India Distributed by: Zydus Pharmaceuticals USA Inc. Pennington, NJ USA 08534. NDC 68382-141-14.
Reason
Presence of Foreign Tablets: Presence of topiramate 100 mg tablets comingled with 200 mg tablets.
Identifiers
| ndc | 68382-138-14 |
|---|---|
| ndc | 68382-138-16 |
| ndc | 68382-138-01 |
| ndc | 68382-138-05 |
| ndc | 68382-139-14 |
| ndc | 68382-139-16 |
| ndc | 68382-139-01 |
| ndc | 68382-139-05 |
| ndc | 68382-140-14 |
| ndc | 68382-140-16 |
| ndc | 68382-140-01 |
| ndc | 68382-140-05 |
| ndc | 68382-141-14 |
| ndc | 68382-141-16 |
| ndc | 68382-141-01 |
| ndc | 68382-141-05 |
| code_info | Lot #: MN9828, Expiry: Oct 2015. |
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-0015-2015%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.