FDA Drug recall D-1137-2017
Paroxetine tablets USP, 30mg, 30-count bottles, Rx Only, Manufactured by: Cadila Healthcare Ltd, Ahmedabad, India Distributed by: Zydus Pha…
- FDA Drug
- Class II
- terminated
- Published 2017-09-20
On 2017-09-20 the FDA classified a Class II recall of Paroxetine tablets USP, 30mg, 30-count bottles, Rx Only, Manufactured by: Cadila Healthcare Ltd, Ahmedabad, India Distributed by: Zydus Pha… by Zydus Pharmaceuticals Usa, citing presence of Foreign tablets/capsules: risperidone Tablets were found in bottle of paroxetine Tablets.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1137-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-08-18 |
| Published | 2017-09-20 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Zydus Pharmaceuticals Usa |
| Distribution | US |
Product
Paroxetine tablets USP, 30mg, 30-count bottles, Rx Only, Manufactured by: Cadila Healthcare Ltd, Ahmedabad, India Distributed by: Zydus Pharmaceuticals USA, Inc., Pennington, NJ 08534, NDC 68382-099-06, UPC 3 6838209906 8
Reason
Presence of Foreign tablets/capsules: risperidone Tablets were found in bottle of paroxetine Tablets
Identifiers
| upc | 368382099068 |
|---|---|
| ndc | 68382-097-16 |
| ndc | 68382-097-01 |
| ndc | 68382-097-05 |
| ndc | 68382-097-10 |
| ndc | 68382-097-06 |
| ndc | 68382-098-06 |
| ndc | 68382-098-16 |
| ndc | 68382-098-01 |
| ndc | 68382-098-05 |
| ndc | 68382-098-10 |
| ndc | 68382-099-06 |
| ndc | 68382-099-16 |
| ndc | 68382-099-01 |
| ndc | 68382-099-05 |
| ndc | 68382-099-10 |
| ndc | 68382-001-06 |
| ndc | 68382-001-16 |
| ndc | 68382-001-01 |
| ndc | 68382-001-05 |
| ndc | 68382-001-10 |
| ndc | 6838209906 |
| code_info | Lot #: Z701133, Exp 03/19 |
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-1137-2017%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.