FDA Drug recall D-0605-2017
ATENOLOL Tablets, USP, 50 mg, packaged in a) 100-count bottles (NDC 68382-023-01) and b) 1000-count bottles (NDC 68382-023-10), Rx only, Ma…
- FDA Drug
- Class II
- terminated
- Published 2017-03-29
On 2017-03-29 the FDA classified a Class II recall of ATENOLOL Tablets, USP, 50 mg, packaged in a) 100-count bottles (NDC 68382-023-01) and b) 1000-count bottles (NDC 68382-023-10), Rx only, Ma… by Zydus Pharmaceuticals Usa, citing presence of Foreign Tablets/Capsules: Customer complaint that a bottle of atenolol 50 mg Tablets USP contained a paroxetine 20 mg tablet.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0605-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-03-06 |
| Published | 2017-03-29 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Zydus Pharmaceuticals Usa |
| Distribution | US |
Product
ATENOLOL Tablets, USP, 50 mg, packaged in a) 100-count bottles (NDC 68382-023-01) and b) 1000-count bottles (NDC 68382-023-10), Rx only, Manufactured by: Cadila Healthcare Ltd., India; Distributed by: Zydus Pharmaceuticals USA Inc., Pennington, NJ 08534.
Reason
Presence of Foreign Tablets/Capsules: Customer complaint that a bottle of atenolol 50 mg Tablets USP contained a paroxetine 20 mg tablet.
Identifiers
| ndc | 68382-022-16 |
|---|---|
| ndc | 68382-022-01 |
| ndc | 68382-022-10 |
| ndc | 68382-022-40 |
| ndc | 68382-022-24 |
| ndc | 68382-023-16 |
| ndc | 68382-023-01 |
| ndc | 68382-023-10 |
| ndc | 68382-023-02 |
| ndc | 68382-023-40 |
| ndc | 68382-023-24 |
| ndc | 68382-024-16 |
| ndc | 68382-024-01 |
| ndc | 68382-024-10 |
| ndc | 68382-024-40 |
| code_info | Lot #: a) Z600724, Exp 04/18; Z600725, Exp 04/18 |
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-0605-2017%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.