FDA Drug recall D-1500-2014
Losartan Potassium and Hydrochlorothiazide Tablets, USP 100 mg/25 mg, 90-tablets per bottle, Rx Only, Manufactured by: Jubilant Cadista Pha…
- FDA Drug
- Class II
- terminated
- Published 2014-08-06
On 2014-08-06 the FDA classified a Class II recall of Losartan Potassium and Hydrochlorothiazide Tablets, USP 100 mg/25 mg, 90-tablets per bottle, Rx Only, Manufactured by: Jubilant Cadista Pha… by Jubilant Cadista Pharmaceuticals, citing presence of Foreign Substance: Tablets may contain dark blemishes identified as stainless steel.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1500-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-07-11 |
| Published | 2014-08-06 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Jubilant Cadista Pharmaceuticals |
| Distribution | US |
Product
Losartan Potassium and Hydrochlorothiazide Tablets, USP 100 mg/25 mg, 90-tablets per bottle, Rx Only, Manufactured by: Jubilant Cadista Pharmaceuticals Inc., Salisbury, MD 21801, NDC # 59746-339-90
Reason
Presence of Foreign Substance: Tablets may contain dark blemishes identified as stainless steel.
Identifiers
| ndc | 59746-337-30 |
|---|---|
| ndc | 59746-337-90 |
| ndc | 59746-337-01 |
| ndc | 59746-337-10 |
| ndc | 59746-338-30 |
| ndc | 59746-338-90 |
| ndc | 59746-338-01 |
| ndc | 59746-338-10 |
| ndc | 59746-339-30 |
| ndc | 59746-339-90 |
| ndc | 59746-339-01 |
| ndc | 59746-339-10 |
| code_info | Lot #14P0292, Exp 04/2016 |
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-1500-2014%22
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