Drug recall
Losartan Potassium and Hydrochlorothiazide Tablets, USP 100 mg/25 mg, 90-tablets per bottle, Rx Only…
FDA recall event 68776 · Class II · Jubilant Cadista Pharmaceuticals Inc.
Key facts
| Event ID | 68776 |
|---|---|
| Recall numbers | D-1500-2014 |
| Recalling firm | Jubilant Cadista Pharmaceuticals Inc. |
| Product type | Drugs |
| Products | 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 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Presence of Foreign Substance: Tablets may contain dark blemishes identified as stainless steel. |
| Initiation date | Jul 11, 2014 |
| Report date | Aug 6, 2014 |
| Termination date | Sep 15, 2016 |
| City | Salisbury |
| State | MD |
| Country | United States |
| FEI number | 1000513046 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: