Drug recall
Losartan Potassium Tablets, USP, 25 mg, 1000 film coated tablets per bottle, Rx Only, Manufactured by: Vivimed…
FDA recall event 92584 · Class II · Strides Pharma Inc.
Key facts
| Event ID | 92584 |
|---|---|
| Recall numbers | D-0895-2023 |
| Recalling firm | Strides Pharma Inc. |
| Product type | Drugs |
| Products | Losartan Potassium Tablets, USP, 25 mg, 1000 film coated tablets per bottle, Rx Only, Manufactured by: Vivimed Life Sciences Private Limited, Plot No. 101, 102, 107 & 108, SIDCO Pharmaceutical… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | Presence of Foreign Substance: Presence of a small piece of blue plastic embedded in the tablet. |
| Initiation date | Jun 26, 2023 |
| Report date | Jul 12, 2023 |
| Termination date | May 15, 2024 |
| City | East Brunswick |
| State | NJ |
| Country | United States |
| FEI number | 3011707936 |
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: