Drug recall
Losartan Potassium and Hydrochlorothiazide Tablets, USP 50mg /12.5 mg, 1000-count bottle, Rx only…
FDA recall event 94592 · Class II · MACLEODS PHARMA USA, INC
Key facts
| Event ID | 94592 |
|---|---|
| Recall numbers | D-0498-2024 |
| Recalling firm | MACLEODS PHARMA USA, INC |
| Product type | Drugs |
| Products | Losartan Potassium and Hydrochlorothiazide Tablets, USP 50mg /12.5 mg, 1000-count bottle, Rx only, Manufactured for: Macleods Pharma USA, Inc. Princeton, NJ 08540, Manufactured by: Macleods… |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | Presence of foreign substance: plastic-like substance. |
| Initiation date | May 7, 2024 |
| Report date | May 22, 2024 |
| City | Princeton |
| State | NJ |
| Country | United States |
| FEI number | 3016842808 |
At a glance
- 1–9 Products in this recall
- None 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: