Drug recall
Fosinopril Sodium and Hydrochlorothiazide Tablets, 10 mg/12.5 mg, Rx Only, 100 Tablets, Sandoz Inc. Princeton…
FDA recall event 66554 · Class II · Sandoz Inc
Key facts
| Event ID | 66554 |
|---|---|
| Recall numbers | D-393-2014 |
| Recalling firm | Sandoz Inc |
| Product type | Drugs |
| Products | Fosinopril Sodium and Hydrochlorothiazide Tablets, 10 mg/12.5 mg, Rx Only, 100 Tablets, Sandoz Inc. Princeton, NJ 08540 ---NDC 0185-0341-01, |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Subpotent; Hydrochlorothiazide at the 9 month time point. |
| Initiation date | Oct 11, 2013 |
| Report date | Jan 8, 2014 |
| Termination date | Mar 5, 2015 |
| City | Wilson |
| State | NC |
| Country | United States |
| FEI number | 3000210731 |
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: