Drug recall
Granisetron Hydrochloride Injection 1mg/mL For I.V. Use Only, Contains no Preservatives. Rx only, NDC number…
FDA recall event 50210 · Class II · Teva Pharmaceuticals USA, Inc.
Key facts
| Event ID | 50210 |
|---|---|
| Recall numbers | D-168-2009 |
| Recalling firm | Teva Pharmaceuticals USA, Inc. |
| Product type | Drugs |
| Products | Granisetron Hydrochloride Injection 1mg/mL For I.V. Use Only, Contains no Preservatives. Rx only, NDC number for individual vials is 0703-7871-01. NDC number for packages containing 10 vials is… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Exceeds pH Specifications |
| Initiation date | Oct 24, 2008 |
| Termination date | Aug 18, 2009 |
| City | Sellersville |
| State | PA |
| Country | United States |
| FEI number | 2517175 |
At a glance
- 1–9 Products in this recall
- 10–99 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