Drug recall
Cefpodoxime Proxetil Tablets, USP, 200 mg, 20 Tablet Bottles, Rx Only. Manufactured in Austria by Sandoz GmbH…
FDA recall event 68360 · Class II · Sandoz, Inc
Key facts
| Event ID | 68360 |
|---|---|
| Recall numbers | D-1350-2014 |
| Recalling firm | Sandoz, Inc |
| Product type | Drugs |
| Products | Cefpodoxime Proxetil Tablets, USP, 200 mg, 20 Tablet Bottles, Rx Only. Manufactured in Austria by Sandoz GmbH for Sandoz Inc. Princeton, NJ 08540. NDC 0781-5439-20. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Presence of Foreign Substance: Presence of stainless steel particles. |
| Initiation date | May 22, 2014 |
| Report date | Jun 4, 2014 |
| Termination date | Feb 5, 2015 |
| City | Princeton |
| State | NJ |
| Country | United States |
| FEI number | 3006697677 |
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: