Drug recall
VANTIN Tablets (cefpodoxime proxetil tablets), 200 mg, 20 tablet bottle, Rx only, Made in Belgium by Pharmacia…
FDA recall event 28195 · Class I · Graham Development Inc.
Key facts
| Event ID | 28195 |
|---|---|
| Recall numbers | D-133-4 |
| Recalling firm | Graham Development Inc. |
| Product type | Drugs |
| Products | VANTIN Tablets (cefpodoxime proxetil tablets), 200 mg, 20 tablet bottle, Rx only, Made in Belgium by Pharmacia & Upjohn N.V./S.A. Puurs-Belgium for Pharmacia & Upjohn Co., Kalamazoo, MI 49001 /… |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Mislabeled; bottles labeled as Vantin 200 mg may actually contain Lanoxin 0.25 mg |
| Initiation date | Jan 29, 2004 |
| City | Oneonta |
| Country | United States |
| FEI number | 3001868050 |
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