Drug recall
ALBON (sulfadimethoxine), Each bolus contains 5 g sulfadimethoxine, Bolus 5 g, 50 boluses, NADA #31-715, Not…
FDA recall event 57255 · Class III · Pfizer Inc.
Key facts
| Event ID | 57255 |
|---|---|
| Recall numbers | V-095-2011 |
| Recalling firm | Pfizer Inc. |
| Product type | Veterinary |
| Products | ALBON (sulfadimethoxine), Each bolus contains 5 g sulfadimethoxine, Bolus 5 g, 50 boluses, NADA #31-715, Not for Human Use, Distributed by Pfizer Animal Health, Div. of Pfizer Inc., NY, NY 10017, Made… |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The firm received two complaints that the product appeared moldy. Subsequent investigation confirmed the presence of mold (Penicillium citrinum) in retention samples for Lot PF98016. |
| Initiation date | Nov 10, 2010 |
| Termination date | Jun 12, 2012 |
| City | New York |
| State | NY |
| Country | United States |
| FEI number | 2416101 |
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