Drug recall
KIONEX¿ Sodium Polystyrene Sulfonate, USP, NDC 0574-2004-16, Rx Only, Net Weight 454 grams (1 lb), Packaged…
FDA recall event 52290 · Class II · Paddock Laboratories, Inc.
Key facts
| Event ID | 52290 |
|---|---|
| Recall numbers | D-1879-2009 |
| Recalling firm | Paddock Laboratories, Inc. |
| Product type | Drugs |
| Products | KIONEX¿ Sodium Polystyrene Sulfonate, USP, NDC 0574-2004-16, Rx Only, Net Weight 454 grams (1 lb), Packaged by: Paddock Laboratories, Inc., Minneapolis, MN 55427. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Impurity (ketones); causing odor |
| Initiation date | Apr 2, 2009 |
| Termination date | Mar 1, 2012 |
| City | Minneapolis |
| State | MN |
| Country | United States |
| FEI number | 2127022 |
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