Drug recall
CPDA-1 Blood-Pack, Triple for 450 mL blood; Baxter Healthcare Corporation, Fenwal Division, Deerfield, IL…
FDA recall event 25065 · Class II · Baxter Healthcare Corp./Fenwal
Key facts
| Event ID | 25065 |
|---|---|
| Recall numbers | B-0482-3, B-0483-3, B-0484-3, B-0485-3, B-0486-3, B-0487-3, B-0488-3 |
| Recalling firm | Baxter Healthcare Corp./Fenwal |
| Product type | Biologics |
| Products | CPDA-1 Blood-Pack, Triple for 450 mL blood; Baxter Healthcare Corporation, Fenwal Division, Deerfield, IL 60015, CPDA-1 Blood-Pack, Triple, for 500 mL blood; Baxter Healthcare Corporation, Fenwal Division, Deerfield, IL 60015, CPDA-1 Blood-Pack, Triple, for 500 mL blood; Baxter Healthcare Corporation, Fenwal DIvision, Deerfield, IL 60015, CPD Blood-Pack, Quadruple, for 500 mL blood; Baxter HEalthcare Corporation, Deerfield, IL 60015, CPD Blood-Pack, Quadruple for 500 mL blood; Baxter Healthcare Corporation, Fenwal Division, Deerfield, IL 60015 and 2 more |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The PL 732 Platelet container may split during component preparation. |
| Initiation date | Nov 7, 2002 |
| City | Deerfield |
| Country | United States |
| FEI number | 1420141 |
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