Drug recall
Pooled Cryoprecipitated AHF
FDA recall event 87646 · Class II · BloodSource, Inc.
Key facts
| Event ID | 87646 |
|---|---|
| Recall numbers | B-0383-2021 |
| Recalling firm | BloodSource, Inc. |
| Product type | Biologics |
| Products | Pooled Cryoprecipitated AHF |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | Pooled Cryoprecipitated AHF that failed to meet QC specifications was distributed. |
| Initiation date | Feb 11, 2021 |
| Report date | Apr 21, 2021 |
| Termination date | Apr 14, 2021 |
| City | Mather |
| State | CA |
| Country | United States |
| FEI number | 3007101464 |
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 · Source date: