Drug recall
Apheresis Platelets, Leukocytes Reduced
FDA recall event 75216 · Class II · BloodSource, Inc.
Key facts
| Event ID | 75216 |
|---|---|
| Recall numbers | B-0097-2017 |
| Recalling firm | BloodSource, Inc. |
| Product type | Biologics |
| Products | Apheresis Platelets, Leukocytes Reduced |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Platelet products, not prepared in accordance with specifications, were distributed. |
| Initiation date | Aug 18, 2016 |
| Report date | Nov 2, 2016 |
| Termination date | Oct 27, 2016 |
| 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: