Drug recall
Apheresis Platelets
FDA recall event 81659 · Class III · The Blood Connection, Inc.
Key facts
| Event ID | 81659 |
|---|---|
| Recall numbers | B-0218-2019 |
| Recalling firm | The Blood Connection, Inc. |
| Product type | Biologics |
| Products | Apheresis Platelets |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Apheresis products, labeled with an incorrect volume, were distributed. |
| Initiation date | Jun 23, 2017 |
| Report date | Dec 26, 2018 |
| Termination date | Dec 20, 2018 |
| City | Piedmont |
| State | SC |
| Country | United States |
| FEI number | 1048067 |
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 · Source date: