Drug recall
Apheresis Platelets, Irradiated
FDA recall event 74335 · Class II · Medic Inc
Key facts
| Event ID | 74335 |
|---|---|
| Recall numbers | B-0579-16, B-0580-16, B-0581-16 |
| Recalling firm | Medic Inc |
| Product type | Biologics |
| Products | Apheresis Platelets, Irradiated, Apheresis Platelets, Leukocytes Reduced, Apheresis Platelets, Leukocytes Reduced, Irradiated |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Apheresis Platelet products for which pH testing was invalid, were distributed. |
| Initiation date | May 4, 2016 |
| Report date | Jun 22, 2016 |
| Termination date | Jun 10, 2016 |
| City | Knoxville |
| State | TN |
| Country | United States |
| FEI number | 1077605 |
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: