Drug recall
Cryoprecipitated AHF
FDA recall event 71626 · Class II · Medic Inc
Key facts
| Event ID | 71626 |
|---|---|
| Recall numbers | B-0715-15, B-0716-15 |
| Recalling firm | Medic Inc |
| Product type | Biologics |
| Products | Cryoprecipitated AHF, Plasma Cryoprecipitated Reduced |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, in which quality control and distribution of products did not meet specifications, were distributed. |
| Initiation date | May 12, 2015 |
| Report date | Aug 19, 2015 |
| Termination date | Aug 10, 2015 |
| 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: