Drug recall
Blood bank software Primary Application with Model numbers 5.4.0; 5.4.0.1; 5.4.0.2; and 5.4.1
FDA recall event 64560 · Class II · Blood Bank Computer Systems, Inc
Key facts
| Event ID | 64560 |
|---|---|
| Recall numbers | B-1344-13 |
| Recalling firm | Blood Bank Computer Systems, Inc |
| Product type | Biologics |
| Products | Blood bank software Primary Application with Model numbers 5.4.0; 5.4.0.1; 5.4.0.2; and 5.4.1 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood Bank Software, with a defect or glitch, was distributed. |
| Initiation date | Nov 1, 2012 |
| Report date | Apr 3, 2013 |
| Termination date | Jul 25, 2013 |
| City | Auburn |
| State | WA |
| Country | United States |
| FEI number | 1000221653 |
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: