Drug recall
Misys Laboratory" Blood Bank and Blood Donor Modules V6.0.1
FDA recall event 45531 · Class II · Misys Healthcare Systems dba Misys Hospital Systems
Key facts
| Event ID | 45531 |
|---|---|
| Recall numbers | B-0293-08 |
| Recalling firm | Misys Healthcare Systems dba Misys Hospital Systems |
| Product type | Biologics |
| Products | Misys Laboratory" Blood Bank and Blood Donor Modules V6.0.1 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Misys identified that under certain scenarios the count for tests with unacceptable results is inaccurate. This could lead to: The QA failure, "Unit status updated to inventory with unacceptable… |
| Initiation date | Jun 27, 2007 |
| Termination date | Dec 5, 2011 |
| City | Tucson |
| State | AZ |
| Country | United States |
| FEI number | 1000306472 |
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