Drug recall
Misys Laboratory Blood Bank Module, Versions 6.1
FDA recall event 35065 · Class II · Misys Healthcare Systems
Key facts
| Event ID | 35065 |
|---|---|
| Recall numbers | B-1065-6 |
| Recalling firm | Misys Healthcare Systems |
| Product type | Biologics |
| Products | Misys Laboratory Blood Bank Module, Versions 6.1 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Defects in the design of software could result in data being out of sync with the accession number, patient and/or units displayed on the screen. |
| Initiation date | Mar 15, 2006 |
| Termination date | Apr 17, 2012 |
| 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