Drug recall
Intellivue iX Information Center Software - All PIIC iX Surveillance stations including: 866023 IntelliVue…
FDA recall event 79132 · Class II · Philips Electronics North America Corporation
Key facts
| Event ID | 79132 |
|---|---|
| Recall numbers | Z-0776-2018 |
| Recalling firm | Philips Electronics North America Corporation |
| Product type | Devices |
| Products | Intellivue iX Information Center Software - All PIIC iX Surveillance stations including: 866023 IntelliVue Info Center iX A.0 866117 PIIC Classic Upgrade 866389 IntelliVue Info Center iX B.0, C.0… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Once a surveillance station is restarted on January 1, 2018 or later, the station will be unable to perform patient discharge and transfer operations. Any subsequent attempt to perform these… |
| Initiation date | Jan 3, 2018 |
| Report date | Mar 7, 2018 |
| Termination date | Nov 14, 2019 |
| City | Andover |
| State | MA |
| Country | United States |
| FEI number | 1218950 |
At a glance
- 1–9 Products in this recall
- None 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: