Drug recall
ProxiDiagnost N90, UDI 706100
FDA recall event 85603 · Class II · Philips North America, LLC
Key facts
| Event ID | 85603 |
|---|---|
| Recall numbers | Z-2256-2020 |
| Recalling firm | Philips North America, LLC |
| Product type | Devices |
| Products | ProxiDiagnost N90, UDI 706100 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The thermo switches in the three-phase transformer, which normally aid in powering down the System Power Distribution Unit, may be incorrectly installed and not working. If the transformer overheats… |
| Initiation date | Apr 23, 2020 |
| Report date | Jun 10, 2020 |
| Termination date | Mar 30, 2023 |
| 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: