Drug recall
Allura Xper series
FDA recall event 92855 · Class II · Philips Medical Systems Nederland B.V.
Key facts
| Event ID | 92855 |
|---|---|
| Recall numbers | Z-2402-2023, Z-2403-2023, Z-2404-2023 |
| Recalling firm | Philips Medical Systems Nederland B.V. |
| Product type | Devices |
| Products | Allura Xper series, Azurion, MultiDiagnost-Eleva |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | FDA Requested |
| Reason for recall | A foot switch pedal may get stuck in the active position when the user releases the pedal, resulting in the emission of unintended radiation |
| Initiation date | Jul 19, 2023 |
| Report date | Sep 13, 2023 |
| City | Eindhoven |
| Country | Netherlands |
| FEI number | 3000976525 |
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: