Recall · FDA
Philips Medical Systems Nederland B.V.
Philips Medical Systems Nederland B.V. issued a Class II FDA recall (Z-2404-2023) initiated 2023-07-19: MultiDiagnost-Eleva
| Company | Philips Medical Systems Nederland B.V. |
|---|---|
| Recall number | Z-2404-2023 |
| Classification | Class II |
| Status | Ongoing |
| Category | Devices |
| Initiated | 2023-07-19 |
| Product | MultiDiagnost-Eleva |
| Reason | A foot switch pedal may get stuck in the active position when the user releases the pedal, resulting in the emission of unintended radiation |
FAQ
What did Philips Medical Systems Nederland B.V. recall?
MultiDiagnost-Eleva
Why was Philips Medical Systems Nederland B.V.'s product recalled?
A foot switch pedal may get stuck in the active position when the user releases the pedal, resulting in the emission of unintended radiation