FDA Device recall Z-1586-2023
Philips Incisive CT -Computed Tomography X-Ray System Model Number: 72813
- FDA Device
- Class II
- ongoing
- Published 2023-05-24
On 2023-05-24 the FDA classified a Class II recall of Philips Incisive CT -Computed Tomography X-Ray System Model Number: 72813 by Philips North America, citing multi-Function Foot Switch Unload Pedal Foot Entrapment-Pressing the Unload Pedal of the foot switch to perform the unload function may cause entrapment of the operator's foot and….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1586-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-03-20 |
| Published | 2023-05-24 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Philips North America |
| Distribution | US |
Product
Philips Incisive CT -Computed Tomography X-Ray System Model Number: 72813
Reason
Multi-Function Foot Switch Unload Pedal Foot Entrapment-Pressing the Unload Pedal of the foot switch to perform the unload function may cause entrapment of the operator's foot and injury
Identifiers
| code_info | UDI-DI:(01)00884838085015(21) + Serial number US Serial Numbers: 33041, 500301, 500252. OUS Serial Numbers: 33040, 500408 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1586-2023%22
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