Philips Incisive CT -Computed Tomography X-Ray System Model Number:… — Class II medical device recall Z-1585-2023
Ongoing recall by Philips North America, reported 2023-05-24, distributed nationwide. Multi-Function Foot Switch Unload Pedal Foot Entrapment-Pressing the Unload Pedal of the foot switch to perfor
| Recall number | Z-1585-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Philips North America, Cambridge, MA, United States |
| Recall initiated | 2023-03-20 |
| Classified | 2023-05-12 |
| Reported by FDA | 2023-05-24 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CL, CR, CZ, DE, GB, IL, IN, JP, LT, PH, PL, TH, ZA |
| UPC / GTIN / UDI-DI | 00884838105508 |
| Serial numbers | 34020, 34025, 34031, 34033OUS, 34042, 34047, 34062, 34064, 34066, 34092, 34107, 34111, 550007, 550008, 550009, 550010, 550011, 550014, 550018, 550021, 550036, 550038, 550040, 550059, 550068 and 21 more |
| Model numbers | 72814 |
Product
Philips Incisive CT -Computed Tomography X-Ray System Model Number: 72814
Reason for recall
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
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1585-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.