Continuous CT Fluoroscopy DVI Ceiling Mount — Class II medical device recall Z-0277-2022
Ongoing recall by Philips North America Llc, reported 2021-12-01, distributed nationwide. Significant wear of the Monitor Bracket Assembly shaft may go unrecognized could lead to the Monitor Bracket A
| Recall number | Z-0277-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Philips North America Llc, Cambridge, MA, United States |
| Recall initiated | 2021-05-01 |
| Classified | 2021-11-23 |
| Reported by FDA | 2021-12-01 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, DE, NL, SA |
| Quantity | 1 units |
| Reason classes | device malfunction |
| Serial numbers | 3202 |
Product
Continuous CT Fluoroscopy DVI Ceiling Mount - CCT Arm DVI Option - CT Vision ACQSIM CT System Number: 728209 Continuous CT (CCT) is a CT or PET/CT product option that enables physicians and radiologists to produce real-time CT images to facilitate image-guided surgery.
Reason for recall
Significant wear of the Monitor Bracket Assembly shaft may go unrecognized could lead to the Monitor Bracket Assembly detaching from the Suspension Arm, and resulting in injury to patient, operator, bystander, or service person located in the path of a falling part
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-0277-2022. 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.