# FDA recall Z-0277-2022

> **Philips North America Llc** · Class II · device recall initiated 2021-05-01.

## 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

## Distribution

US (nationwide) distribution to states of: CA, ME, TX and OUS (Foreign) to countries of:  Australia, Germany, Netherlands and Saudi Arabia.

## Key facts

- **Recall number:** Z-0277-2022
- **Recalling firm:** Philips North America Llc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2021-05-01
- **Report date:** 2021-12-01

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Cambridge, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0277-2022

## Citation

> AI Analytics. FDA recall Z-0277-2022. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-0277-2022. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*