Z-0279-2022 Class II Ongoing

Recalled by Philips North America Llc — Cambridge, MA

FDA device recall Z-0279-2022 was initiated by Philips North America Llc on May 1, 2021 and is designated Class II. 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, b… The recall status is ongoing. Affected quantity: 1 unit.

Recall Details

Product Type
Devices
Report Date
December 1, 2021
Initiation Date
May 1, 2021
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
1 unit

Product Description

Continuous CT Fluoroscopy DVI Ceiling Mount - CCT Arm DVI Option - TruFlight Select PET/CT System Number: 882438 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 Pattern

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

Code Information

Serial Number: 17006