PlainRecalls
FDA Devices Moderate Class II Terminated

BrightView XCT , Model Number 882482

Reported: July 31, 2019 Initiated: June 10, 2019 #Z-2011-2019

Product Description

BrightView XCT , Model Number 882482

Reason for Recall

An issue with the handcontroller may result in either spontaneous uncommanded motions or continued motion after the buttons were released.

Details

Units Affected
427
Distribution
Worldwide Distribution - US Nationwide
Location
Cleveland, OH

Frequently Asked Questions

What product was recalled?
BrightView XCT , Model Number 882482. Recalled by Philips Medical Systems (Cleveland) Inc. Units affected: 427.
Why was this product recalled?
An issue with the handcontroller may result in either spontaneous uncommanded motions or continued motion after the buttons were released.
Which agency issued this recall?
This recall was issued by the FDA Devices on July 31, 2019. Severity: Moderate. Recall number: Z-2011-2019.