PlainRecalls
FDA Devices Moderate Class II Terminated

Prestige II, Prestige SI, Prestige VH Prestige system is a new multi-purpose conventional and digital R/F remote controlled system.

Reported: June 19, 2019 Initiated: March 29, 2019 #Z-1751-2019

Product Description

Prestige II, Prestige SI, Prestige VH Prestige system is a new multi-purpose conventional and digital R/F remote controlled system.

Reason for Recall

There has been a reported incident of a Distar CRT monitor that has fallen off the monitor wall mount related to product aging.

Details

Recalling Firm
GE Healthcare, LLC
Units Affected
825 (38 US and 787 OUS) in total
Distribution
Worldwide Distribution: US (nationwide) to states of: AL, CA, CT, FL, GA, HI, IL, LA, MD, MI, MN, MO, NH, NY, OK, PA, TN, and VA; and countries of: Algeria, Argentina, Belgium, Bosnia & Herzegovina, Brazil, Bulgaria, Canada, China, Costa Rica, Cote D'Ivoire, Cyprus, Czech Republic, Egypt , France, French Polynesia, Germany, Greece, Guadeloupe, Guyana, Hungary, Italy, Japan, Korea, Lebanon, Mexico, Morocco, New Caledonia, Norway , Poland, Portugal, Russia, Saudi Arabia,Slovakia, Spain, Taiwan, Tunisia, Turkey, Ukraine, United Kingdom, Venezuela, and Vietnam.
Location
Waukesha, WI

Frequently Asked Questions

What product was recalled?
Prestige II, Prestige SI, Prestige VH Prestige system is a new multi-purpose conventional and digital R/F remote controlled system.. Recalled by GE Healthcare, LLC. Units affected: 825 (38 US and 787 OUS) in total.
Why was this product recalled?
There has been a reported incident of a Distar CRT monitor that has fallen off the monitor wall mount related to product aging.
Which agency issued this recall?
This recall was issued by the FDA Devices on June 19, 2019. Severity: Moderate. Recall number: Z-1751-2019.