GE Healthcare Precision RXi 23A/32A Analog System
Reported: July 29, 2015 Initiated: June 12, 2015 #Z-2121-2015
Product Description
GE Healthcare Precision RXi 23A/32A Analog System
Reason for Recall
A reported incident of a monitor that fell from the suspension. A fall of a monitor could result in an injury to a patient or operator. Recall affects the single and dual LCD monitor suspensions used on Precision 500D Classical R & F system, Precision RXi 23A/32A Analog System, Precision RXi Digital system and Precision MPi fluoroscopic imaging systems.
Details
- Recalling Firm
- GE Healthcare
- Units Affected
- 788 (701 US; 87 OUS)
- Distribution
- Worldwide Distribution - US Nationwide Distribution including GU and DC., and to the countries of : Australia, Bulgaria, Canada, Chile, Dominican Republic, Germany, Ireland, Italy, Kuwait, Lebanon, Portugal, Romania, Russia, Saudi Arabia, Slovakia, Spain, Taiwan,Turkey, United Kingdom, Venezuela and Yemen.
- Location
- Waukesha, WI
Frequently Asked Questions
What product was recalled? ▼
GE Healthcare Precision RXi 23A/32A Analog System. Recalled by GE Healthcare. Units affected: 788 (701 US; 87 OUS).
Why was this product recalled? ▼
A reported incident of a monitor that fell from the suspension. A fall of a monitor could result in an injury to a patient or operator. Recall affects the single and dual LCD monitor suspensions used on Precision 500D Classical R & F system, Precision RXi 23A/32A Analog System, Precision RXi Digital system and Precision MPi fluoroscopic imaging systems.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on July 29, 2015. Severity: Moderate. Recall number: Z-2121-2015.
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