GE Healthcare: Medical Device Recall in 2015 - (Recall #: Z-2121-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

GE Healthcare Precision RXi 23A/32A Analog System

Product Classification:

Class II

Date Initiated: June 12, 2015

Date Posted: July 29, 2015

Recall Number: Z-2121-2015

Event ID: 71574

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.

Status: Terminated

Product Quantity: 788 (701 US; 87 OUS)

Code Information:

Mfg Lot or Serial # 00000001386MC2 00000002109MC7 00000001010MC8 00000001337MC5 00000002212MC9 00000001720MC2 00000001098MC3 00000001454MC8 00000001082MC7 00000001266MC6 00000001656MC8 00000003661MC6

Distribution Pattern:

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.

Voluntary or Mandated:

Voluntary: Firm initiated