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GE Healthcare, LLC recalls Table Patient Step on RFX/SFX, Legacy, and Precision 500D systems
Recalled June 7, 2017 · FDA recall Z-2179-2017 · GE Healthcare
Hazard
Reported incidents of a patient step detaching from the table. A fall from a patient step detaching while in use could result in an injury to a patient or operator. · FDA Class II
Units
2,380 (2,215 US; 165 OUS)
Sold at
US: Nationwide including DC and Puerto Rico. OUS: Argentina, Australia, Brazil, Canada, Chile, Colombia, Costa Rica, Egypt, France, Germany, Greece, Honduras, Hungary, Indonesia, Ireland, Israel, Italy, Jamaica, Jordan, Kuwait, Libya, Malaysia, Malta, Mexico, Panama, Portugal, Russia, Saudi Arabia, Saudi Arabia, Slovakia, Spain, Thailand, United Arab Emirates, United Kingdom, Vietnam.
Description
Reported incidents of a patient step detaching from the table. A fall from a patient step detaching while in use could result in an injury to a patient or operator.
Product
Table Patient Step on RFX/SFX, Legacy, and Precision 500D systems
Manufacturer(s)
GE Healthcare, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →