Table Patient Step on RFX/SFX, Legacy, and Precision 500D systems
Reported: June 7, 2017 Initiated: February 6, 2017 #Z-2179-2017
Product Description
Table Patient Step on RFX/SFX, Legacy, and Precision 500D systems
Reason for Recall
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.
Details
- Recalling Firm
- GE Healthcare, LLC
- Units Affected
- 2,380 (2,215 US; 165 OUS)
- Distribution
- 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.
- Location
- Waukesha, WI
Frequently Asked Questions
What product was recalled? ▼
Table Patient Step on RFX/SFX, Legacy, and Precision 500D systems. Recalled by GE Healthcare, LLC. Units affected: 2,380 (2,215 US; 165 OUS).
Why was this product recalled? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on June 7, 2017. Severity: Moderate. Recall number: Z-2179-2017.
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