GEHC OEC 8800 Mobile Fluoroscopic X-ray System, GE Healthcare, Surgery, Salt Lake City, UT. Mobile fluoroscopic examination of human anatomy.
Reported: August 29, 2012 Initiated: October 19, 2007 #Z-2221-2012
Product Description
GEHC OEC 8800 Mobile Fluoroscopic X-ray System, GE Healthcare, Surgery, Salt Lake City, UT. Mobile fluoroscopic examination of human anatomy.
Reason for Recall
X-ray units did not meet manufacturer's specification for linearity.
Details
- Recalling Firm
- GE OEC Medical Systems, Inc
- Units Affected
- 175 units
- Distribution
- Worldwide Distribution - USA - Australia, Brazil, Cameroon, China, Colombia, Cyprus, The Czech Republic, Finland, France, Germany, Greece, Italy, Japan, Korea, Malaysia, The Netherlands, New Zealand, Norway, Russian Federation, Spain, Sweden, Taiwan, Turkey, UAE, UK, and Canada.
- Location
- Salt Lake City, UT
Frequently Asked Questions
What product was recalled? ▼
GEHC OEC 8800 Mobile Fluoroscopic X-ray System, GE Healthcare, Surgery, Salt Lake City, UT. Mobile fluoroscopic examination of human anatomy.. Recalled by GE OEC Medical Systems, Inc. Units affected: 175 units.
Why was this product recalled? ▼
X-ray units did not meet manufacturer's specification for linearity.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on August 29, 2012. Severity: Moderate. Recall number: Z-2221-2012.
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