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U.S. Department of Health and Human Services

Class 2 Device Recall OEC 7600 Mobile Fluoroscopy System

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 Class 2 Recall
OEC 7600 Mobile Fluoroscopy System
see related information
Date Posted March 15, 2008
Recall Status1 Open
Recall Number Z-0716-2008
Recall Event ID 46349
Premarket Notification
510(K) Numbers
K000221  K970063 
Product Classification System, X-Ray, Fluoroscopic, Image-Intensified - Product Code JAA
Product GE Healthcare, Mobile Fluoroscopy X-Ray System, OEC Model 7600, GE Healthcare, Surgery, Salt Lake City, Utah.
Code Information All Serial Numbers
Recalling Firm/
GE OEC Medical Systems, Inc
384 Wright Brothers Dr
Salt Lake City, Utah 84116-2862
Manufacturer Reason
for Recall
Unnecessary operator exposure; X-ray machine may allow unwanted x-ray exposure to the operator.
FDA Determined
Cause 2
DESIGN: Device Design
Action On or about 9/6/2007, by Customer Notification Letter, users were notified that all affected units will be corrected by GE personnel with the addition of an additional shield.
Quantity in Commerce 157 units (Domestic), 142 units (Foreign)
Distribution Worldwide- USA including states of CO, DE, FL, NJ, MO, NY, PA, and TX (with VA and Military facilities) and countries of Australia, Austria, Belgium, Brazil, Chile, China, The Czech Republic, Denmark, France, Germany, Hungary, Israel, Italy, Norway, Spain, Sweden, Switzerland, Thailand, and The UK.
Total Product Life Cycle TPLC Device Report

1 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
510(K) Database 510(K)s with Product Code = JAA and Original Applicant = GE DEC MEDICAL SYSTEMS