OEC Medical Systems, Inc OEC Miniview 6800 mobile fluoroscopic x-ray system, GE Healthcare, Surgery, Salt Lake City, Utah. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
OEC Miniview 6800 mobile fluoroscopic x-ray system, GE Healthcare, Surgery, Salt Lake City, Utah.
Brand
OEC Medical Systems, Inc
Lot Codes / Batch Numbers
Serial numbers in the range of 86-0032 to 86-2161
Products Sold
Serial numbers in the range of 86-0032 to 86-2161
OEC Medical Systems, Inc is recalling OEC Miniview 6800 mobile fluoroscopic x-ray system, GE Healthcare, Surgery, Salt Lake City, Utah. due to X-ray systems did not have the required labeling to indicate Air Kerma Rate and cumulative Air Kerma during fluoroscopic procedures. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
X-ray systems did not have the required labeling to indicate Air Kerma Rate and cumulative Air Kerma during fluoroscopic procedures
Recommended Action
Per FDA guidance
Consignees were notified by letter on 05/24/2007 and advised that a service representative would be contacting them for installation of the required label and to provide them with an update to their user's manuals.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AK, CA, CO, CT, FL, GA, ID, IN, KS, LA, MD, MI, MS, NY, OH, OK, OR, TX, VA
Page updated: Jan 10, 2026