Atlas FDA

RUS Tool Version Software

FDA device recall Z-1303-06 · posted 2006-09-30 · Terminated

Recall details

Recalling firm
GE OEC Medical Systems, Inc
Reason for recall
X-ray systems could provide output which exceeds the 20 R/minute limit.
Action taken
Consignees were notified by certified letter on 08/14-15/2006.
Root cause
Other
Status
Terminated
Product code
JAA
Quantity affected
121 units (US), 0 units (foreign)
Distribution
Worldwide
Date initiated
2006-08-16
Date posted
2006-09-30
Date terminated
2011-07-27
Location
Salt Lake City, UT

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