Recall Z-0426-2015— GE Inspection Technologies, LP
Class II · Terminated
Class II FDA medical device recall by GE Inspection Technologies, LP, initiated 2014-11-10, terminated 2015-06-29. FDA's recall record names no specific 510(k) clearance for this event. Product: GE Cabinet X-ray systems. Reason: GE discovered these cabinet x-ray systems' potential failure to comply with the Cabinet X-ray System performance standards..
- Recalling firm
- GE Inspection Technologies, LP
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2014-11-10
- Terminated
- 2015-06-29
- Firm location
- Lewistown, PA, United States
Product description
GE Cabinet X-ray systems
Reason for recall
GE discovered these cabinet x-ray systems' potential failure to comply with the Cabinet X-ray System performance standards.
Data sourced from openFDA. This site is unofficial and independent of the FDA.