RecallDepth

GE OEC Brivo 865 Plus Mobile C-Arm X-Ray Product Used for general surgical applications and musculoskeletal procedures to visualize.

Company
Ge Oec Medical Systems, Inc
Recall Initiated
September 15, 2014
Posted
January 13, 2015
Terminated
May 20, 2015
Recall Number
Z-0841-2015
Quantity
61 units installed in US
Firm Location
Salt Lake City, UT

Reason for Recall

mA Accuracy may exceed the design and labeling specification of+ 10%. Per 1020.32(f): Deviation of x-ray tube potential and current from the indicated values shall not exceed the maximum deviation as stated by the manufacturer in accordance with 1020.30(h)(3).

Distribution

Worldwide Distribution

Lot / Code Info

GE OEC Brivo 865 Plus Serial Numbers:  B4S13011 B4S13012 B4S13016 B4S13018 B4S13020 B4S13029 B4S13031 B4S13035 B4S13038 B4S13043 B4S13054 B4S13056 B4S13059- B4S13061 B4S14002- B4S14004 B4S14007 B4S14015 B4S14016 B4S14022 B4S14022 B4S1403 3 B4S1403 4

Root Cause

Radiation Control for Health and Safety Act

Action Taken

Planned action(s) to repair defect or to bring product into compliance: GE Healthcare will, without charge, perform a mA calibration on all affected systems in the USA to bring the product back into compliance. The details of which will be included in a subsequent communication to customers or through a GE Healthcare field engineer site visit. Should customers have any questions or concerns regarding these corrections, please do not hesitate to contact the service team for further information at 800-874-7378 option 8.

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