A trumpf medical service technician inspected the surgical light system and found the snap ring undone.The snap ring was replaced and the light is functioning as designed.A field corrective action has been initiated by trumpf medical and reported to the fda as a result of investigations into similar events (recall number z-563-2016).The investigations have found that improper installation or servicing of the circlip in this joint can result in the slipping down or falling of the spring arm and light head components.Based on this information, no further action is required.
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