Catalog Number 6007-616-000 |
Device Problem
Image Display Error/Artifact (1304)
|
Patient Problem
No Consequences Or Impact To Patient (2199)
|
Event Date 01/28/2019 |
Event Type
malfunction
|
Event Description
|
It was reported by the user facility that during a leg length verification post procedure, there was an inaccuracy by the device.The device reflected a length that was longer than the actual length.The exact inaccuracy was unknown, but less than 11mm.The procedure was completed successfully without a clinically significant delay; no adverse consequences or medical intervention were reported.
|
|
Manufacturer Narrative
|
Device evaluation: follow-up report submitted to document device evaluation results.
|
|
Event Description
|
It was reported by the user facility that during a leg length verification post procedure, there was an inaccuracy by the device.The device reflected a length that was longer than the actual length.The exact inaccuracy was unknown, but less than 11mm.The procedure was completed successfully without a clinically significant delay; no adverse consequences or medical intervention were reported.
|
|
Search Alerts/Recalls
|