|
Model Number 21-2762 |
Device Problem
Fail-Safe Problem (2936)
|
Patient Problem
No Consequences Or Impact To Patient (2199)
|
Event Type
malfunction
|
Manufacturer Narrative
|
Customer has not yet returned the device to the manufacturer for device evaluation.When and if the device becomes available and is returned and evaluated, the manufacturer will file a follow-up report detailing the results of the evaluation.
|
|
Event Description
|
It was reported that during use of the listed device, the safety mechanism would not engage properly.No needle stick occurred.No adverse health outcome resulted from this event.
|
|
Search Alerts/Recalls
|
|
|