Catalog Number 6000-999-002 |
Device Problem
Disassembly (1168)
|
Patient Problem
No Known Impact Or Consequence To Patient (2692)
|
Event Date 11/30/2017 |
Event Type
malfunction
|
Event Description
|
It was reported that during set-up for a procedure conducted at the user facility the device had a spring fall out.A spring falling out during a surgical procedure could cause an infection.The device was not used after discovering the spring fell out.No known patient involvement or procedural delays were reported due to the incident.
|
|
Manufacturer Narrative
|
Device evaluation: follow-up report submitted to document device evaluation results.
|
|
Event Description
|
It was reported that during set-up for a procedure conducted at the user facility the device had a spring fall out.A spring falling out during a surgical procedure could cause an infection.The device was not used after discovering the spring fell out.No known patient involvement or procedural delays were reported due to the incident.
|
|
Search Alerts/Recalls
|