| Model Number |
G23773 |
| Health Effect - Clinical Code |
No Known Impact Or Consequence To Patient (2692)
|
| Date of Event |
02/11/2016
|
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Type of Reportable Event
|
Malfunction
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|
Additional Manufacturer Narrative
|
|
This mdr is being filed after the associated complaint was reviewed under remediation protocol (b)(4), complaint/mdr retrospective review and remediation and reassessed as reportable.Additional complaint investigation and record remediation was not performed.
|
| |
|
Event or Problem Description
|
|
It was reported that during the tevar procedure, when the coda balloon catheter was used, the balloon ruptured after inflation.There was a delay reported and another device was used to complete the procedure successfully.
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Search Alerts/Recalls
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