| Model Number |
G53024 |
| Health Effect - Clinical Code |
No Known Impact Or Consequence To Patient (2692)
|
| Date of Event |
12/19/2016
|
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Type of Reportable Event
|
Malfunction
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|
Additional Manufacturer Narrative
|
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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 evar procedure and use of a coda balloon catheter, the balloon would not dilate because of a pinhole in it.There were no patient injuries or additional procedures reported and another device was used to continue the procedure.
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Search Alerts/Recalls
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