| Catalog Number |
CXI-2.6-18-90-P-NS-0 |
| Health Effect - Clinical Code |
No Known Impact Or Consequence To Patient (2692)
|
| Date of Event |
05/17/2016
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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), compliant/mdr retrospective review and remediation and reassessed as reportable.Additional complaint investigation and record remediation was not performed.
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|
Event or Problem Description
|
|
During the peripheral arterial occlusive disease procedure on the (b)(6) male patient, the chronic total occlusion wire perforated the device while devices went through the anterior tibial artery.No additional information available.
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Search Alerts/Recalls
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