| Catalog Number |
CXI-2.6-18-150-P-NS-ANG |
| Health Effect - Clinical Code |
No Known Impact Or Consequence To Patient (2692)
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| Date of Event |
02/01/2016
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Type of Reportable Event
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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.
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Event or Problem Description
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During the paod (peripheral arterial vascular occlusive disease) procedure, the supporting catheter was fractured from the proximal when inserted into the patient.The physician used a new device for the procedure.There were no reported sections of the device left inside the patient¿s body or additional procedures as a result of this product problem.
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Search Alerts/Recalls
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