| Catalog Number |
CXI-2.3-14-135-ANG |
| Health Effect - Clinical Code |
No Known Impact Or Consequence To Patient (2692)
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| Date of Event |
05/26/2016
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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 cap(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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It was reported that the tip of the catheter split down the middle when crossing the total occlusion.A new cxi device was used to complete the procedure.There were no reported adverse effects to the patient as a result of the product problem.
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Search Alerts/Recalls
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