| Catalog Number |
C-UTLMY-501J-RSC-BH |
| Health Effect - Clinical Code |
No Known Impact Or Consequence To Patient (2692)
|
| Date of Event |
03/08/2016
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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.
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Event or Problem Description
|
|
It was reported the dilator could not be advanced through the catheter as the dilator tip was damaged and frayed.As a result, the procedure was completed with a different dilator.
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Search Alerts/Recalls
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