| Model Number |
G15145 |
| Health Effect - Clinical Code |
No Known Impact Or Consequence To Patient (2692)
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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 capa (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
|
|
The complainant reported that the filiform double pigtail ureteral stent broke upon insertion during a cardiovascular procedure.There were no reports of any sections of the device remaining within the patient or any serious injuries to the patient.
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Search Alerts/Recalls
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