| Catalog Number |
C-TQTS-2000 |
| 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
|
|
This mdr is being filed after the associated complaint was reviewed under remediation protocol cap008, 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 wire guide unraveled.No section of the device remained inside the patient's body.The patient did not require any additional procedures due to this occurrence.According to the initial reporter, the patient did not experience any adverse effects due to this occurrence.
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Search Alerts/Recalls
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