| Model Number |
42866 |
| Medical Device Problem Code |
Insufficient Device Problem Information (3190)
|
| Health Effect - Clinical Code |
Neurological Deficit/Dysfunction (1982)
|
| Date of Event |
03/05/2019
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Type of Reportable Event
|
Malfunction
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Additional Manufacturer Narrative
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If information is provided in the future, a supplemental report will be issued.
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Event or Problem Description
|
|
It was reported that after the valve was implanted, the valve was treated from 2.5 to 1.5 due to worsening of sensory symptoms.On (b)(6) 2019, the patient had a worsening of neurological symptoms.It was noted that there were no problems during the procedure.
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Search Alerts/Recalls
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