Model Number CI632 |
Device Problems
No Apparent Adverse Event (3189); Appropriate Term/Code Not Available (3191)
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Patient Problems
Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available (4581); No Clinical Signs, Symptoms or Conditions (4582)
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Event Type
Injury
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Manufacturer Narrative
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This report is submitted on september 15, 2023.
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Event Description
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Per the clinic, the device was explanted (date not reported).Additional information has been requested but has not been made available as of the date of this report.
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Manufacturer Narrative
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Correction: the initial mdr submitted on september 15, 2023, was filed inadvertently.No device explantation has occurred.This report is submitted on november 9, 2023.
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Search Alerts/Recalls
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