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Model Number 6371 |
Device Problem
Use of Device Problem (1670)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 02/13/2023 |
Event Type
Injury
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Event Description
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Related manufacturer reference number 1627487-2023-00879.It was reported that during an elective ipg replacement on (b)(6) 2023, the physician accidentally damaged both extensions and opted to explant and replace both extensions.Effective therapy was restored post operatively.
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Manufacturer Narrative
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Based on the information provided a device problem was not identified, as a result a conclusive cause for the reported patient effect, and the relationship to the product, if any, cannot be determined.
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Search Alerts/Recalls
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