Model Number L331 |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problems
Discomfort (2330); No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 10/19/2022 |
Event Type
Injury
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Manufacturer Narrative
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As no further information concerning this report is expected, our investigation is complete.This investigation will be updated should further information be provided.
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Event Description
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It was reported that this implantable pulse generator was repositioned for an unspecified reason.The device remains in service.No additional adverse patient effects were reported.
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Manufacturer Narrative
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As no further information concerning this report is expected, our investigation is complete.This investigation will be updated should further information be provided.
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Event Description
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It was reported that this implantable pulse generator was repositioned for an unspecified reason.The device remains in service.No additional adverse patient effects were reported.It was reported that this implantable pulse generator was repositioned due to patient discomfort.The device remains in service.No additional adverse patient effects were reported.
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Search Alerts/Recalls
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