Catalog Number 0703047000 |
Device Problems
Unintended Power Up (1162); Device Remains Activated (1525)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 10/11/2022 |
Event Type
malfunction
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Manufacturer Narrative
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A follow-up report will be filed once the quality investigation is complete.Awaiting device return.
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Event Description
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It was reported that during a procedure, the e-sep pencil was unintentionally activated.It was also reported that there were no adverse consequences and no medical intervention as a result of this event.It was not reported if there was a surgical delay.However, it was further reported that the procedure was completed successfully.
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Manufacturer Narrative
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H6: device code grid updated h6: the quality investigation is complete.
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Event Description
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It was reported that during a procedure, the e-sep pencil was unintentionally activated.It was also reported that there were no adverse consequences and no medical intervention as a result of this event.It was not reported if there was a surgical delay.However, it was further reported that the procedure was completed successfully.
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Search Alerts/Recalls
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