Model Number 20E |
Device Problem
Failure to Deliver Shock/Stimulation (1133)
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Patient Problem
Ventricular Fibrillation (2130)
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Event Date 03/15/2021 |
Event Type
malfunction
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Manufacturer Narrative
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Physio-control contacted the customer to request additional information on the patient.The customer provided physio-control with the available patient information.Patient fields in which information is not provided were intentionally left blank.Physio-control continues to investigate the reported failure and will submit a supplemental report on this event to the fda as provided by 21 cfr 803.56.
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Event Description
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The customer contacted physio-control to report that their device failed to provide defibrillation this issue is patient related; however there was no adverse event reported.The customer indicated a back up device was used and the patient survived and is neurologically intact.
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Manufacturer Narrative
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Physio-control evaluated the customers device and was unable to duplicate or verify the reported issue.Proper device operation was observed through functional and performance testing.The device was returned to the customer for use.Root cause is unable to be determined.
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Event Description
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The customer contacted physio-control to report that their device failed to provide defibrillation.This issue is patient related; however there was no adverse event reported.The customer indicated a back up device was used and the patient survived and is neurologically intact.
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Search Alerts/Recalls
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