Model Number X SERIES |
Device Problem
Output Problem (3005)
|
Patient Problem
Cardiac Arrest (1762)
|
Event Date 02/26/2024 |
Event Type
malfunction
|
Manufacturer Narrative
|
Zoll medical corporation has received the product and will be providing a supplemental report when our investigation is completed.
|
|
Event Description
|
Complainant alleged that while attempting to defibrillate a patient (age & gender unknown), the device failed to charge to set energy.Complainant indicated that there was no adverse effect to the patient due to the reported malfunction.
|
|
Manufacturer Narrative
|
The device was returned to zoll medical corporation for evaluation.The customer's report was observed during review of the device data logs.However, the device was put through extensive testing without duplicating the report.The hex screws are retorqued as a precaution.The device was recertified and returned to the customer.The battery was not returned as part of this investigation.Analysis of reports of this type has not identified an increase in trend.
|
|
Search Alerts/Recalls
|