Model Number MSERIES |
Device Problem
Inaccurate Synchronization (1609)
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Patient Problem
No Known Impact Or Consequence To Patient (2692)
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Event Date 12/02/2016 |
Event Type
malfunction
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Manufacturer Narrative
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Zoll medical corporation has received the product and will be providing a follow-up report when our investigation is completed.
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Event Description
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Complainant alleged that while attempting to defibrillate a patient (age & gender unknown) the device was unable to sync.Complainant did not indicate that there was any adverse effect to the patient due to the reported malfunction.
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Manufacturer Narrative
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Zoll medical corporation evaluated the device and the reported malfunction was not replicated or confirmed.The device was put through extensive testing without duplicating the malfunction.The clinical data was not available for evaluation as part of this investigation.The device was returned to the customer untested since evaluation and service fees were declined by the customer.No trend is associated with reports of this type.
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Search Alerts/Recalls
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