Model Number X SERIES |
Device Problem
Failure to Discharge (1169)
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Patient Problem
Ventricular Tachycardia (2132)
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Event Date 05/19/2018 |
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 supplemental report when our investigation is completed.
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Event Description
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Complainant alleged that while attempting to treat a male patient (age unknown), the device failed to discharge.Complainant indicated that the clinician obtained another device to continue treating the patient.Complainant indicated that there was no 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 troubleshooting without duplicating the malfunction.The device was recertified and returned to the customer.Review of the activity logs did not find evidence to support the customer report.No trend is associated with reports of this type.
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Search Alerts/Recalls
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