Model Number X SERIES |
Device Problem
Pacing Problem (1439)
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Patient Problem
No Consequences Or Impact To Patient (2199)
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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 pace a patient (age & gender unknown), the device was unable to pace.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.Please reference medwatch report 1220908-2018-02941 for a similar event reported from the same customer.
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Manufacturer Narrative
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The reported malfunction was observed during testing.However during trouble-shooting it could not be verified to a component or assembly.Upon reassembly the report could no longer be duplicated.The left side panel was replaced as precaution.The device was recertified and returned to the customer.Analysis of reports of this type has not identified an increase in trend.
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Search Alerts/Recalls
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