Model Number R SERIES |
Device Problems
Pacing Problem (1439); Defibrillation/Stimulation Problem (1573)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Type
malfunction
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Event Description
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Complainant alleged that while attempting to treat a patient (age & gender unknown), the device displayed "pacer disabled" and "defib disabled" messages.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 has received the product and will be providing a supplemental report when our investigation is completed.
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Manufacturer Narrative
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The device was evaluated by zoll medical corporation.The customer's report was duplicated and attributed to open fuse on the analog board.The analog board was replaced to resolve the report.The device was recertified and returned to the customer.Analysis of the report of this type has not identified an increase in trend.
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Search Alerts/Recalls
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