Model Number 865350 |
Device Problem
Fire (1245)
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Patient Problem
No Known Impact Or Consequence To Patient (2692)
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Event Type
malfunction
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Manufacturer Narrative
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A follow up report will be submitted once the investigation is complete.
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Event Description
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The customer reported the patient stated the device leads caught fire.The customer indicated,.Oxygen & patient lighter was likely cause, not device, needs verification.Currently awaiting a response.
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Event Description
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The customer reported the patient stated the device leads caught fire.The customer indicated, oxygen & patient lighter was likely cause, not device, needs verification.The device was reported to be in use on a patient, but no adverse event to patient or user was reported.
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Manufacturer Narrative
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Submission of a report does not constitute an admission that medical personnel, user facility, importer, distributor, manufacturer, or product caused or contributed to the event.
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Search Alerts/Recalls
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