Model Number 866199 |
Device Problems
Insufficient Information (3190); Appropriate Term/Code Not Available (3191)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 10/27/2023 |
Event Type
malfunction
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Manufacturer Narrative
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A follow up report will be submitted upon completion of the investigation.
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Event Description
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It was reported to philips that the customer wants to order 4 batteries.Patient involvement information is currently unknown, but no reported adverse event.The efficia dfm100 defibrillator, model# 866199, is substantially similar to the heartstart xl+ defibrillator (model # 861290) and will be reported in the united states under device model # 861290.
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Event Description
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This report is based on information provided by philips field service personnel and has been investigated by the philips complaint handling team.Philips received a complaint on the efficia dfm100 defibrillator monitor indicating request order 4 batteries.The material order was canceled because the batteries has been backordered.Based on the information available and results of additional analysis, no further action is necessary at this time.Based on the review of the latest provided information, the reported allegation is currently being classified as a non-complaint.
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Manufacturer Narrative
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H3 other text : the material order was canceled because the batteries has been backordered.
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Search Alerts/Recalls
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