Model Number MMT-1715KM |
Device Problem
Appropriate Term/Code Not Available (3191)
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Patient Problem
Cardiac Arrest (1762)
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Event Date 09/11/2017 |
Event Type
Death
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Manufacturer Narrative
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(b)(4).Currently it is unknown whether or not the device may have caused or contributed to the event as no product has been returned.No conclusion can be drawn at this time.We therefore consider this report complete to the best of our knowledge.
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Event Description
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Medtronic legal received information regarding customer¿s passing on (b)(6) 2017 from the attorney of the family.The information received on october 20, 2021 stated the following : customer had died due to cardiac arrest as they were getting too much of insulin or no insulin and had type 1 diabetes.The insulin pump will not be returned for the analysis.
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Event Description
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Medtronic was notified on october 19, 2021.Attorney also alleged membrane vent block issue and retainer ring issue leading to customer's passing.Please see (b)(4) for the same case with more information on the customer's passing.
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Manufacturer Narrative
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The information has been updated and provided in this report.
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Search Alerts/Recalls
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