Device Problem
Insufficient Information (3190)
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Patient Problems
Cardiac Arrest (1762); Death (1802)
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Event Date 09/10/2014 |
Event Type
Death
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Manufacturer Narrative
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(b)(4).This is one of two device reports related to this event.Additional information has been requested and will be submitted upon receipt accordingly.
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Event Description
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The plaintiff's attorney alleged the patient experienced a sudden cardiac event and expired the same day, which is alleged to have been caused by the product administered during dialysis treatment.
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Manufacturer Narrative
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This is one of two device reports related to this event.Associated manufacturer report numbers are 1225714-2016-00042 and 1225714-2016-00043.Additional information has been requested and will be submitted upon receipt accordingly.
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Search Alerts/Recalls
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