Device Problem
Insufficient Information (3190)
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Patient Problems
Cardiac Arrest (1762); Death (1802)
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Event Date 03/07/2013 |
Event Type
Death
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Manufacturer Narrative
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(b)(4).A supplemental report will be submitted upon completion of the plant's investigation.Additional information has been requested and will be submitted upon receipt accordingly.This is one of two device reports that are associated with this event.
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Event Description
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The plaintiff's attorney alleged that the patient experienced a cardiac arrest after receiving dialysis treatment and expired, which is alleged to have resulted from the product administered to the patient.
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Manufacturer Narrative
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Further attempts to obtain complete complaint details and upon receipt will be submitted accordingly.This is one of two device reports associated with this event.Related manufacturer report numbers are 1225714-2016-00075 and 1225714-2016-00076.
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Search Alerts/Recalls
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