Device Problem
Insufficient Information (3190)
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Patient Problems
Cardiopulmonary Arrest (1765); Death (1802)
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Event Date 02/21/2013 |
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, approximately six days after receiving dialysis treatment, the patient experienced a fatal cardiopulmonary arrest and subsequently expired, which is alleged to have been caused by the product administered to the patient for dialysis treatment.
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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 1225714-2016-00079 and 1225714-2016-00080.
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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 1225714-2016-00079 and 1225714-2016-00080.
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Event Description
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The plaintiff's attorney alleged the patient experienced a fatal cardiopulmonary arrest and subsequently expired 6 days later, which is alleged to have been caused by the product administered to the patient for dialysis treatment.
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Search Alerts/Recalls
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