Device Problem
Insufficient Information (3190)
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Patient Problems
Death (1802); Respiratory Failure (2484)
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Event Date 04/06/2006 |
Event Type
Death
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Manufacturer Narrative
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(b)(4).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 respiratory arrest following dialysis treatment 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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Additional information has been requested and will be submitted upon receipt accordingly.This is one of two device reports associated with this event.Related manufacturer report numbers are 1225714-2016-00054 and 1225714-2016-00055.
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Search Alerts/Recalls
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