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Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problem
Reaction (2414)
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Event Type
Injury
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Manufacturer Narrative
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The device was not returned and the lot number is unknown; therefore, a device analysis could not be completed.Should additional relevant information become available, a supplemental report will be submitted.
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Event Description
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It was reported that a folfusor device containing fluorouracil (no further details) was terminated nine hours in advance.The cause for the event was not reported.It was reported the patient experienced an unknown reaction.No further detail was provided regarding treatment or interventions for the event, if hospitalization was required or the patient¿s outcome.No additional information is available.
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Search Alerts/Recalls
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