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FDA MAUDE Adverse Event Report
MAUDE Adverse Event Report: COVIDIEN CIRCULAR STAPLER WITH DST SERIES TECHNOLOGY (EEA STAPLER) SURGICAL STAPLER
Event Description: 
Device did not function properly and did not "fire" appropriately. Another device opened. Case proceeded. No patient injury .
Lot Number P4K0403KX 
Event Date 06/25/2015 
Event Type  Malfunction