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EDGE Adverse Event — Malfunction (MDR 10000449)

EDGE Adverse Event — Malfunction (MDR 10000449) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: EDGE; Generic name: ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES; Manufacturer: COVIDIEN.

DeviceEDGE
Generic nameELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES
ManufacturerCOVIDIEN
Report number10000449
Event typeMalfunction
Product problemY
Date received2020-04-27
NarrativeBRONCHOSCOPE ADAPTER WOULD NOT PASS THROUGH PORT HOLE. ANOTHER WAS OBTAINED AND IT WORKED. THERE WAS NO HARM TO PATIENT. ADAPTER NUMBER: SD303BA.
SourceopenFDA MAUDE (device adverse events)

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