← DeviceEvents
HomeDevice Adverse Events

CAPTURED SCREWDRIVER SHORT Adverse Event — Malfunction (MDR 0001822565-2020-01370)

CAPTURED SCREWDRIVER SHORT Adverse Event — Malfunction (MDR 0001822565-2020-01370) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: CAPTURED SCREWDRIVER SHORT; Generic name: TRAUMA INSTRUMENTATION; Manufacturer: ZIMMER BIOMET, INC..

DeviceCAPTURED SCREWDRIVER SHORT
Generic nameTRAUMA INSTRUMENTATION
ManufacturerZIMMER BIOMET, INC.
Report number0001822565-2020-01370
Event typeMalfunction
Product problemY
Date received2020-04-27
Report sourceDISTRIBUTOR, FOREIGN, HEALTH PR
NarrativeNO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
SourceopenFDA MAUDE (device adverse events)

🔍 Search all device adverse events →