YELLOFINS STIRRUP Adverse Event — Malfunction (MDR 10000438)

Name: YELLOFINS STIRRUP Adverse Event — Malfunction (MDR 10000438)
Creator: DeviceEvents

YELLOFINS STIRRUP Adverse Event — Malfunction (MDR 10000438) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: YELLOFINS STIRRUP; Generic name: SUPPORT, PATIENT POSITION; Manufacturer: ALLEN MEDICAL SYSTEMS, INC..

Device	YELLOFINS STIRRUP
Generic name	SUPPORT, PATIENT POSITION
Manufacturer	ALLEN MEDICAL SYSTEMS, INC.
Report number	10000438
Event type	Malfunction
Product problem	Y
Date received	2020-04-27
Narrative	RIGHT LEG STIRRUP CAME OUT OF BRACKET WITH PATIENT'S LEG IN THE STIRRUP. THE STIRRUP CAME OUT OF THE STIRRUP HOLDER DURING SURGERY. SURGEON WAS STANDING NEXT TO LEG AND WAS ABLE TO HOLD LEG AND IT WAS AT THE END OF THE CASE. NO HARM TO THE PATIENT. BIOMED TECH TESTED YELLOFINS STIRRUPS. CONNECTED BOTH BRACKETS TO SURGERY BED. BRACKETS TIGHT AND STIRRUP WAS MOVED TO DIFFERENT DIRECTIONS. UNIT WAS S
Source	openFDA MAUDE (device adverse events)

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