FDA Adverse Event Injury Summary report: N

MARK II, URIXSON, HIP POSITIONER

MDR report key: 58898 · Received December 26, 1996

Report

Report Number
58898
Event Type
Injury
Date Received
December 26, 1996
Date of Event
May 16, 1996
Report Date
July 11, 1996
Manufacturer
INNOMED, INC.
Product Code
KIL
Adverse Event
Yes
Report Source
User Facility report
Reporter Location
CO, US
Reporter Occupation
RISK MANAGER

Narratives

Description of Event or Problem · 1

WHEN REMOVING THE HIP POSITIONER AFTER THE CASE IT WS NOTED THAT THE POSTERIOR POST WAS BENT AND WAS PROTRUDING INTO THE PT R BUTTOCK. TISSUE WAS REDDENED WITH WHITE INDENTATION BUT NO BREAKDOWN NOTED AT THAT TIME. AREA WAS 4" X 4".

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 MARK II, URIXSON, HIP POSITIONER HIP POSITIONER KIL INNOMED, INC. * *

Patients

Seq Age Sex Outcome Treatment
1 72 YR