FDA Adverse Event Other Summary report: N

5890 FIXED JACKSON TABLE BASE

MDR report key: 476010 · Received July 29, 2003

Report

Report Number
2921578-2003-00002
Event Type
Other
Date Received
July 29, 2003
Report Date
July 18, 2003
Manufacturer
ORTHOPEDIC SYSTEMS, INC.
Product Code
BWN
Report Source
Manufacturer report
Reporter Location
MO, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

PT PLACED IN A SUPINE POSITION ON THE FRACTURE TABLE, AND THEIR ARMS WERE BROUGHT ACROSS PT AND HELD IN PLACE BY A DRAW SHEET AND TWO SURGICAL CLIPS. THE PT'S LEFT FOOT WAS PLACED IN A LEG HOLDER, AND THEIR RIGHT FOOT WAS HAVING TRACTION APPLIED MANUALLY. A PHYSICIAN WAS IN ATTENDANCE ON THE PT'S RIGHT SIDE, A PELVIC HOLDER WAS IN PLACE BETWEEN PT'S LEGS FOR POSITIONING WHEN THE BOTTOM PIECE OF THE FRACTURE TABLE WAS REMOVED. WITH ELEVATION OF THE BED, THE PT WAS PULLED TO THE RIGHT SIDE, SLID AND SUBSEQUENTLY FELL AGAINST THE PT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 5890 FIXED JACKSON TABLE BASE OPERATING ROOM TABLE BWN ORTHOPEDIC SYSTEMS, INC. 5890 *

Patients

Seq Age Sex Outcome Treatment
1 25 YR 5927, RADIOLUCENT IMAGING TABLE (2002 (STOP'D)),| 5855, RADIOLUCENT ORTHOPEDIC TABLE (2002 (STOP'D))