FDA Adverse Event Malfunction Summary report: N

TRAPEZE

MDR report key: 36685 · Received September 4, 1996

Report

Report Number
MW4001474
Event Type
Malfunction
Date Received
September 4, 1996
Date of Event
March 23, 1995
Report Date
July 25, 1995
Manufacturer
UNK
Product Code
ILZ
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
MA, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

RESIDENT REACHED UP TO USE TRAPEZE. TRAPEZE LET GO AND HIT RESIDENT ON RIGHT SIDE OF FOREHEAD.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TRAPEZE TRAPEZE ILZ UNK UNK UNK

Patients

Seq Age Sex Outcome Treatment
1 88 YR