FDA Adverse Event Malfunction Summary report: N

2082643-1999-01218

MDR report key: 256967 · Received December 23, 1999

Report

Report Number
2082643-1999-01218
Event Type
Malfunction
Date Received
December 23, 1999
Date of Event
November 30, 1999
Report Date
December 22, 1999
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
AZ, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

RPTR CLAIMS X-TUBE BROKE AT BOLT HOLE WHILE CHAIR WAS IN USE. NO INJURIES INVOLVED.

Patients

Seq Age Sex Outcome Treatment
1 43 YR Other