FDA Adverse Event Malfunction Summary report: N

2082643-1999-01226

MDR report key: 257093 · Received December 29, 1999

Report

Report Number
2082643-1999-01226
Event Type
Malfunction
Date Received
December 29, 1999
Date of Event
December 6, 1999
Report Date
December 23, 1999
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NC, US
Reporter Occupation
SERVICE PERSONNEL

Narratives

Description of Event or Problem · 1

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

Patients

Seq Age Sex Outcome Treatment
1 41 YR Other