FDA Adverse Event Malfunction Summary report: N

CPM

MDR report key: 1070723 · Received June 20, 2008

Report

Report Number
1070723
Event Type
Malfunction
Date Received
June 20, 2008
Date of Event
June 17, 2008
Report Date
June 20, 2008
Manufacturer
CHATTANOOGA GROUP
Product Code
BXB
Product Problem
Yes
Report Source
User Facility report
Reporter Location
TN, US

Narratives

Description of Event or Problem · 1

CPM MACHINE FROZE IN THE 90 DEGREE FLEXION. NURSES UNABLE TO CORRECT PROBLEM SO PATIENT'S KNEE REMOVED FOR THE REST OF THE NIGHT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CPM CONTINUOUS PASSIVE MOTION BXB CHATTANOOGA GROUP 04165064 *

Patients

Seq Age Sex Outcome Treatment
1 63 YR NO OTHER THERAPIES| NO OTHER THERAPIES