FDA Adverse Event Malfunction Summary report: N

COBE CENTRYSTEM 3

MDR report key: 56544 · Received December 17, 1996

Report

Report Number
1713683-1996-00277
Event Type
Malfunction
Date Received
December 17, 1996
Report Date
December 17, 1996
Manufacturer
GAMBRO HEALTHCARE
Product Code
FII
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

THE LIP THAT HOLDS THE CAM IS EITHER WORN AND/OR BROKE OFF AND THE CAMS ARE FALLING OUT OR NOT OCCLUDING THE TUBING SET, THERE WERE NO PT INJURIES OR MEDICAL INTERVENTIONS REPORTED. THE RETURNED FOUR-POSITION LINE CLAMP WAS VISUALLY INSPECTED AND CONFIRMED THAT THE CLAMP HOLDER WAS BROKEN. THE TABS ON THE WHITE CLAMP INSERT HOLDER WAS BROKEN OR STRETCHED, ALLOWING THE INSERTS TO FALL OUT OF THE HOLDER, IT WAS ALSO DETERMINED THAT THE RETURNED CLAMP STOP TABS WHICH HOLD THE CLAMP IN THE OCCLUDED POSITION WERE EITHER WORN OR BROKEN, SO THAT THE CLAMP NO LONGER STOPPED SECURELY IN THE CLOSED POSITION. THIS CONDITION OCCURRED WITH NORMAL USE. THE ABOVE INFO INDICATES THAT THE LINE CLAMP FAILURE DESCRIBED IN THIS COMPLAINT WAS GENERATED BY A BROKEN CLAMP ASSEMBLY. THIS ISSUE WILL CONTINUE TO BE TRENDED AS PART OF THE GAMBRO HEALTHCARE CORRECTIVE ACTION SYS AND THE MANAGEMENT REVIEW TEAM. ANY FURTHER INVESTIGATIONS, ANALYSES, AND/OR CORRECTIVE ACTIONS TAKEN ON THIS COMPLAINT ISSUE WILL BE DETERMINED BY AND DOCUMENTED IN THIS CORRECTIVE ACTION REVIEW PROCESS. SEE. FAR # 960027. CUSTOMER CONTACTED: NO SALES/SERVICE CONTACTED BY INVESTIGATOR? NO. TRAINING REQUIRED? NO.

Description of Event or Problem · 1

DURING A DIALYSIS TREATMENT, A 4 POSITION LINE CLAMP BROKE. THERE WAS NO PT INJURY OR MEDICAL INTERVENTION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 COBE CENTRYSTEM 3 DIALYSIS CONTROL UNIT FII GAMBRO HEALTHCARE NA NA

Patients

Seq Age Sex Outcome Treatment
1 UNKNOWN Other