FDA Adverse Event Malfunction Summary report: N

BROVIAK 2.7 FRENCH SINGLE LUMEN CATHETER

MDR report key: 8981 · Received August 11, 1993

Report

Report Number
8981
Event Type
Malfunction
Date Received
August 11, 1993
Date of Event
February 25, 1993
Report Date
June 25, 1993
Manufacturer
BARD ACCESS
Product Code
FEF
Product Problem
Yes
Report Source
User Facility report

Narratives

Description of Event or Problem · 1

THE CVC LINE DISCONNECTED AT Y-SITE. THE PATIENT HAD TO RETURN TO SURGERY FOR REPLACEMENT OF THE CVC LINE. THE FIRST LINE WAS PLACED ON FEBRUARY 19 AND THE SECOND LINE WAS PLACED ON FEBRUARY 25, 1993. THE PATIENT WAS READMITTED IN APRIL, 1993. AT THAT TIME THE SECOND WAS NOTED TO BE DOING THE SAME THING THE FIRST LINE DID. THE LINE WAS BUBBLING UP CAUSING THE CVC LINE TO CLOT OFF. DURING THIS MAY INPATIENT VISIT, THE STAFF THOUGHT THAT THE LINE MIGHT BE DEFECTIVE.DEVICE LABELED FOR SINGLE USE. PATIENT MEDICAL STATUS PRIOR TO EVENT: SATISFACTORY CONDITION. THERE WAS NOT MULTIPLE PATIENT INVOLVEMENT.INVALID DATA - ON DEVICE SERVICE/MAINTENANCE. NO DATA - REGARDING DATE LAST SERVICED. SERVICE PROVIDED BY: INVALID DATA. INVALID DATA - SERVICE RECORDS AVAILABILITY.NO IMMINENT HAZARD TO PUBLIC HEALTH CLAIMED. DEVICE USED AS LABELED/INTENDED.INVALID DATA - REGARDING EVALUATION BY USER AFTER EVENT. METHOD OF EVALUATION: INVALID DATA, INVALID DATA. RESULTS OF EVALUATION: MANUFACTURING, INVALID DATA. CONCLUSION: DEVICE FAILURE DIRECTLY CAUSED EVENT. CERTAINTY OF DEVICE AS CAUSE OF OR CONTRIBUTOR TO EVENT: YES. CORRECTIVE ACTIONS: DEVICE DISCARDED. INVALID DATA - ON DEVICE DESTROYED/DISPOSED OF STATUS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 BROVIAK 2.7 FRENCH SINGLE LUMEN CATHETER FEF BARD ACCESS 36IC0676

Patients

Seq Age Sex Outcome Treatment
1 1 YR Other