FDA Adverse Event Malfunction Summary report: N

RETRO LONG-TERM HEMODIALYSIS CATHETER 16F FULL PROCEDURE T

MDR report key: 3802384 · Received February 21, 2014

Report

Report Number
3006260740-2014-00069
Event Type
Malfunction
Date Received
February 21, 2014
Date of Event
January 1, 2014
Report Date
January 30, 2014
Manufacturer
C.R. BARD, INC. (BASD)
Product Code
MSD
PMA / PMN Number
K022644
Product Problem
Yes
Report Source
Manufacturer report
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

UNABLE TO DETERMINE FROM PHOTO SAMPLE WHERE CRACK OCCURRED. THIS EVENT WILL BE CONSERVATIVELY REPORTED AS EXTERNAL BREAK OF DEVICE. THE COMPLAINT OF A BREAK IN THE VENOUS EXTENSION TUBING IS INCONCLUSIVE. THE IMAGES IN THE PHOTOS SHOW A BLUE VENOUS CAP COLLAR THAT IS LOOSE. A SUTURE HUB COLLAR CONNECTER THAT IS ATTACHED TO A SECTION OF CLEAR EXTENSION TUBING. THE COMPRESSION CLAMP IS ENGAGED AND IS LOCKED ONTO THE EXTENSION TUBING. A SMALL SEGMENT OF WHITE CATHETER TUBING IS LOOSELY PLACED ONTO METAL CANNULA OF THE SUTURE CONNECTOR. THE GRAY CONNECTOR HAS SEPARATED FROM THE CLEAR EXTENSION TUBING. A SEGMENT OF THE TUBING FIXED ON THE ARBS OF THE CONNECTOR. EVIDENCE OF A RED RESIDUAL MATERIAL IS SEEN THROUGHOUT THE COMPLAINT SAMPLE. NO OBVIOUS DAMAGE TO THE EXTENSION TUBING CAN BE DISCERNED FROM THE PHOTO. IF THE COMPLAINT SAMPLE IS RETURNED REGARDING THIS INCIDENT, THE INVESTIGATION WILL BE READDRESSED. A LOT HISTORY REVIEW (LHR) OF ASW0001 SHOWED ONE OTHER SIMILAR PRODUCT COMPLAINT(S) FROM THIS LOT NUMBER. BOTH COMPLAINTS FOR THIS LOT NUMBER (ASWC0001) HAVE BEEN REPORTED FROM ONE (B)(6) FACILITY.

Description of Event or Problem · 1

THE EXTENSION ON THE BLUE CONNECTOR WAS CRACKED DURING TREATMENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
110005 RETRO LONG-TERM HEMODIALYSIS CATHETER 16F FULL PROCEDURE T CATHETER, HEMODIALYSIS, IMPLANTED MSD C.R. BARD, INC. (BASD) ASWC0001

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention UNK.