FDA Adverse Event Malfunction Summary report: N

CATHETER MOUNT

MDR report key: 4052080 · Received September 2, 2014

Report

Report Number
9611451-2014-00743
Event Type
Malfunction
Date Received
September 2, 2014
Report Date
August 7, 2014
Manufacturer
FISHER & PAYKEL HEALTHCARE LTD
Product Code
BZO
PMA / PMN Number
SEE H10
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
AS
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). THE RT021 IS SOLD IN THE USA BUT HAS NO 510(K) NUMBER AS IT IS CONSIDERED A CLASS I DEVICE. METHOD: TWO COMPLAINT RT021 CATHETER MOUNTS WERE RETURNED TO FISHER & PAYKEL HEALTHCARE IN (B)(4) AND WERE VISUALLY INSPECTED. RESULTS: VISUAL INSPECTION REVEALED THAT THE TUBING CUFF OF BOTH CATHETER MOUNTS WAS SPLIT AT THE SWIVEL END. A LOT CHECK REVEALED NO OTHER COMPLAINTS OF THIS NATURE FOR LOT NUMBER 140306. CONCLUSION: WE ARE UNABLE TO DETERMINE THE CAUSE OF THE DAMAGE TO THE RETURNED RT021 DEVICES. ALL RT021 CATHETER MOUNTS ARE PRESSURE TESTED AND VISUALLY INSPECTED PRIOR TO BEING RELEASED FOR DISTRIBUTION. ANY CATHETER MOUNT WITH A SPLIT TUBE OR A DETACHED SEAL WOULD HAVE FAILED THE PRESSURE TEST. THIS SUGGESTS THAT THE RETURNED CATHETER MOUNTS BECAME DAMAGED AFTER THEY WERE RELEASED FOR DISTRIBUTION. OUR USER INSTRUCTIONS THAT ACCOMPANY THE RT021 CATHETER MOUNT STATE THE FOLLOWING: - CHECK ALL CONNECTIONS ARE TIGHT BEFORE USE - PERFORM A PRESSURE AND LEAK TEST ON THE BREATHING SYSTEM AND CHECK FOR OCCLUSIONS BEFORE CONNECTING TO A PATIENT

Description of Event or Problem · 1

A HOSPITAL IN (B)(6) REPORTED VIA A FISHER & PAYKEL HEALTHCARE FIELD REPRESENTATIVE THAT TWO RT021 CATHETER MOUNTS WERE LEAKING. NO PATIENT CONSEQUENCE REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
534012 CATHETER MOUNT BZO BZO FISHER & PAYKEL HEALTHCARE LTD RT021 140306

Patients

Seq Age Sex Outcome Treatment
1