FDA Adverse Event Malfunction Summary report: N

NON-HEATED ADULT BREATHING CIRCUIT

MDR report key: 2874757 · Received December 16, 2012

Report

Report Number
9611451-2012-00888
Event Type
Malfunction
Date Received
December 16, 2012
Date of Event
November 2, 2012
Report Date
November 13, 2012
Manufacturer
FISHER & PAYKEL HEALTHCARE LTD
Product Code
BZO
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
JA
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). METHOD: THE RETURNED COMPLAINT BREATHING CIRCUIT WAS PRESSURE TESTED AND SUBMERGED IN A WATER BATH TO TEST FOR LEAKS. RESULTS: A LEAK WAS FOUND IN THE INSPIRATORY AND EXPIRATORY WATER TRAP. THE WATER TRAP OF THE BREATHING CIRCUIT CONSISTS OF TWO PARTS WHERE THE LOWER PART CAN BE REMOVED DURING USE FOR DRAINING WATER. THE WATER TRAP LEAK WAS LOCATED AT THE SEAL BETWEEN THE WATER TRAP BOWL AND THE WATER TRAP LID. A LOT CHECK REVEALED NO OTHER COMPLAINTS FOR LOT NUMBER 110907. CONCLUSION: ALL CIRCUITS ARE PRESSURE TESTED FOR LEAKS DURING PRODUCTION AND THOSE THAT FAIL ARE REJECTED. THIS SUGGESTS ANY LEAK MUST HAVE DEVELOPED POST PRODUCTION DURING TRANSPORT, STORAGE OR USE, POSSIBLY BY DISTORTION OF THE WATER TRAP WHEN THE BOWL WAS CONNECTED. THE USER INSTRUCTIONS THAT ACCOMPANY THE RT134 ADULT BREATHING CIRCUIT STATE THE FOLLOWING: "PERFORM A PRESSURE AND LEAK TEST ON THE BREATHING SYSTEM AND CHECK FOR OCCLUSIONS BEFORE CONNECTING TO A PATIENT." "SET APPROPRIATE VENTILATOR ALARMS. (B)(4).

Description of Event or Problem · 1

A HOSPITAL IN (B)(6) REPORTED VIA OUR DISTRIBUTOR THAT AN RT134 ADULT BREATHING CIRCUIT FAILED THE SERVO VENTILATOR LEAK TEST. THIS WAS FOUND BEFORE USE ON A PATIENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 NON-HEATED ADULT BREATHING CIRCUIT BZO BZO FISHER & PAYKEL HEALTHCARE LTD RT134 090407

Patients

Seq Age Sex Outcome Treatment
1