FDA Adverse Event Malfunction Summary report: N

FULL FACE MASK

MDR report key: 1031411 · Received April 18, 2008

Report

Report Number
9611451-2008-00145
Event Type
Malfunction
Date Received
April 18, 2008
Date of Event
February 19, 2008
Report Date
February 19, 2008
Manufacturer
FISHER & PAYKEL HEALTHCARE, LTD.
Product Code
MNT
PMA / PMN Number
K060044
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE RETURNED DEVICES WERE INSPECTED. RESULTS - THE SILICONE SEAL HAD SEPARATED FROM THE MASK BASE. NO OTHER ANOMALIES WERE IDENTIFIED IN THE DEVICE. THE IMPROPER FITTING OF THE MASK MAY HAVE CONTRIBUTED TO THE SILICONE SEAL SEPARATING FROM THE BASE OF THE MASK. THE RT040 MASK IS RELATIVELY NEW TO THE MARKET AND MANY USERS HAVE BEEN CONVERTING FROM A PREVIOUSLY USED COMPETITOR'S DEVICE TO THE RT040 AND AS A RESULT MAY NOT BE PROFICIENT WITH THE SIZING AND FITTING OF THE RT040. CONCLUSIONS - FISHER & PAYKEL HEALTHCARE HAS IMPLEMENTED AN IN-SERVICE EDUCATION PROGRAM TO FURTHER ENSURE THAT HEALTHCARE PRACTITIONERS FULLY UNDERSTAND THE PROPER FITTING OF THE RT040 MASK. THIS PROGRAM HAS BEEN AND CONTINUES TO BE ROLLED OUT TO CUSTOMERS IN THE UNITED STATES. IN ADDITION, WE HAVE INTRODUCED AN ADDITIONAL SILICONE ADHESIVE STEP (TO APPLY ADHESIVE BETWEEN THE SILICONE FACIAL SEAL AND THE PLASTIC MASK BASE) IN OUR MFG PROCESS WHICH IS AIMED AT REDUCING THE POTENTIAL FOR SEPARATION TO OCCUR. WE HAVE RECEIVED SIMILAR COMPLAINTS AND ARE CURRENTLY TRENDING THIS AT AN OCCURRENCE RATE OF APPROX 0.0531% WORLDWIDE FOR THE PAST YEAR.

Description of Event or Problem · 1

A HEALTHCARE FACILITY REPORTED TO OUR DISTRIBUTOR THAT TWO RT040M FULL FACE MASKS CAME APART WHILE BEING USED ON A PT. NO PT CONSEQUENCES WERE REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 FULL FACE MASK MNT FISHER & PAYKEL HEALTHCARE, LTD. RT040M 071203

Patients

Seq Age Sex Outcome Treatment
1