FDA Adverse Event Malfunction Summary report: N

DEVILBISS

MDR report key: 14363363 · Received May 11, 2022

Report

Report Number
2515872-2022-00043
Event Type
Malfunction
Date Received
May 11, 2022
Report Date
May 26, 2022
Manufacturer
DEVILBISS HEALTHCARE LLC
Product Code
CAW
UDI-DI
00885304000846
PMA / PMN Number
K071397
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
OTHER
Health Professional
N

Narratives

Description of Event or Problem · 0

DURING A RETROSPECTIVE COMPLAINT REVIEW, DEVILBISS HEALTHCARE IDENTIFIED A DEVILBISS MODEL 525DS OXYGEN CONCENTRATOR WITH A COMPLAINT OF "UNIT WAS ALARMING AFTER RUNNING FOR 30 MINUTES AND HAS BURNING SMELL." THE COMPLAINT WAS REPORTED IN MAY OF 2018. THERE WAS NO REPORT OR EVIDENCE OF ILLNESS, INJURY OR MEDICAL TREATMENT ASSOCIATED WITH THE COMPLAINT. THE ROOT CAUSE INVESTIGATION REVEALED THERMAL DEFORMATION TO THE REAR CABINET AND COMPRESSOR HOUSING CAUSED BY A BENT FAN GUARD THAT PREVENTED THE COOLING FAN FROM SPINNING PROPERLY. DEVILBISS HAS AN ACTIVE CAPA FOR FAN RELATED ISSUES.

Description of Event or Problem · 0

DURING A RETROSPECTIVE COMPLAINT REVIEW, DEVILBISS HEALTHCARE EXAMINED A COMPLAINT RECEIVED FROM A DISTRIBUTOR IN MAY, 2018 INVOLVING A DEVILBISS OXYGEN CONCENTRATOR THAT "WAS ALARMING AFTER RUNNING FOR 30 MINUTES AND HAS BURNING SMELL." THERE WAS NO REPORT OR EVIDENCE OF ILLNESS, INJURY OR MEDICAL TREATMENT ASSOCIATED WITH THE COMPLAINT. DEVILBISS EVALUATED THE UNIT AT THE TIME AND DETERMINED THAT A BENT FAN GUARD PREVENTED THE COOLING FAN FROM SPINNING PROPERLY, RESULTING IN THERMAL DEFORMATION TO THE CABINET AND COMPRESSOR HOUSING. DEVILBISS HAS AN ACTIVE CAPA FOR FAN COMPLAINTS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1998826 DEVILBISS OXYGEN CONCENTRATOR CAW DEVILBISS HEALTHCARE LLC 525DS 00885304000846

Patients

Seq Age Sex Outcome Treatment
1 Unknown