FDA Adverse Event Injury Summary report: N

LUNA G3 BPAP 25A

MDR report key: 23265020 · Received October 10, 2025

Report

Report Number
3009096682-2025-00009
Event Type
Injury
Date Received
October 10, 2025
Date of Event
April 1, 2025
Report Date
September 16, 2025
Manufacturer
BMC MEDICAL CO., LTD
Product Code
BZD
Adverse Event
Yes
Report Source
Distributor report
Reporter Location
NY, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 0

IT WAS REPORTED TO 3B MEDICAL, INC. DBA REACT HEALTH THAT A PATIENT ALLEGEDLY DEVELOPED A BURN ON THE BRIDGE OF HIS NOSE APPROXIMATELY FOUR MONTHS AGO ((B)(6) 2025), WHICH SUBSEQUENTLY LEFT A SCAR. THE PATIENT ADVISED THAT HE WAS USING A RESMED AIRTOUCH N20 MASK, NOT A REACT HEALTH MASK. THE DEVICE HAS NOT BEEN RETURNED TO EITHER REACT HEALTH OR THE MANUFACTURER FOR AN EVALUATION. REACT HEALTH REACHED OUT TO THE PATIENT TO OBTAIN ADDITIONAL INFORMATION, AND HIS RESPONSES HAVE BEEN DOCUMENTED IN SECTION A. NO FURTHER DETAILS ABOUT THE PATIENT OR THE EVENT WERE PROVIDED. PAGE 20 OF THE LUNA G3 BPAP 25A USER MANUAL ADVISES THE FOLLOWING: ¿WARNINGS! - USE ONLY TUBING AND MASK PROVIDED BY REACT HEALTH.¿ [PLEASE NOTE: THE EVENT WAS REPORTED DIRECTLY TO REACT HEALTH BY THE PATIENT. AS A RESULT, SECTION E1 FIRST AND LAST NAME, AS WELL AS ADDRESS 1, SHALL BE LEFT BLANK AS IT IS PROTECTED HEALTH INFORMATION (PHI)].

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
312030 LUNA G3 BPAP 25A VENTILATOR, NON-CONTINUOUS (RESPIRATOR) BZD BMC MEDICAL CO., LTD G3-B25A N/A

Patients

Seq Age Sex Outcome Treatment
1 NA Male RESMED AIRTOUCH N20 NASAL CPAP MASK.