FDA Adverse Event Malfunction Summary report: N

DREAMSTATION BIPAP ST

MDR report key: 18273387 · Received December 6, 2023

Report

Report Number
2518422-2023-33361
Event Type
Malfunction
Date Received
December 6, 2023
Date of Event
November 22, 2023
Manufacturer
RESPIRONICS, INC.
Product Code
MNS
UDI-DI
00606959045606
PMA / PMN Number
K102465
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
003

Narratives

Additional Manufacturer Narrative · 0

THE MANUFACTURER RECEIVED INFORMATION IN RELATION TO A DREAMSTATION BIPAP ST30 H/HT/C, DS UNIT. THE DEVICE WAS RETURNED TO A THIRD PARTY SERVICE CENTER. DURING VISUAL INSPECTION OF THE DEVICE, IT WAS DETERMINED THE POWER CONNECTOR OF THE UNIT WAS CORRODED. DEVICE WAS SCRAPPED AT CUSTOMER'S REQUEST. ANALYSIS OF PAST EVENTS HAS NOT INDICATED AN ADVERSE EVENT HAS OCCURRED DUE TO CORROSION. REVIEW OF THE RISK FILE INDICATES THE POTENTIAL FOR A SERIOUS ADVERSE EVENT OCCURRING AS A RESULT OF THIS INCIDENT IS UNLIKELY. ADDITIONALLY, THE RISK FILE INDICATES THAT CORROSION WILL NOT SUBSTANTIALLY AFFECT THE PERFORMANCE OF THE DEVICE. THIS COMPLAINT IS CONSIDERED NOT REPORTABLE.

Additional Manufacturer Narrative · 0

H3 OTHER TEXT : DEVICE NOT RETURNED TO MANUFACTURER.

Description of Event or Problem · 0

THE MANUFACTURER RECEIVED INFORMATION REGARDING A DREAMSTATION BIPAP ST. THE DEVICE WAS RETURNED TO A THIRD PARTY SERVICE CENTER. DURING VISUAL INSPECTION OF THE DEVICE, CORROSION WAS FOUND IN DEVICE. THIS REPORT IS BEING SUBMITTED FOR THE CORROSION WAS FOUND IN DEVICE DURING SERVICE. NO EVIDENCE OF FOAM PARTICLES WAS OBSERVED WITHIN THE DEVICE. THERE WAS NO ALLEGATION OF SERIOUS OR PERMANENT HARM OR INJURY. THE DEVICE WAS SCRAPPED. NO MEDICAL INTERVENTION WAS REQUIRED FOR THE PATIENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
732195 DREAMSTATION BIPAP ST VENTILATOR, CONTINUOUS, NON-LIFE-SUPPORTING MNS RESPIRONICS, INC. DSX1030T11C 00606959045606

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown