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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: RESPIRONICS, INC. TRILOGY EV300; VENTILATOR, CONTINUOUS, FACILITY USE

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RESPIRONICS, INC. TRILOGY EV300; VENTILATOR, CONTINUOUS, FACILITY USE Back to Search Results
Model Number FX2200X15B
Medical Device Problem Code Output Problem (3005)
Health Effect - Clinical Code No Clinical Signs, Symptoms or Conditions (4582)
Date of Event 03/04/2025
Type of Reportable Event Malfunction
Event or Problem Description
The manufacturer received information alleging pip and pressure graph not coming.There was no harm or injury reported.Material only workorder created for shipment of replacement system board.
 
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Brand Name
TRILOGY EV300
Common Device Name
VENTILATOR, CONTINUOUS, FACILITY USE
Manufacturer (Section D)
RESPIRONICS, INC.
1001 murry ridge lane
murrysville PA
Manufacturer (Section G)
RESPIRONICS, INC.
1001 murry ridge lane
murrysville PA
Manufacturer Contact
melissa rosko
6501 living place
pittsburgh, PA 
4125423300
MDR Report Key21752785
Report Number2518422-2025-103619
Device Sequence Number8220229
Product Code CBK
UDI-Device Identifier00606959061033
UDI-Public(01)00606959061033
Combination Product (Y/N)N
Initial Reporter CountryIN
PMA/510(K) Number
K181166
Number of Events Summarized1
Summary Report (Y/N)N
Serviced by Third Party (Y/N)N
Reporter Type Manufacturer
Report Source Foreign,Company Representative
Initial Reporter Occupation Other
Type of Report Initial
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Model NumberFX2200X15B
Device Catalogue NumberFX2200X15B
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer 03/04/2025
Initial Report FDA Received Date04/02/2025
Was Device Evaluated by Manufacturer? (Y/N) No
Date Device Manufactured01/28/2021
Is the Device Labeled for Single Use? (Y/N) No
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)
No
Usage of Device Reuse
Patient Sequence Number1
Patient SexUnknown
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