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Recall Observatory FDA recall evidence

Device product

Trilogy EVO Ventilator, 02 - Italy - Model Number: IT2100X21B Trilogy Evo is intended for pediatric through adult patients weighing at least 2.5 kg. The ventilator can measure, display, record, and alarm SpO2, FiO2, CO2, and Pulse Rate data when integrated with the appropriate accessories.

Z-0951-2020

November 19, 2019

Class I

Product summary

Firm
Philips Respironics, Inc.
Event
Event 84406
Status
Terminated
Classification
Class I
Quantity
3
Official record key
device-enforcement:Z-0951-2020

Official wording

Reason: Software defect in the Trilogy EVO and Trilogy EVO Universal Ventilator, versions SW 1.00.05, SW 1.01.09.00, SW 1.01.10.00, and SW 1.01.11.00, causing inoperative and loss of all power alarms. This defect causes an incorrect or unexpected result failing requirements TSRS1298 and PRD439.

Code information: Model/Material Number: IT2100X21B Serial Numbers: H24371481043C, H243714900C6D, H24371504C78D,

Distribution pattern: US: None OUS: CH DE DK IT FR IE GB KW QA PL ES AT PH AE SI CZ

Derived failure modes

  • Device software or design

    reason.device_software_design · v1.0.0

    Software defect