--- title: "Trilogy Evo EV300 -- Model Number/ Model Description: BL2200X15B Trilogy Evo,... — FDA record Z-2942-2024 | Is It on Recall" description: "Firm has released a mandatory software update Version 1.05.10.00 and a User Manual addendum for affected ventilators. These updates resolve safety issues identi" url: https://isitonrecall.com/recall/fda-device-z-2942-2024-trilogy-evo-ev300-model-number-model-description-bl2200x15b-trilogy-evo-o2-benelux-ev300-br2200x18b/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement # Trilogy Evo EV300 -- Model Number/ Model Description: BL2200X15B Trilogy Evo, O2, Benelux EV300; BR2200X18B Trilogy E... — FDA record Z-2942-2024 Reported ongoing Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice. Source date Jul 16, 2024. Retrieved Oct 1, 2026. Last updated Oct 1, 2026. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## What the record says - **Product**: Trilogy Evo EV300 -- Model Number/ Model Description: BL2200X15B Trilogy Evo, O2, Benelux EV300; BR2200X18B Trilogy Evo, O2, Brazil EV300; CA2200X12B Trilogy Evo, O2, Canada EV300; DE2200X13B Trilogy Evo, O2, Germany EV300; DS2200X11B Trilogy Evo, O2, USA EV300; DS2200X11B Trilogy Evo, O2, USA EV300; EE2200X15B Trilogy Evo, O2, Eastern Europe EV300; ES2200X15B Trilogy Evo, O2, Spain EV300; EU2200X15B Trilogy Evo, O2, EU EV300; FR2200X14B Trilogy Evo, O2, France EV300; FX2200X15B Trilogy Evo, O2, INT EV300; GB2200X15B Trilogy Evo, O2, Great Britain EV300; IN2200X15B Trilogy Evo, O2, INTL EV300; IT2200X21B Trilogy Evo, O2, Italy EV300; KR2200X15B Trilogy Evo, O2, Korea EV300; ND2200X15B Trilogy Evo, O2, Nordics EV300; TR2200X15B Trilogy Evo, O2, Turkey EV300; - **Reason**: Firm has released a mandatory software update Version 1.05.10.00 and a User Manual addendum for affected ventilators. These updates resolve safety issues identified in earlier recalls. - **Classification**: Class I - **Recalling firm**: Philips Respironics, Inc. - **Quantity**: 90,910 US; 56,273 ROW - **Agency-reported status**: Ongoing - **Source record identifier**: Z-2942-2024 [Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2942-2024%22) [What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice. ## Lot and product identifiers | Label field | Details supplied by the agency | | --- | --- | | Lot, code or applicability | Model / UDI-DI: Trilogy Evo, O2, Benelux EV300 606959058668; Trilogy Evo, O2, Brazil EV300 606959058583; Trilogy Evo, O2, Canada EV300 606959052321; Trilogy Evo, O2, Germany EV300 606959058651; Trilogy Evo, O2, USA EV300 606959052017; Trilogy Evo, O2, USA EV300 606959052017; Trilogy Evo, O2, Eastern Europe EV300 606959058705; Trilogy Evo, O2, Spain EV300 606959058644; Trilogy Evo, O2, EU EV300 606959058682; Trilogy Evo, O2, France EV300 606959058613; Trilogy Evo, O2, INT EV300 606959061033; Trilogy Evo, O2, Great Britain EV300 606959058675; Trilogy Evo, O2, INTL EV300 606959056497; Trilogy Evo, O2, Italy EV300 606959058637; Trilogy Evo, O2, Korea EV300 606959058590; Trilogy Evo, O2, Nordics EV300 606959058620; Trilogy Evo, O2, Turkey EV300 606959058798; US Serial Numbers: H284098132DDA 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H291251872A16 H29125512C9C2 H29125520C0B8 H29125527B407 H2912556284CA H291255639543 H29125564E1FC H29125565F075 H29125566C2EE H29125567D367 H291255693A19 H29125570BE00 H29125571AF89 H291255729D12 H291255738C9B H29125574F824 H291255783248 H2912557923C1 H291255830F53 H291255856A65 H29125589A009 H29125593168B H291256023F7E H2912561005B4 H291256144390 H2912561889FC H291256220CCE H291256264AEA H291256303604 H29125633049F H29125639ABC5 H29125648F744 H29125651735D H291256673C03 H291256727276 H29125680D2AC H29125698473C H291257015739 H291257225612 H29125723479B H2912572522AD H2912572701BF H29125728F948 H29125729E8C1 H2912574644E6 H291257512981 H291257565D3E H29125759A5C9 H291257623172 H2912576545CD H2912576766DF H291257733923 H2912577887F0 H291257808870 H29125787FCCF H29125792B2BA H29125795C605 H291257990C69 H291258011DFE H291258212E4E H291262115291 H291262253EDD H291262271DCF H29126247491F H2912625135F1 H291263507EA4 H29126358F2EC H291263614545 H2912636277DE H291263636657 H2912636412E8 H291263650361 H291263672073 H29126369C90D H29126381DF55 H2912638488F8 H29126389531D H29126402AF0B H2912641095C1 H291264229CBB H291264393BB0 H29126451E328 H29126461C940 H29126473F38A H291264815350 H29126488CE91 H291264914A88 H29126498D749 H29126502F5D7 H29126507A27A H29126513FD86 H291265148939 H29126531ED24 H2912654292B7 H29126550A87D H291265709BCD H29126757697A H29126778A23D H291268103062 H291268289642 H29126837776D H291268527410 H291268634FF1 H2912687247A0 H29126879F973 H291269025074 H29126908FF2E H291269153D13 H2912692625E0 H291269401406 H29126948984E H2912696027B6 H291269774AD1 H291270628401 H29127141DFF6 H29127175B3BA H2912731552D2 H29127329B2D6 H291273374270 H29127343495C H29127359FFDE H29127390CBBF H29127412AA68 H29127425F4BF H291274338851 H29127440F7C2 H29127503F8E5 H29127516B690 H29127547D9A1 H291275910CEF H29127606402C H291276147AE6 H29127624508E H291276366A44 H291276514A2B H291276706812 H291276771CAD H291276868EEC H2912803359C9 H29128059A243 H2912806670DC H2912856758E8 H2912857650B9 H29128625F3FE H291286951756 H29128716B1D1 H29128756D6B1 H291287855452 H2912879987E6 H29128863E1B3 H291288795731 H2912893783F3 H29128954E5B8 H291289593E5D H291289911BB5 H291289966F0A H29129008D1C9 H2912901155D0 H291290260B07 H2912903431CD H2912903612DF ... | The agency lot list is longer than this excerpt. [Read the complete list at the official source](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2942-2024%22). Match all identifying details in the current notice. A brand name alone is not enough. ## Distribution Worldwide distribution: US (nationwide) and OUS (foreign) countries of: AU, BD, BE, BG, BO, BR, BS, CH, CL, NL, CN, CO, CZ, DE, DK, FR, SE, GB, GF, GR, GT, HK, HR, HU, IE, IL, IN, IT, JP, KE, KW, LB, LT, MA, ME, MA, MT, MQ, MX, NO, NP, OM, PA, PE, PF, PK, PL, PT, PY, QA, RE, RO, RS, RU, SA, SE, SI, SK, SG, TH, TN, TR, TW, UA, YT, ZA and ZW. States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address. - [Alaska](https://isitonrecall.com/state/alaska/) - [Alabama](https://isitonrecall.com/state/alabama/) - [Arkansas](https://isitonrecall.com/state/arkansas/) - [Arizona](https://isitonrecall.com/state/arizona/) - [California](https://isitonrecall.com/state/california/) - [Colorado](https://isitonrecall.com/state/colorado/) - [Connecticut](https://isitonrecall.com/state/connecticut/) - [Delaware](https://isitonrecall.com/state/delaware/) - [Florida](https://isitonrecall.com/state/florida/) - [Georgia](https://isitonrecall.com/state/georgia/) - [Hawaii](https://isitonrecall.com/state/hawaii/) - [Iowa](https://isitonrecall.com/state/iowa/) - [Idaho](https://isitonrecall.com/state/idaho/) - [Illinois](https://isitonrecall.com/state/illinois/) - [Indiana](https://isitonrecall.com/state/indiana/) - [Kansas](https://isitonrecall.com/state/kansas/) - [Kentucky](https://isitonrecall.com/state/kentucky/) - [Louisiana](https://isitonrecall.com/state/louisiana/) - [Massachusetts](https://isitonrecall.com/state/massachusetts/) - [Maryland](https://isitonrecall.com/state/maryland/) - [Maine](https://isitonrecall.com/state/maine/) - [Michigan](https://isitonrecall.com/state/michigan/) - [Minnesota](https://isitonrecall.com/state/minnesota/) - [Missouri](https://isitonrecall.com/state/missouri/) - [Mississippi](https://isitonrecall.com/state/mississippi/) - [Montana](https://isitonrecall.com/state/montana/) - [North Carolina](https://isitonrecall.com/state/north-carolina/) - [North Dakota](https://isitonrecall.com/state/north-dakota/) - [Nebraska](https://isitonrecall.com/state/nebraska/) - [New Hampshire](https://isitonrecall.com/state/new-hampshire/) - [New Jersey](https://isitonrecall.com/state/new-jersey/) - [New Mexico](https://isitonrecall.com/state/new-mexico/) - [Nevada](https://isitonrecall.com/state/nevada/) - [New York](https://isitonrecall.com/state/new-york/) - [Ohio](https://isitonrecall.com/state/ohio/) - [Oklahoma](https://isitonrecall.com/state/oklahoma/) - [Oregon](https://isitonrecall.com/state/oregon/) - [Pennsylvania](https://isitonrecall.com/state/pennsylvania/) - [Rhode Island](https://isitonrecall.com/state/rhode-island/) - [South Carolina](https://isitonrecall.com/state/south-carolina/) - [South Dakota](https://isitonrecall.com/state/south-dakota/) - [Tennessee](https://isitonrecall.com/state/tennessee/) - [Texas](https://isitonrecall.com/state/texas/) - [Utah](https://isitonrecall.com/state/utah/) - [Virginia](https://isitonrecall.com/state/virginia/) - [Vermont](https://isitonrecall.com/state/vermont/) - [Washington](https://isitonrecall.com/state/washington/) - [Wisconsin](https://isitonrecall.com/state/wisconsin/) - [West Virginia](https://isitonrecall.com/state/west-virginia/) - [Wyoming](https://isitonrecall.com/state/wyoming/) ## Dates in the source - **Report date**: Sep 11, 2024 - **Recall initiation date**: Jul 16, 2024 - **Center classification date**: Sep 4, 2024 FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable. ## What to do next Read the official notice for the action that applies to your exact product. [Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2942-2024%22) ## Related records [Medical devices records](https://isitonrecall.com/category/medical-devices/) [Philips Respironics, Inc. records](https://isitonrecall.com/brand/philips-respironics-inc/)