Reported Jun 14, 2023 · Ongoing
Trilogy Evo O2 EV300, Model Numbers DS2200X11B, IN2200X15B, FX2200X15B, CA2200X12B, FR2200X14B, ND2200X15B, ES2200X15B,…
Philips Respironics, Inc.
High riskUsing this product could cause serious injury, illness or death — stop using it now.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Philips Respironics, Inc. · 1001 Murry Ridge Ln · Murrysville, PA · 15668-8517
Is this the product you have?
Trilogy Evo O2 EV300Model Numbers DS2200X11BIN2200X15BFX2200X15BCA2200X12BFR2200X14BND2200X15BES2200X15BBL2200X15BGB2200X15BEU2200X15BEE2200X15Band TR2200X15B
- Lot codes and dates
- UDI-DI
606959052017606959056497606959061033606959052321606959058613606959058620606959058644606959058668606959058675606959058682606959058705606959058798
- Serial Numbers
2,316 of 2,316 codes
H800088856BDCH800088865947H80008889A1B0H800088913420H8000889206BBH800089218A54H295004989AF7H295005081733H29500526CDFDH29500537C5ACH29500543CE80H29500550E5C3H29500557917CH29500562ECB9H2950058276A9H29500589C87AH295005940A47H2950064102F6H29500644555BH2950064767C0H295006500AA7H295006566F91H295006577E18H295006599766H29500695F4AAH295007020DD1H29500710371BH29500716522DH295007210CFAH2950072769CCH295007333630H29500748C5EBH29500782C311H29500785B7AEH29500791E852H29500808E84CH295008107DDCH2950081618EAH295008304E6CH295008362B5AH295008400364H2950084554C9H2950086030D4H2950086213C6H29500867446BH295008731B97H29500878A544H29500881BB4DH29500883985FH29500885FD69H295109734A0FH295684188A77H29568454277BH295684894CE6H2956852613BDH295702706AAAH295702771E15H29570309E0BFH2957035666F0H295722010F5D
- UDI-DI
- Amount recalled
- 18,855 devices
This recall covers 4 products
The agency filed one notice per product. You are reading one of them; the other 3 are below.
Where it was sold
- Nationwide
Why it was recalled
Stop using this product now
Environmental debris may accumulate on the internal machine flow sensor causing partial occlusion which may impact accurate delivery of pressure, volume, or flow. A malfunction caused by this issue can result in patient harm up to hypoxemia if not addressed by the care provider.
Using this product could cause serious injury, illness or death — stop using it now.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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