Reported Apr 12, 2023 · Ongoing
Trilogy EV300 Portable Electric Ventilator, Model Numbers DS2200X11B, IN2200X15B, FX2200X15B, CA2200X12B, CN2200X17B,…
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 EV300 Portable Electric VentilatorModel Numbers DS2200X11BIN2200X15BFX2200X15BCA2200X12BCN2200X17BBR2200X18BKR2200X15BIA2200X15BFR2200X14BND2200X15BIT2200X21BES2200X15BDE2200X13BBL2200X15BGB2200X15BEU2200X15BEU2200X19EE2200X15BTR2200X15BRU2200X15B
- Lot codes and dates
- UDI-DI
606959052017606959056497606959061033606959052321606959058613606959058620606959058644606959058668606959058675606959058682606959058705606959058798606959052000. UDI-DI
- Model numberSerial numbers 606959052017
- DS2200X11B
2,021 of 2,021 codes
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
- UDI-DI
- Amount recalled
- 62826 total 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
Why it was recalled
Stop using this product now
The accuracy of delivered oxygen may deviate below the required tolerance of 5% from setpoint when providing high concentration oxygen therapy. Additionally, if equipped, the internal FiO2 sensor may indicate a value higher than the device is actually delivering. This may lead to under delivery of oxygen.
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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