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U.S. Department of Health and Human Services

Medical Device Recalls
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31 to 35 of 35 Results
510(K) Number: K181166
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Product Description
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FDA Recall
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Trilogy EVO Ventilator, International, Model Number IN2110X15B Trilogy Evo is intended for pediat... 1 02/15/2020 FEI # 2518422
Philips Respironics, Inc.
Trilogy EVO Ventilator, 02 - Iberia - Model Number: ES2100X15B Trilogy Evo is intended for pediat... 1 02/15/2020 FEI # 2518422
Philips Respironics, Inc.
Trilogy EVO Ventilator, 02 - EU - Model Number: EU2100X15B Trilogy Evo is intended for pediatric ... 1 02/15/2020 FEI # 2518422
Philips Respironics, Inc.
LifeVent EVO Ventilator, 02 - Model Number: SP2100X26B Trilogy Evo is intended for pediatric thro... 1 02/15/2020 FEI # 2518422
Philips Respironics, Inc.
Trilogy EVO Ventilator, France - Model Number: FR2110X14B Trilogy Evo is intended for pediatric t... 1 02/15/2020 FEI # 2518422
Philips Respironics, Inc.
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