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Philips Respironics, Inc. Recall: Philips Trilogy 100 Ventilator, Model Numbers 1054260, 1

Philips Respironics, Inc. Recall: Philips Trilogy 100 Ventilator, Model Numbers 1054260, 1 is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Philips Respironics, Inc.; Product: Philips Trilogy 100 Ventilator, Model Numbers 1054260, 1054096, U1054260, U1054260B, 1054260B, CA1054096B, BT10

Recalling firmPhilips Respironics, Inc.
ProductPhilips Trilogy 100 Ventilator, Model Numbers 1054260, 1054096, U1054260, U1054260B, 1054260B, CA1054096B, BT1054260, 1054096B, R1054260, RSL1054260, CA1054096, R1054260B, R1054655TPV, AU1054096, AU1054096B, 1054096B, 1054097, BR1054096, LA1054096, CN1054096, KO1054096, KR1054096, R1054655TP, R1054655B, 1054655, 1054655TPV, 1054655TP, 1054655B
Reason for recallThe replacement silicone sound abatement foam installed into some Trilogy 100 and Trilogy 200 devices may separate from the plastic backing to which it is attached. If this were to happen, the foam could potentially block air inlet, which could result in a reduction in delivered therapy volume or pressure and could cause the device to alarm.
ClassificationClass I (most serious — reasonable probability of serious health consequences or death)
StatusOngoing
DistributionUS Nationwide and Global Distribution to countries of: Australia, Brazil, Canada, China, Germany, Japan, Korea, and Latin America.
Recall initiated20221207
Recall numberZ-0882-2023
Categorydevice
StatePA
CountryUnited States

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