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U.S. Department of Health and Human Services

Medical Device Recalls

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121 to 130 of 168 Results
Class 1 Recall Date from: 01/01/2022 Recall Date to: 12/31/2022
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Product Description
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Philips BiPAP A30, Rx Only. To provide noninvasive ventilation support for patients with obstructiv... 1 09/09/2022 Philips Respironics, Inc.
Philips OmniLab Advanced + with Heated Tube Humidifier, Rx Only. To provide noninvasive ventilation... 1 09/09/2022 Philips Respironics, Inc.
Philips OmniLab Advanced+ Intl (Flow Gen), Rx Only. To provide noninvasive ventilation support for ... 1 09/09/2022 Philips Respironics, Inc.
Philips OmniLab Advanced+, Rx Only. To provide noninvasive ventilation support for patients with ob... 1 09/09/2022 Philips Respironics, Inc.
Philips BiPAP V30 Auto, Rx Only. To provide noninvasive ventilation support for patients with obstr... 1 09/09/2022 Philips Respironics, Inc.
Philips BiPAP A40, Rx Only. To provide noninvasive ventilation support for patients with obstructiv... 1 09/09/2022 Philips Respironics, Inc.
Trilogy 100, Trilogy 200, Garbin Plus, Aeris, LifeVent Continuous Ventilators The device is inten... 1 03/18/2022 Philips Respironics, Inc.
Trilogy Evo Repair Kit, RP-Trilogy Evo Muffler Assembly, Material Number 1135257 The Trilogy Evo ... 1 01/22/2022 Philips Respironics, Inc.
Trilogy Evo, Material Numbers DS2110X11B (USA) and KR2110X15B (Korea) The Trilogy Evo ventilator ... 1 01/22/2022 Philips Respironics, Inc.
Thermo SCIENTIFIC, Sensititre GN7F, Gram Negative IVD AST 1 12/08/2022 Remel Inc
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