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U.S. Department of Health and Human Services

Medical Device Recalls
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71 to 80 of 168 Results
Class 1 Recall Date from: 01/01/2022 Recall Date to: 12/31/2022
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Baxter CLEARLINK System, Non-DEHP Solution Set with DUO-VENT Spike, Product Code 2R8403. An in-line... 1 09/14/2022 Baxter Healthcare Corporation
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 A30, Rx Only. To provide noninvasive ventilation support for patients with obstructiv... 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.
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.
NIM CONTACT EMG Endotracheal Tube, Part Numbers: a) REF 8229508 b) REF 8229507 c) REF 8229506 1 09/01/2022 Medtronic Xomed, Inc.
NIM EMG Endotracheal Tube, Part Numbers: a) REF 8229308 b) REF 8229307 c) REF 8229306 1 09/01/2022 Medtronic Xomed, Inc.
NIM EMG Endotracheal Tube, Part Numbers: a) REF 8229307J b) REF 8229308J c) REF 8229306J 1 09/01/2022 Medtronic Xomed, Inc.
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