Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K113053 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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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. |
A-Series BiPAP Hybrid A30 (not marketed in US), A-Series BiPAP V30 Auto Continuous Ventilator, Minim... | 1 | 07/15/2021 | Philips Respironics, Inc. |
A-Series BiPAP A 40, A-Series BiPAP A30 Continuous Ventilator, Non-life Supporting | 1 | 07/15/2021 | Philips Respironics, Inc. |
DreamStation ASV, DreamStation ST, AVAPS, SystemOne ASV4, C-Series ASV, C-Series S/T and AVAPS, Omni... | 1 | 07/13/2021 | Philips Respironics, Inc. |
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