Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K131982 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| DreamStation Auto CPAP. Non-Continuous Ventilator. | 1 | 08/08/2025 | Philips Respironics, Inc. |
| DreamStation Auto BiPAP. Non-Continuous Ventilator. | 1 | 08/08/2025 | Philips Respironics, Inc. |
| DreamStation Auto. Non-Continuous Ventilator. | 1 | 08/08/2025 | Philips Respironics, Inc. |
| Philips DreamStation Auto BiPAP and CPAP, Model Numbers UCDSX500S11, UDSX500S11, UDSX500S11F, UDSX70... | 1 | 04/06/2023 | Philips Respironics, Inc. |
| SystemOne (Q-Series), DreamStation, DreamStation Go, Dorma 400, Dorma 500, REMstar SE Auto Nonconti... | 1 | 07/13/2021 | Philips Respironics, Inc. |
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