Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K121623 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| A-Series BiPAP A 40, A-Series BiPAP A30 Continuous Ventilator, Non-life Supporting | 1 | 07/15/2021 |
FEI # 2518422 Philips Respironics, Inc. |
| BiPAP A40 Ventilator. Used to provide noninvasive ventilation support for the purpose of treating ad... | 1 | 07/02/2025 |
FEI # 2518422 Philips Respironics, Inc. |
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