Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K111610 |
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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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Trilogy 100, Trilogy 200, Garbin Plus, Aeris, LifeVent Continuous Ventilators The device is inten... | 1 | 03/18/2022 | Philips Respironics, Inc. |
Trilogy 100, Trilogy 200, Garbin Plus, Aeris, LifeVent Continuous Ventilators. | 1 | 07/15/2021 | Philips Respironics, Inc. |
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