Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K183364 |
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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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bellavista 1000 Ventilator, Catalogue Number 301.100.030; Continuous Use Ventilator | 2 | 06/15/2023 | Vyaire Medical |
bellavista 1000e Ventilator, Catalogue Number 301.100.130; Continuous Use Ventilator | 2 | 06/15/2023 | Vyaire Medical |
bellavista 1000 ventilator, Catalog #301.100.030 and bellavista 1000e ventilator, 301.100.130. Th... | 1 | 02/16/2022 | Vyaire Medical |
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