Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K102985 |
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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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| Philips Respironics V60 Ventilator (All Models, including: 1053613, 1053614, 1053615, 1053616, 10536... | 1 | 04/18/2022 |
FEI # 2518422 Respironics California, LLC |
| Philips Respironics V60 Plus Ventilator (All Models, including: 1138747, 1137276) | 1 | 04/18/2022 |
FEI # 2518422 Respironics California, LLC |
| Philips Respironics V60 Plus Ventilator Part Number 1138747 | 1 | 02/25/2022 |
FEI # 2518422 Respironics California, LLC |
| Philips Respironics V60 Ventilator Part Number 1053617 | 1 | 02/25/2022 |
FEI # 2518422 Respironics California, LLC |
| Philips V60 Ventilator with Version 2.20 Software, Description: V 60 Ventilator,Intl Opt: CFLEX... | 2 | 03/27/2017 |
FEI # 2518422 Respironics California Inc |
| Philips Respironics V60/V60 Plus Ventilator, PCBA Part Number: 453561544461 V60 Device Part N... | 1 | 09/28/2023 |
FEI # 2518422 Philips Respironics, Inc. |
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