Medical Device Recalls
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31 to 35 of 35 Results
510(K) Number: K181166 |
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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| Trilogy EV300. Model Numbers: DS2200X11B, IN2200X15B, BL2200X15B, BR2200X18B, CA2200X12B, DE2200X13B... | 1 | 11/13/2024 |
FEI # 2518422 Philips Respironics, Inc. |
| Philips Respironics Trilogy Evo, Software Version 1.05.15.00. Continuous home-use ventilator device. | 1 | 03/26/2026 |
FEI # 2518422 Philips Respironics, Inc. |
| Philips Respironics Trilogy Evo, Software Version 1.05.15.00. Continuous home-use ventilator device.... | 1 | 04/02/2026 |
FEI # 2518422 Philips Respironics, Inc. |
| Philips Respironics Trilogy Evo O2, Software Version 1.05.15.00. Continuous home-use ventilator devi... | 1 | 04/02/2026 |
FEI # 2518422 Philips Respironics, Inc. |
| Philips Respironics Trilogy EV300, Software Version 1.05.15.00. Continuous home-use ventilator devic... | 1 | 04/02/2026 |
FEI # 2518422 Philips Respironics, Inc. |
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