Medical Device Recalls
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41 to 44 of 44 Results
510(K) Number: K082660 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Respironics V60 Ventilator, Service # 850008, REF: 1053613, 1053614, 1053617, 1053614 | 2 | 03/02/2020 |
FEI # 2518422 Respironics California, LLC |
| Respironics RP-UI Assy, V60 Ventilators User Interface RP-Kits, REF/P/N: 453561528931, 4535615289... | 2 | 03/02/2020 |
FEI # 2518422 Respironics California, LLC |
| Respironics V60 Ventilator, manufactured by Respironics California Inc. in Carlsbad, CA. | 2 | 11/24/2010 |
FEI # 2518422 Respironics California Inc |
| RESPIRONICS V60 VENTILATOR | 2 | 11/11/2009 |
FEI # 2518422 Respironics California Inc |
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