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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 20 of 44 Results
510(K) Number: K082660
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FDA Recall
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Philips Respironics V60 Ventilator Part Number R1053618 - Product Usage: intended to be used only wi... 2 01/22/2021 FEI # 2518422
Respironics California, LLC
Philips Respironics V60 Ventilator Part Number 1076709 - Product Usage: intended to be used only wit... 2 01/22/2021 FEI # 2518422
Respironics California, LLC
Philips Respironics V60 Ventilator Part Number 1053618 - Product Usage: intended to be used only wit... 2 01/22/2021 FEI # 2518422
Respironics California, LLC
Philips Respironics V60 Ventilator Part Number 1053617 - Product Usage: intended to be used only wit... 2 01/22/2021 FEI # 2518422
Respironics California, LLC
Philips Respironics V60 Ventilator Part Number 1053616 - Product Usage: intended to be used only wit... 2 01/22/2021 FEI # 2518422
Respironics California, LLC
Philips Respironics V60 Ventilator Part Number 1053615 - Product Usage: intended to be used only wit... 2 01/22/2021 FEI # 2518422
Respironics California, LLC
Philips Respironics V60 Ventilator Part Number 1053614 - Product Usage: intended to be used only wit... 2 01/22/2021 FEI # 2518422
Respironics California, LLC
Philips Respironics V60 Ventilator Part Number 1053613 - Product Usage: intended to be used only wit... 2 01/22/2021 FEI # 2518422
Respironics California, LLC
Philips Respironics V60 Ventilator Part Number 1076717 - Product Usage: intended to be used only wit... 2 01/22/2021 FEI # 2518422
Respironics California, LLC
Philips Respironics V60 Plus Ventilator Part Number 1137276 - Product Usage: intended to be used onl... 2 01/22/2021 FEI # 2518422
Respironics California, LLC
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