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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 7 of 7 Results
Related Medical Device Recalls
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Product Description
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Class
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FDA Recall
Posting Date
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Recalling Firm
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Z-0389-2024 - Achieva 1.5T 2 11/21/2023 FEI # 3016618143
Philips North America Llc
Z-0390-2024 - Achieva 1.5T Conversion 2 11/21/2023 FEI # 3016618143
Philips North America Llc
Z-0391-2024 - Achieva 1.5T Initial System 2 11/21/2023 FEI # 3016618143
Philips North America Llc
Z-0395-2024 - SmartPath to dStream for 1.5T 2 11/21/2023 FEI # 3016618143
Philips North America Llc
Z-0393-2024 - Intera 1.5T 2 11/21/2023 FEI # 3016618143
Philips North America Llc
Z-0394-2024 - Intera 1.5T Power/Pulsar 2 11/21/2023 FEI # 3016618143
Philips North America Llc
Z-0392-2024 - Ingenia 1.5T CX 2 11/21/2023 FEI # 3016618143
Philips North America Llc
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