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U.S. Department of Health and Human Services

Medical Device Recalls
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31 to 40 of 41 Results
Related Medical Device Recalls
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Product Description
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FDA Recall
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Z-1580-2024 - Intera 1.5T Master/Nova, Magnetic Resonance System. 2 04/17/2024 Philips North America Llc
Z-1581-2024 - Intera 1.5T Omni/Stellar, Magnetic Resonance System. 2 04/17/2024 Philips North America Llc
Z-1582-2024 - Intera 1.5T Power/Pulsar, Magnetic Resonance System. 2 04/17/2024 Philips North America Llc
Z-1583-2024 - Intera 1.5T R11, Magnetic Resonance System. 2 04/17/2024 Philips North America Llc
Z-1584-2024 - Intera 3.0T Quasar Dual, Magnetic Resonance System. 2 04/17/2024 Philips North America Llc
Z-1585-2024 - Intera Achieva 1.5T Pulsar, Magnetic Resonance System. 2 04/17/2024 Philips North America Llc
Z-1586-2024 - Intera CV, Magnetic Resonance System. 2 04/17/2024 Philips North America Llc
Z-1587-2024 - MR 5300, Magnetic Resonance System. 2 04/17/2024 Philips North America Llc
Z-1588-2024 - MR 7700, Magnetic Resonance System. 2 04/17/2024 Philips North America Llc
Z-1589-2024 - SmartPath to dStream for 1.5T, Magnetic Resonance System. 2 04/17/2024 Philips North America Llc
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