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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 10 of 30 Results
Related Medical Device Recalls
 
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Product Description
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Z-1836-2024 - Achieva 1.5T- Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device Model Number (REF): (1) 781296 (2) 781343 2 05/17/2024 Philips North America Llc
Z-1865-2024 - Upgrade dStream - Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device Model Number (REF): 782127 2 05/17/2024 Philips North America Llc
Z-1838-2024 - Achieva 1.5T Initial system Model Number (REF): 781178 2 05/17/2024 Philips North America Llc
Z-1839-2024 - Achieva 3.0T Model Number (REF): (1) 781345; (2) 781344; (3) 781278; (4) 781277; (5) 781177 2 05/17/2024 Philips North America Llc
Z-1840-2024 - Achieva 3.0T for PET -Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device Model Number (REF): 781477 2 05/17/2024 Philips North America Llc
Z-1841-2024 - Achieva 3.0T TX for PET Model Number (REF): 781479 2 05/17/2024 Philips North America Llc
Z-1842-2024 - AchievaXR -Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device Model Number (REF): 781253 2 05/17/2024 Philips North America Llc
Z-1843-2024 - Evolution upgrade 1.5T- Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device Model Number (REF): (1) 782116; (2) 782148 2 05/17/2024 Philips North America Llc
Z-1844-2024 - Evolution upgrade 3.0T Model Number (REF): (1)782117; (2) 782143 2 05/17/2024 Philips North America Llc
Z-1845-2024 - Ingenia 1.5T Model Number (REF): (1) 782140; (2) 782115; (3) 782101; (4) 781396; (5) 781341; (6) 781315 2 05/17/2024 Philips North America Llc
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