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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 12 Results
Related Medical Device Recalls
 
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Product Description
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Z-0945-2024 - Achieva 1.5T. Model (REF) Numbers 781196, 781343, 781296. 2 02/01/2024 FEI # 3006648320
Philips North America
Z-0946-2024 - Achieva 1.5T Conversion. Model (REF) Numbers 781346, 781283. 2 02/01/2024 FEI # 3006648320
Philips North America
Z-0947-2024 - Achieva 1.5T Initial system. Model (REF) Numbers 781178. 2 02/01/2024 FEI # 3006648320
Philips North America
Z-0948-2024 - Achieva 3.0T. Model. (REF) Numbers 781277, 781177, 781278, 781344, 781345. 2 02/01/2024 FEI # 3006648320
Philips North America
Z-0949-2024 - Achieva XR. Model (REF) Numbers 781153, 781253. 2 02/01/2024 FEI # 3006648320
Philips North America
Z-0956-2024 - SmartPath to dStream for XR and 3.0T. Model (REF) Numbers 781270, 782113, 782129. 2 02/01/2024 FEI # 3006648320
Philips North America
Z-0951-2024 - Ingenia 3.0T CX. Model (REF) Numbers 781271, 782105. 2 02/01/2024 FEI # 3006648320
Philips North America
Z-0952-2024 - Intera 1.5T Achieva Nova. Model (REF) Numbers 781172. 2 02/01/2024 FEI # 3006648320
Philips North America
Z-0953-2024 - Intera 1.5T Achieva Nova-Dual. Model (REF) Number 781173. 2 02/01/2024 FEI # 3006648320
Philips North America
Z-0954-2024 - Intera Achieva 1.5T Pulsar. Model (REF) Number 781171. 2 02/01/2024 FEI # 3006648320
Philips North America
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