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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 64 Results
Related Medical Device Recalls
 
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Z-0869-2019 - Prodiva CS, Model Number 781069. Nuclear Magnetic Resonance Imaging System 2 02/22/2019 FEI # 3002807880
Philips Medical Systems Nederlands
Z-0932-2019 - Multiva 1.5T, Model Number 781076. Nuclear Magnetic Resonance Imaging System 2 02/22/2019 FEI # 3002807880
Philips Medical Systems Nederlands
Z-0871-2019 - Multiva 1.5T 8 R5 (ZBO), Model Number 781072. Nuclear Magnetic Resonance Imaging System 2 02/22/2019 FEI # 3002807880
Philips Medical Systems Nederlands
Z-0872-2019 - Multiva 1.5T 16 R5 (ZBO), Model Number 781073. Nuclear Magnetic Resonance Imaging System 2 02/22/2019 FEI # 3002807880
Philips Medical Systems Nederlands
Z-0873-2019 - Multiva 1.5T 16 R5, Model Number 781078. Nuclear Magnetic Resonance Imaging System 2 02/22/2019 FEI # 3002807880
Philips Medical Systems Nederlands
Z-0874-2019 - Intera 0.5T Standard, Model Number 781101. Nuclear Magnetic Resonance Imaging System 2 02/22/2019 FEI # 3002807880
Philips Medical Systems Nederlands
Z-0875-2019 - Intera 1.0T Omni/Stellar, Model Number 781102. Nuclear Magnetic Resonance Imaging System 2 02/22/2019 FEI # 3002807880
Philips Medical Systems Nederlands
Z-0876-2019 - Intera 1.0T Power/Pulsar, Model Number 781103. Nuclear Magnetic Resonance Imaging System 2 02/22/2019 FEI # 3002807880
Philips Medical Systems Nederlands
Z-0877-2019 - Intera 1.5T Omni/Stellar, Model Number 781104. Nuclear Magnetic Resonance Imaging System 2 02/22/2019 FEI # 3002807880
Philips Medical Systems Nederlands
Z-0878-2019 - Intera 1.5T Power/Pulsar, Model Number 781105. Nuclear Magnetic Resonance Imaging System 2 02/22/2019 FEI # 3002807880
Philips Medical Systems Nederlands
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