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U.S. Department of Health and Human Services

Medical Device Recalls
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41 to 50 of 64 Results
Related Medical Device Recalls
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Product Description
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FDA Recall
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Z-0911-2019 - Ingenia 3.0T, Model Number 781342. Nuclear Magnetic Resonance Imaging System 2 02/22/2019 FEI # 3002807880
Philips Medical Systems Nederlands
Z-0904-2019 - Ingenia 3.0T CX, Model Number 781271. Nuclear Magnetic Resonance Imaging System 2 02/22/2019 FEI # 3002807880
Philips Medical Systems Nederlands
Z-0919-2019 - Ingenia 1.5T, Model Number 781396. Nuclear Magnetic Resonance Imaging System 2 02/22/2019 FEI # 3002807880
Philips Medical Systems Nederlands
Z-0910-2019 - Ingenia 1.5T, Model Number 781341. Nuclear Magnetic Resonance Imaging System 2 02/22/2019 FEI # 3002807880
Philips Medical Systems Nederlands
Z-0916-2019 - Ingenia 1.5T S, Model Number 781347. Nuclear Magnetic Resonance Imaging System 2 02/22/2019 FEI # 3002807880
Philips Medical Systems Nederlands
Z-0901-2019 - Ingenia 1.5T CX, Model Number 781261. Nuclear Magnetic Resonance Imaging System 2 02/22/2019 FEI # 3002807880
Philips Medical Systems Nederlands
Z-0902-2019 - Ingenia 1.5T CX (ZBO), Model Number 781262. Nuclear Magnetic Resonance Imaging System 2 02/22/2019 FEI # 3002807880
Philips Medical Systems Nederlands
Z-0882-2019 - Enterprise 1.5T, Model Number 781145. Nuclear Magnetic Resonance Imaging System 2 02/22/2019 FEI # 3002807880
Philips Medical Systems Nederlands
Z-0884-2019 - Achieva XR 1.5T/3.0T, Model Number 781153. Nuclear Magnetic Resonance Imaging System 2 02/22/2019 FEI # 3002807880
Philips Medical Systems Nederlands
Z-0899-2019 - Achieva XR 1.5T/3.0T , Model Number 781253. Nuclear Magnetic Resonance Imaging System 2 02/22/2019 FEI # 3002807880
Philips Medical Systems Nederlands
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