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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 14 Results
Related Medical Device Recalls
 
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Product Description
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Recall
Class
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FDA Recall
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Z-1770-2025 - Enterprise 1.5T, Model Number: 781145; 2 05/15/2025 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Z-1771-2025 - Intera 0.5T Standard, Model Number: 781101; 2 05/15/2025 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Z-1772-2025 - Intera 1.0T Omni/Stellar, Model Number: 781102; 2 05/15/2025 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Z-1773-2025 - Intera 1.0T Power/Pulsar, Model Number: 781103; 2 05/15/2025 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Z-1774-2025 - Intera 1.5T, Model Numbers: 781195 and 781295; 2 05/15/2025 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Z-1775-2025 - Intera 1.5T Explorer/Nova Dual, Model Number: 781108; 2 05/15/2025 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Z-1783-2025 - SmartPath to dStream for 3.0T, Model Number: 782145; 2 05/15/2025 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Z-1777-2025 - Intera 1.5T Omni/Stellar, Model Number: 781104; 2 05/15/2025 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Z-1778-2025 - Intera 1.5T Power/Pulsar, Model Number: 781105; 2 05/15/2025 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Z-1779-2025 - Intera 1.5T R11, Model Number: 781170; 2 05/15/2025 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
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