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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 14 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-1780-2025 - Intera 3.0T Quasar Dual, Model Number: 781150; 2 05/15/2025 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Z-1781-2025 - Intera CV, Model Number: 781107; 2 05/15/2025 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Z-1782-2025 - SmartPath to dStream for 1.5T, Model Number: 782146; 2 05/15/2025 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Z-1776-2025 - Intera 1.5T Master/Nova, Model Number: 781106; 2 05/15/2025 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
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