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U.S. Department of Health and Human Services

Medical Device Recalls

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Related Medical Device Recalls
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Product Description
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FDA Recall
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Z-2412-2026 - Philips Allura Xper with the following Model Numbers: Model # 722001 for Allura Xper FD10C; Model # 722002 for Allura Xper FD10F; Model # 722003 for Allura Xper FD10; Model # 722005 for Allura Xper FD... 2 06/16/2026 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Z-2411-2026 - Philips MultiDiagnost Eleva with the following Model Numbers: Model # 708032 for MultiDiagnost Eleva; Model # 708034 for MultiDiagnost Eleva with Flat Detector; Model # 708036 for MultiDiagnost E... 2 06/16/2026 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
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