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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
Recall Number: Z-0005-2026
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Allura Xper FD20; Model Numbers: (1) 722006, (2) 722012, (3) 722028; Associated 510(k)s: K102005, ... 2 10/01/2025 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
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