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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-2632-2025
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Allura Xper FD20/10; Product Code: 722029; Associated 510(k) numbers: K102005, K130842, K130638, K13... 2 09/25/2025 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
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