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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-2623-2025
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Allura Xper FD10 Product Codes: (1)722010, (2) 722026, (3) 722003; Associated 510(k) numbers: K10200... 2 09/25/2025 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
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