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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-0015-2026
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Cardio Vascular-Allura Centron; Model Numbers: 722400; Associated 510(k)s: K102005, K130638, K1308... 2 10/01/2025 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
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