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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-0676-2025
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Philips Allura Xper Systems (R7.6-R8.1). Labeled as the following: 1. Allura Xper FD10, Model Nu... 2 12/12/2024 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
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