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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-2189-2025
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Philips Allura R8.2.x Systems. Software Verion: R8.2.x. 1. Allura Xper FD10, Model Number: 72202... 2 07/29/2025 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
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