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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-2893-2026
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Philips Allura, Cardio Vascular-Allura Centron. Model Number: 722400. Interventional Fluoroscopic... 2 08/05/2026 FEI # 3042175844
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
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