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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-0597-2026
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Azurion R3.0. Model Number 722234. Commercial Name: Azurion 7 M20. INTERVENTIONAL FLUOROSCOPIC XR... 2 12/09/2025 FEI # 3006648320
Philips North America
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