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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-3041-2026
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Philips IQon Spectral CT Product Codes: IQon Spectral CT 728332, IQon Spectral CT 728331 Softwa... 2 09/01/2026 FEI # 3016618143
Philips North America Llc
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