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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 4 of 4 Results
Related Medical Device Recalls
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Product Description
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FDA Recall
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Z-3040-2026 - Philips Brilliance. Models: Brilliance iCT, Brilliance iCT Upgrades, Brilliance iCT SP. Software 4.1.10.x Product Codes: 728306, 728305, 728311. 2 09/01/2026 FEI # 3016618143
Philips North America Llc
Z-3043-2026 - Philips Brilliance CT 64: Brilliance CT 64 Channel Product Code: 728231, Brilliance CT 64 Upgrades Product Code: 728232. Software 4.1.10.x 2 09/01/2026 FEI # 3016618143
Philips North America Llc
Z-3042-2026 - Philips Ingenuity CT Product Codes: Ingenuity CT Upgrades 728327, Ingenuity CT China 728324, Ingenuity Core 128 Elite Brazil 728325. Software 4.4.10.x 2 09/01/2026 FEI # 3016618143
Philips North America Llc
Z-3041-2026 - Philips IQon Spectral CT Product Codes: IQon Spectral CT 728332, IQon Spectral CT 728331 Software 4.7.7.x 2 09/01/2026 FEI # 3016618143
Philips North America Llc
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