Philips North America Llc recalls
28 recalls.
- Philips Medical Systems Technologies Ltd. Spectral CT 7500 recall (Philips North America Llc)
Medical deviceClass IIReported October 7, 2026 · The Bolus tracking scan application may crash with a system error message. Bolus Tracker shots may continue to occur even if the contrast threshold is reached.... - SmartPath to dStream for 1.5T recall (Philips North America Llc)
Medical deviceClass IIReported September 30, 2026 · A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction... - MR 7700 and Upgrade to MR 7700 recall (Philips North America Llc)
Medical deviceClass IIReported September 30, 2026 · A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction... - MR 5300 Model Number recall (Philips North America Llc)
Medical deviceClass IIReported September 30, 2026 · A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction... - Name recall (Philips North America Llc)
Medical deviceClass IIReported September 30, 2026 · A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction... - Ingenia Elition S and Ingenia Elition X recall (Philips North America Llc)
Medical deviceClass IIReported September 30, 2026 · A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction... - Ingenia 3.0T and Ingenia 3.0T CX recall (Philips North America Llc)
Medical deviceClass IIReported September 30, 2026 · A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction... - Ingenia Ambition S and Ingenia Ambition X recall (Philips North America Llc)
Medical deviceClass IIReported September 30, 2026 · A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction... - Ingenia 1.5T recall (Philips North America Llc)
Medical deviceClass IIReported September 30, 2026 · A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction... - Evolution upgrade 1.5T and Evolution upgrade 3.0T recall (Philips North America Llc)
Medical deviceClass IIReported September 30, 2026 · A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction... - Achieva XR recall (Philips North America Llc)
Medical deviceClass IIReported September 30, 2026 · A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction... - Achieva 3.0T recall (Philips North America Llc)
Medical deviceClass IIReported September 30, 2026 · A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction... - Achieva 1.5T recall (Philips North America Llc)
Medical deviceClass IIReported September 30, 2026 · A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction... - Philips Brilliance CT 64: Brilliance CT 64 Channel Product Code: 728231 recall (Philips North America Llc)
Medical deviceClass IIReported September 9, 2026 · Philips has identified an unintended radiation issue with the Philips IQon, iCT, Ingenuity, and Brilliance CT 64 systems that could affect the performance of... - Philips Ingenuity CT Product Codes: Ingenuity CT Upgrades 728327 recall (Philips North America Llc)
Medical deviceClass IIReported September 9, 2026 · Philips has identified an unintended radiation issue with the Philips IQon, iCT, Ingenuity, and Brilliance CT 64 systems that could affect the performance of... - Philips IQon Spectral CT Product Codes: IQon Spectral CT 728332 recall (Philips North America Llc)
Medical deviceClass IIReported September 9, 2026 · Philips has identified an unintended radiation issue with the Philips IQon, iCT, Ingenuity, and Brilliance CT 64 systems that could affect the performance of... - Philips Brilliance. Models: Brilliance iCT recall (Philips North America Llc)
Medical deviceClass IIReported September 9, 2026 · Philips has identified an unintended radiation issue with the Philips IQon, iCT, Ingenuity, and Brilliance CT 64 systems that could affect the performance of... - Cardiac Workstation 7000. Product Number: 860441. recall (Philips North America Llc)
Medical deviceClass IIReported August 26, 2026 · Device will intermittently provide inaccurate data related to native heart rate. - Cardiac Workstation 5000. Product Number: 860439. recall (Philips North America Llc)
Medical deviceClass IIReported August 26, 2026 · Device will intermittently provide inaccurate data related to native heart rate. - Philips Telemetry Monitor 5500 1.4 GHz. Model Number: 867232. Includes the following... recall (Philips North America Llc)
Medical deviceClass IIReported July 1, 2026 · Potential for device reset to default "NEW_DEVICE" state, which may lead to a to loss of device configuration and the equipment label, resulting in a failure... - Philips Avalon Fetal Monitor recall (Philips North America Llc)
Medical deviceClass IIReported July 1, 2026 · Monitor has incorrect assembly of the speaker connector which can cause device cables to be pulled out of the housing and increase the risk of intermittent or... - Philips Avalon Fetal Monitor recall (Philips North America Llc)
Medical deviceClass IIReported July 1, 2026 · Monitor has incorrect assembly of the speaker connector which can cause device cables to be pulled out of the housing and increase the risk of intermittent or... - DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035. recall (Philips North America Llc)
Medical deviceClass IIReported June 17, 2026 · System was delivered without the required Seismic kit for Wall Stand VS2, which is designed to prevent damage and ensure stability of the Wall Stand VS2 during... - Spectral CT 7500 on Rails recall (Philips North America Llc)
Medical deviceClass IIReported February 18, 2026 · As part of the CT systems sub assembly, thirty-two (32) fasteners are used to attach the rotor to the bearing within the gantry. One or more of these fasteners... - Spectral CT recall (Philips North America Llc)
Medical deviceClass IIReported February 18, 2026 · As part of the CT systems sub assembly, thirty-two (32) fasteners are used to attach the rotor to the bearing within the gantry. One or more of these fasteners... - IQon Spectral CT recall (Philips North America Llc)
Medical deviceClass IIReported February 18, 2026 · As part of the CT systems sub assembly, thirty-two (32) fasteners are used to attach the rotor to the bearing within the gantry. One or more of these fasteners... - Brilliance iCT recall (Philips North America Llc)
Medical deviceClass IIReported February 18, 2026 · As part of the CT systems sub assembly, thirty-two (32) fasteners are used to attach the rotor to the bearing within the gantry. One or more of these fasteners... - Philips Smart-hopping 2.0 AP 1.4 GHz. Patient Monitor. recall (Philips North America Llc)
Medical deviceClass IIReported January 14, 2026 · It was found that the MX40 device could not reconnect to the PIC iX when moving between Radiohead and Trident 1.4 GHz access points if the signal strength...