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Philips Medical Systems (Cleveland) Recalls
315 recalls on record · June 20, 2012 to September 24, 2025 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
April 25, 2018Medical DevicesFDA
Philips Medical Systems (Cleveland) Inc recalls Ingenuity CT - Model no. 728326, 728325, Computed Tomography X-Ray system Product Usage: Computed Tomography X-ray s
Hazard: Closing the Emergency Stop may disable the horizontal motor, allowing the couch top to move during patient load or unload activities.
April 25, 2018Medical DevicesFDA
Philips Medical Systems (Cleveland) Inc recalls Ingenuity Flex - Model no. 728317, Computed Tomography X-Ray system Product Usage: Computed Tomography X-ray systems
Hazard: Closing the Emergency Stop may disable the horizontal motor, allowing the couch top to move during patient load or unload activities.
April 25, 2018Medical DevicesFDA
Philips Medical Systems (Cleveland) Inc recalls Brilliance 64 with 4.1.7 XX026 software version model number 728231 Product Usage: Computed Tomography X-ray systems
Hazard: Surview scan with tube current lower than 30 mA is unable to be initialized.
April 25, 2018Medical DevicesFDA
Philips Medical Systems (Cleveland) Inc recalls Ingenuity TF PET/CT, Model No. 882442 Product Usage: The device is an integrated diagnostic X-ray Computed Tomograph
Hazard: Following a period of inactivity, the mass storage device may cause the acquisition console to become unresponsive. This may prevent an acquisition from proceeding.
March 14, 2018Medical DevicesFDA
Philips Medical Systems (Cleveland) Inc recalls IQon Spectral CT with 4.7.2 software version.- Model 728332, a Philips Computed Tomography X-Ray System
Hazard: 23 Software related issues for the IQon Spectral CT with 4.7.2 software version. These issues include: " Software errors that may result in CT spectral images misrepresentation or incorrect treatment; " Software errors that may result in partial set of images or inability to generate CT images.
March 14, 2018Medical DevicesFDA
Philips Medical Systems (Cleveland) Inc recalls Brilliance Big Bore Oncology CTwith 4.2.0 software version. Model #' 728243 Product Usage: Computed Tomography X-ra
Hazard: Software issues including: Software errors that may result in Extended Field of View check message not displayed when Field of View is set >600 mm for a paused scan; Request for change to automatically turn on the center x/y 0 setting and the disable result rotation setting when turning on the CT simulation Exam Card; Software errors that may result in Tumor LOC allowing POI (Point of Interest) locking when a non-isocenter slice is displayed; Software errors that may result in partial set of images or inability to generate CT images.
March 14, 2018Medical DevicesFDA
Philips Medical Systems (Cleveland) Inc recalls Brilliance Big Bore Radiology CT with 4.2.0 software version. Model #' 728244 Product Usage: Computed Tomography X-r
Hazard: Software issues including: Software errors that may result in Extended Field of View check message not displayed when Field of View is set >600 mm for a paused scan; Request for change to automatically turn on the center x/y 0 setting and the disable result rotation setting when turning on the CT simulation Exam Card; Software errors that may result in Tumor LOC allowing POI (Point of Interest) locking when a non-isocenter slice is displayed; Software errors that may result in partial set of images or inability to generate CT images.
February 21, 2018Medical DevicesFDA
Philips Medical Systems (Cleveland) Inc recalls Ingenuity TF PET/CT (model 882442) running software version 4.0.2 This device is a diagnostic imaging system that c
Hazard: A software issue causes PET reconstructions to fail intermittently. It was determined that reconstructions fail due to a negative table position (-1 value is inserted) in the raw data list file, rather than the actual table position. This error has been found to occur in two scenarios: 1) When the system operator cancels an acquisition a. The error will occur every time a scan is cancelled by the operator. 2) Couch position requests within the software sequence were delayed a. The error occurs intermittently, but has been found to occur more frequently when the gantry s network is heavily loaded with multiple retrospective reconstructions running in parallel. b. The error manifests to the technologist by an error message and Failed status on the Reconstruction Monitor and the error message Result {0} failed to reconstruct" on the Acquisition Workflow window during reconstruction after the patient scan has been completed. In both scenarios, the acquisition data will not be able to be reconstructed and will therefore be unusable.
February 14, 2018Medical DevicesFDA
Philips Medical Systems (Cleveland) Inc recalls Ingenuity TF PET/CT - a integrated diagnostic X-ray Computed Tomography (CT) and Positron Emission Tomography (PET) syst
Hazard: One of the two wire channels mounted inside the Gantry Separation Unit (GSU) that is also used to secure the top two GSU covers, was missing mounting hardware.
February 14, 2018Medical DevicesFDA
Philips Medical Systems (Cleveland) Inc recalls Philips Ingenuity CT computed tomography x-ray system
Hazard: Numerous issues related to software Brilliance iCT 4.1.6 software version.
February 14, 2018Medical DevicesFDA
Philips Medical Systems (Cleveland) Inc recalls Philips Ingenuity Core 128 computed tomography x-ray system
Hazard: Numerous issues related to software Brilliance iCT 4.1.6 software version.
February 14, 2018Medical DevicesFDA
Philips Medical Systems (Cleveland) Inc recalls Philips Ingenuity Core computed tomography x-ray system
Hazard: Numerous issues related to software Brilliance iCT 4.1.6 software version.
February 14, 2018Medical DevicesFDA
Philips Medical Systems (Cleveland) Inc recalls Philips Brilliance 64 computed tomography x-ray system
Hazard: Numerous issues related to software Brilliance iCT 4.1.6 software version.
February 14, 2018Medical DevicesFDA
Philips Medical Systems (Cleveland) Inc recalls Precedence 16 Model # 882350 Product Usage: Precedence (cleared as Griffin) is an imaging system combining the acqui
Hazard: During collimator exchange, the alignment of the collimator cart and detectors may cause a collimator exchange fail, and a collimator may drop to the floor beside the collimator cart. The collimator may be partially supported by the cart (e.g. leaning against the cart), or it may fall/slide all the way to the floor.
February 14, 2018Medical DevicesFDA
Philips Medical Systems (Cleveland) Inc recalls Precedence 6 Model # 882351 Product Usage: Precedence (cleared as Griffin) is an imaging system combining the acquis
Hazard: During collimator exchange, the alignment of the collimator cart and detectors may cause a collimator exchange fail, and a collimator may drop to the floor beside the collimator cart. The collimator may be partially supported by the cart (e.g. leaning against the cart), or it may fall/slide all the way to the floor.
February 14, 2018Medical DevicesFDA
Philips Medical Systems (Cleveland) Inc recalls BrightView Model 882480 Product Usage: BrightView and BrightView X are gamma cameras designed for single or dual de
Hazard: During collimator exchange, the alignment of the collimator cart and detectors may cause a collimator exchange fail, and a collimator may drop to the floor beside the collimator cart. The collimator may be partially supported by the cart (e.g. leaning against the cart), or it may fall/slide all the way to the floor.
February 14, 2018Medical DevicesFDA
Philips Medical Systems (Cleveland) Inc recalls BrightView XCT Model 882482 Product Usage: BrightView XCT is a gamma camera for Single Photon Emission Computed Tomo
Hazard: During collimator exchange, the alignment of the collimator cart and detectors may cause a collimator exchange fail, and a collimator may drop to the floor beside the collimator cart. The collimator may be partially supported by the cart (e.g. leaning against the cart), or it may fall/slide all the way to the floor.
February 14, 2018Medical DevicesFDA
Philips Medical Systems (Cleveland) Inc recalls BrightView X, Model #882478 Product Usage: BrightView and BrightView X are gamma cameras designed for single or dua
Hazard: During collimator exchange, the alignment of the collimator cart and detectors may cause a collimator exchange fail, and a collimator may drop to the floor beside the collimator cart. The collimator may be partially supported by the cart (e.g. leaning against the cart), or it may fall/slide all the way to the floor.
January 31, 2018Medical DevicesFDA
Philips Medical Systems (Cleveland) Inc recalls Brilliance iCT - Model 728306 Computed Tomography X-ray systems
Hazard: Numerous software issues with Brilliance iCT 4.1.6 version. Issues affect scan start position, data acquisition, exam stop, tube overheat, memory overflow, failure to give error message, length of acquisition, image volume and other functions.
January 31, 2018Medical DevicesFDA
Philips Medical Systems (Cleveland) Inc recalls Brilliance iCT SP - Model 728311 Brilliance iCT - Model 728306 Computed Tomography X-ray systems
Hazard: Numerous software issues with Brilliance iCT 4.1.6 version. Issues affect scan start position, data acquisition, exam stop, tube overheat, memory overflow, failure to give error message, length of acquisition, image volume and other functions.
January 24, 2018Medical DevicesFDA
Philips Medical Systems (Cleveland) Inc recalls Ingenuity Core 128, (Code 728323) Intended to produce images of the head and body by computer reconstruction of x-ray
Hazard: Philips has identified that certain fasteners cannot be confirmed to have been torqued according to specification. If the fasteners were not torqued as specified and a failure occurs while the system is in use, the parts secured by the fasteners may become loose, which may have a potential for harm.
January 24, 2018Medical DevicesFDA
Philips Medical Systems (Cleveland) Inc recalls Ingenuity Core, (Code 728321) Intended to produce images of the head and body by computer reconstruction of x-ray tra
Hazard: Philips has identified that certain fasteners cannot be confirmed to have been torqued according to specification. If the fasteners were not torqued as specified and a failure occurs while the system is in use, the parts secured by the fasteners may become loose, which may have a potential for harm.
January 24, 2018Medical DevicesFDA
Philips Medical Systems (Cleveland) Inc recalls Brilliance 64, (Code 728231) Intended to produce images of the head and body by computer reconstruction of x-ray tran
Hazard: Philips has identified that certain fasteners cannot be confirmed to have been torqued according to specification. If the fasteners were not torqued as specified and a failure occurs while the system is in use, the parts secured by the fasteners may become loose, which may have a potential for harm.
January 24, 2018Medical DevicesFDA
Philips Medical Systems (Cleveland) Inc recalls Brilliance iCT Intended to produce images of the head and body by computer reconstruction of x-ray transmission data
Hazard: Philips has identified that certain fasteners cannot be confirmed to have been torqued according to specification. If the fasteners were not torqued as specified and a failure occurs while the system is in use, the parts secured by the fasteners may become loose, which may have a potential for harm.
January 17, 2018Medical DevicesFDA
Philips Medical Systems (Cleveland) Inc recalls Philips Healthcare IQon Spectral CT computed tomography x-ray system
Hazard: There is a possibility that screws holding an internal portion of the gantry (Reaction Ring) to the scanner s main bearing may come loose. If this occurs, the part(s) will not be expelled, however, a noise may be heard coming from the gantry.
January 17, 2018Medical DevicesFDA
Philips Medical Systems (Cleveland) Inc recalls Philips Healthcare Brilliance iCT SP computed tomography x-ray system
Hazard: There is a possibility that screws holding an internal portion of the gantry (Reaction Ring) to the scanner s main bearing may come loose. If this occurs, the part(s) will not be expelled, however, a noise may be heard coming from the gantry.
January 17, 2018Medical DevicesFDA
Philips Medical Systems (Cleveland) Inc recalls Philips Healthcare Brilliance iCT computed tomography x-ray system
Hazard: There is a possibility that screws holding an internal portion of the gantry (Reaction Ring) to the scanner s main bearing may come loose. If this occurs, the part(s) will not be expelled, however, a noise may be heard coming from the gantry.
April 12, 2017Medical DevicesFDA
Philips Medical Systems (Cleveland) Inc recalls BrightView X 3/8 model number 882478 BrightView and BrightView X are gamma cameras designed for single or dual detector
Hazard: The brake hub was not engaging with the gear box shaft due to an error in the assembly of components within the brake hub mechanism after service, causing the detector to backdrive.
April 12, 2017Medical DevicesFDA
Philips Medical Systems (Cleveland) Inc recalls BrightView X 3/4 model number 882479 BrightView and BrightView X are gamma cameras designed for single or dual detector
Hazard: The brake hub was not engaging with the gear box shaft due to an error in the assembly of components within the brake hub mechanism after service, causing the detector to backdrive.
April 12, 2017Medical DevicesFDA
Philips Medical Systems (Cleveland) Inc recalls BrightView XCT model number 882482 BrightView and BrightView X are gamma cameras designed for single or dual detector n
Hazard: The brake hub was not engaging with the gear box shaft due to an error in the assembly of components within the brake hub mechanism after service, causing the detector to backdrive.