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Philips Medical Systems (Cleveland) Inc

Philips Medical Systems (Cleveland) Inc Recalls

All product recalls associated with Philips Medical Systems (Cleveland) Inc.

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Recall Summary

Total Recalls

1000

Past Year

272

Class I (Serious)

Most Recent

Dec 2025

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 1061–1080 of 1137 recalls

Philips Medical Systems (Cleveland) Inc: Brilliance CT (computed tomography) scanners, Big Bore co...

Brilliance Big Bore- An anomaly was identified with software version 2.0 tumor localization application when printing work sheets. this causes information regarding relative locations of marked regions of interest on the patient work sheets to be incorrect and may cause mistreatment.

Class IIModerate

FDAApr 25, 2006CA, NV• Philips Medical Systems (Cleveland) Inc

Philips Medical Systems (Cleveland) Inc: Brilliance CT (computed tomography) scanners, Big Bore co...

FDAApr 25, 2006CA, NV• Philips Medical Systems (Cleveland) Inc

Philips Medical Systems North America Co. Phillips: MD4 X-ray system

1...52 535455 56 57

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Potential for unexpected table movement.

FDAApr 6, 2006Nationwide• Philips Medical Systems North America Co. Phillips

Philips Medical Systems North America Co. Phillips: MD3 X-ray system

Potential for unexpected table movement.

FDAApr 6, 2006Nationwide• Philips Medical Systems North America Co. Phillips

Plasma Flat Panel TVs (Philips) – Potential Defect (2006)

The recall involves only certain 42- and 50-inch, 2005 model Philips branded Plasma Flat Panel Televisions with Ambilight technology, which is an ambient lighting feature that projects a soft light onto the wall behind the TV to enhance the display. They were manufactured with the following model, date codes, and serial numbers: Model Display Type Production Began Production Ended Beginning Serial Range Ending Serial Range 42PF9630A/37 Plasma April 2005 July 2005 AG1A0518xxxxxx AG1A0528xxxxxx 50PF9630A/37 Plasma May 2005 August 2005 AG1A0519xxxxxx AG1A0533xxxxxx 50PF9630A/37 Plasma June 2005 August 2005 YA1A0523xxxxxx YA1A0534xxxxxx 50PF9830A/37 Plasma June 2005 August 2005 AG1A0526xxxxxx AG1A0533xxxxxx The model and serial numbers can be found on the back of the TV on the label that looks like the example in the picture: The serial number can also be obtained by pushing the following keystrokes on the remote control: 123654, after which a customer service menu ("CSM") will be displayed on the screen. In the menu, line 03 displays the type number and line 04 displays the production code (identical to the serial number of the set). Press the MENU button on the remote to exit the CSM.

CPSCMar 16, 2006Nationwide• Philips Consumer Electronics North America, of Atlanta, Ga.

Philips Medical Systems North America Co. Phillips: Allura Xper FD10 x-ray system

Potential lock-up of system requiring reboot of system.

FDAFeb 6, 2006Nationwide• Philips Medical Systems North America Co. Phillips

Philips Medical Systems North America Co. Phillips: Allura Xper FD10/10 x-ray system

Potential lock-up of system requiring reboot of system.

FDAFeb 6, 2006Nationwide• Philips Medical Systems North America Co. Phillips

Philips Medical Systems (Cleveland) Inc: Brilliance CT System 6/10/16/16P/40 configuration. No pa...

The system has a gap that can appear between the upper and lower tilt stand covers. The fingers may be squeezed if a person was to place them in this region while the gantry was tilting from an angle to zero tilt angle.

FDADec 27, 2005AZ, CO, GA +16 more• Philips Medical Systems (Cleveland) Inc

Philips Medical Systems (Cleveland) Inc: Brilliance CT System 6/10/16/16P/40 configuration. No pa...

Class IIModerate

FDADec 27, 2005AZ, CO, GA +16 more• Philips Medical Systems (Cleveland) Inc

Philips Medical Systems North America Co. Phillips: Gyroscan NT MRI System rev 4.x, 5.x, and 6.x software. S...

The Gyroscan NT MRI system has a computer software problem which results in images from one patient being placed into another patient's image record.

FDADec 9, 2005Nationwide• Philips Medical Systems North America Co. Phillips

Philips Medical Systems: HeartStart Pads Pediatric Plus, Pediatric Plus Multifun...

The Apex/Anterior and the Sternum/Posterior pad labels are located in reverse position to the wire and connector

FDANov 18, 2005Nationwide• Philips Medical Systems

Philips Medical Systems North America Co. Phillips: AD6 table for use with Integris and Integris Allura x-ray...

Potential for high voltage exposure involving the injector interface connector of patient support tables.

FDAOct 12, 2005Nationwide• Philips Medical Systems North America Co. Phillips

Philips Medical Systems North America Co. Phillips: AD6 table, modified, used with the XPER systems. The mo...

Potential for high voltage exposure involving the injector interface connector of patient support tables.

FDAOct 12, 2005Nationwide• Philips Medical Systems North America Co. Phillips

Philips Medical Systems North America Co. Phillips: AD5 table, modified, used with the XPER x-ray systems. ...

Potential for high voltage exposure involving the injector interface connector of patient support tables.

FDAOct 12, 2005Nationwide• Philips Medical Systems North America Co. Phillips

Philips Medical Systems North America Co. Phillips: AD5 table for use with Integris and Integris Allura x-ray...

Potential for high voltage exposure involving the injector interface connector of patient support tables.

FDAOct 12, 2005Nationwide• Philips Medical Systems North America Co. Phillips

Philips Medical Systems (Cleveland) Inc: Gemini GXL PET/CT Systems, 6, 10, 16 slice configurations...

The image balance center point correction algorithm used in CT image reconstruction may cause a disapperance or alteration of small circular anatomical structures that are both near the image center and perpendicular to the image plane. This artifact may lead to the misinterpretation of anatomy at the center of the image.

FDAAug 18, 2005IN• Philips Medical Systems (Cleveland) Inc

Philips Medical Systems North America Co. Phillips: Interis Allura BiPlane X-Ray System

1) During positioning of the Lateral Stand the rotation and/or skew movement may travel unexpectedly in opposite direction; 2) movement may be faster than normal speed; 3) the stand may not stop immediately upon release of the joystick.

FDAJul 27, 2005Nationwide• Philips Medical Systems North America Co. Phillips

Philips Ultrasound, Inc.: Envisor, M2540 Diagnostic Ultrasound System

A defect in the software allows incorrect measurement results to be entered into the system's built-in report.

FDAMay 13, 2005Nationwide• Philips Ultrasound, Inc.

Philips Ultrasound, Inc.: Philips HDI 4000 Ultrasound System Part numbers 9896 05...

The acoustic display of Mechanical Index and Thermal Index is inaccurate - two transducers may exceed limits for acoustic intensity and MI.

FDAMay 6, 2005Nationwide• Philips Ultrasound, Inc.

Philips Medical Systems North America Co. Phillips: View Forum 2003 software, SW 3.4L1

Automated analysis of vascular obstruction tool in software gives unreliable calibration and analysis results when using unprocessed images acquired on the Philips Allura FD10.

FDAApr 29, 2005Nationwide• Philips Medical Systems North America Co. Phillips