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Philips Medical Systems Sales & Service Region No. America

Philips Medical Systems Sales & Service Region No. America Recalls

All product recalls associated with Philips Medical Systems Sales & Service Region No. America.

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Recall Summary

Total Recalls

416

Past Year

Class I (Serious)

Most Recent

Oct 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 401–416 of 416 recalls

Philips Medical Systems Sales & Service Region No. America: Bucky Diagnost FS Part number 9890-010-83651

Support chain attachment on the Bucky carriage may fail and cause the counter weights or X-ray tube to fall.

FDANov 18, 2003CA, FL, IN +1 more• Philips Medical Systems Sales & Service Region No. America

Philips Medical Systems Sales & Service Region No. America: Clea Stand Ceiling used with the Integris X-Ray System H5...

The cable carrier and cables may fall after repeat collisions with OR lamps, radiation shields or other supported accessories.

FDAOct 10, 2003Nationwide• Philips Medical Systems Sales & Service Region No. America

Philips Medical Systems Sales & Service Region No. America: Monitor Ceiling Suspension for Fluoroscopic and Angiograp...

The thumbscrew hinge pin on the monitor support arm could become loose allowing the monitor to fall.

1...19 2021

Page 21 of 21Next

FDA

Oct 10, 2003

Nationwide

• Philips Medical Systems Sales & Service Region No. America

Philips Medical Systems (Cleveland) Inc: Philips Odyssey FX Workstations, used with Axis, Irix, or...

Due to a software anomaly, an incorrect patient name may be transmitted with image to Odyssey workstation.

FDASep 15, 2003Nationwide• Philips Medical Systems (Cleveland) Inc

Philips Medical Systems (Cleveland) Inc: Philips Odyssey LX Workstations, used with Axis, Irix, o...

Due to a software anomaly, an incorrect patient name may be transmitted with image to Odyssey workstation.

FDASep 15, 2003Nationwide• Philips Medical Systems (Cleveland) Inc

Philips Medical Systems (Cleveland) Inc: Philips Odyssey VP Workstations, used with Axis, Irix, or...

Due to a software anomaly, an incorrect patient name may be transmitted with image to Odyssey workstation.

FDASep 15, 2003Nationwide• Philips Medical Systems (Cleveland) Inc

Philips Medical Systems: Model M4735A HeartStart XL Defibrillator//Monitor

Instructions For Use include addtional information on configuration for selecting Power on Lead

FDASep 2, 2003Nationwide• Philips Medical Systems

Philips Medical Systems Sales & Service Region No. America: Diagnost 94

Potential for table to move by itself

FDAAug 10, 2003Nationwide• Philips Medical Systems Sales & Service Region No. America

Philips Medical Systems Sales & Service Region No. America: Diagnost 97

Potential for table to move by itself

FDAAug 10, 2003Nationwide• Philips Medical Systems Sales & Service Region No. America

Philips Medical Systems Sales & Service Region No. America: Diagnost 96

Potential for table to move by itself

FDAAug 10, 2003Nationwide• Philips Medical Systems Sales & Service Region No. America

Philips Medical Systems Sales & Service Region No. America: OmniDiagnost System

Labeling of push button caps located on the control panel may not clearly identify the applied Source to Image distance (SID).

FDAJul 17, 2003Nationwide• Philips Medical Systems Sales & Service Region No. America

Philips Medical Systems Sales & Service Region No. America: Diagnost 97

Labeling of push button caps located on the control panel may not clearly identify the applied Source to Image distance (SID).

FDAJul 17, 2003Nationwide• Philips Medical Systems Sales & Service Region No. America

Philips Medical Systems: Easy Access Software releases 1.1, 5.2, 6.2 & 7.2

If DICOM fields for body part, description or accession number are changed, change won't update on the EasyWeb client or hospital systems.

FDAJun 27, 2003Nationwide• Philips Medical Systems

Philips Medical Systems (Cleveland) Inc: Intinion 1.5 T MRI Scanner.

There is a potential for the patient to be exposed to cryogenic fluids (liquid air) dripping from the vent during a quench due to the location of the vent.

FDAApr 17, 2003Nationwide• Philips Medical Systems (Cleveland) Inc

Philips Medical Systems (Cleveland) Inc: Philips MX8000 Dual v. EXP CT Scanner, utilizing V2.0 sof...

Patient images may be incorrectly stored in the archive directory of a different patient.

FDAApr 2, 2003Nationwide• Philips Medical Systems (Cleveland) Inc

Philips Medical Systems (Cleveland) Inc: Philips MX8000 IDT CT Scanner, utilizing V2.1 software.

Patient images may be incorrectly stored in the archive directory of a different patient.

FDAApr 2, 2003Nationwide• Philips Medical Systems (Cleveland) Inc