FDA-Device2026-01-21Class IIPROCESSING DEFECT

Philips Allura Xper FD10/10 X-ray system recalled for missing cooling drip tray

ELECTRICAL SHOCKFIRENationwide distribution

Check your Philips Allura Xper FD10/10 system

Philips has identified that some Allura Xper FD10/10 X-ray systems may be missing a drip tray that was supposed to be installed beneath the cooling unit during a previous service. Without this tray, coolant liquid could contact electrical components and cause a short circuit, potentially shutting down the system.

  • Check if your system's serial number matches the affected list (298, 246, 146, 170, 238, 162, 7, 99, 81, 126, 55, 86, 6, 259, 205, 60, 57, 63, 145, 182, 48, 278)
  • Contact Philips Medical Systems to verify whether the drip tray was properly installed
  • Request Philips to install or document installation of the drip tray if needed
Hazard

Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown.

Sold states
Worldwide distribution - US Nationwide and the countries of Argentina, Australia, Bangladesh, Belgium, Brazil, Cayman Islands, Chile, China, Colombia, Costa Rica, Cuba, Czech Republic, Denmark, Dominican Republic, Ecuador, Egypt, France, Germany, Greece, Guatemala, Honduras, India, Italy, Japan, Kenya, Korea, Republic of, Malaysia, Mexico, Nepal, Netherlands, Oman, Pakistan, Panama, Paraguay, Peru, Philippines, Poland, Qatar, Romania, Russian Federation, Saudi Arabia, Singapore, South Africa, Spain, Sri Lanka, Switzerland, Taiwan, Thailand, Turkey, United Arab Emirates, United Kingdom, Venezuela, Yemen.
Affected count
22 units
Manufactured in
Veenpluis 4-6, Best, Netherlands
Products
Allura Xper FD10/10; Model Number: 722027;

Official notice

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1074-2026

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