Philips North America Llc
437 federal recalls on file, showing the 162 from the last 12 months. We monitor every CPSC, FDA, USDA, and NHTSA notice for Philips North America Llc and translate it into plain English — free weekly digest, optional same-day alerts.
- 2026-01-21FDA-DeviceClass IICheck your Philips Allura Xper FD20/20 system
Philips identified that 8 Allura Xper FD20/20 X-ray systems may be missing a drip tray beneath the cooling unit due to incomplete installation or documentation during previous repairs. If the tray is not in place, coolant liquid could contact electrical components and cause a short circuit, potentially shutting down the system.
- 2026-01-21FDA-DeviceClass IICheck your Philips Allura Xper FD20/10 system
Philips identified that a small number of Allura Xper FD20/10 X-ray systems may be missing a drip tray that should be installed beneath the cooling unit. Without this tray, coolant liquid could contact electrical components and cause short-circuits, potentially shutting down the system.
- 2026-01-21FDA-DeviceClass IICheck your Philips Allura Xper FD20 system
Philips identified that in 2 Allura Xper FD20 X-ray systems, the drip tray under the cooling unit was not installed or not properly documented during previous maintenance. If missing, coolant liquid could contact electrical parts and cause a short circuit, leading to system shutdown.
- 2026-01-21FDA-DeviceClass IICheck 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.
- 2026-01-21FDA-DeviceClass IIAllura Xper FD10; Model Number: 722026;
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.
- 2026-01-21FDA-DeviceClass IICheck your Philips Allura Xper FD20 OR Table for drip tray
Philips identified that in a small number of operating room tables, a drip tray beneath the cooling unit may not have been installed during previous maintenance, or the installation was not properly documented. If missing, coolant could leak onto electrical components and cause a short circuit, potentially shutting down the system.
- 2026-01-21FDA-DeviceClass IICheck your Philips Allura Xper FD20 system
Philips identified that some Allura Xper FD20 Biplane X-ray systems may be missing a drip tray under the cooling unit, either from incomplete past repairs or undocumented installation. Without this tray, coolant liquid could leak onto electrical components and cause short-circuits that shut down the system.
- 2026-01-21FDA-DeviceClass IICheck your Philips Allura Xper FD20 system
Philips identified that some Allura Xper FD20 X-ray systems may be missing a drip tray beneath the cooling unit due to incomplete previous service work. If the tray is not installed, coolant can leak onto electrical components and cause a short circuit, potentially shutting down the system.
- 2026-01-21FDA-DeviceClass IICheck your Philips Allura Xper FD10/10 system
Philips identified that some Allura Xper FD10/10 X-ray systems may be missing a drip tray that protects electrical components from coolant liquid. If the tray was not installed during a previous service, coolant could contact electrical parts and cause a short circuit, potentially shutting down the system.
- 2026-01-21FDA-DeviceClass IICheck your Philips Allura Xper FD10 system
Philips identified that in 56 X-ray systems worldwide, a drip tray beneath the cooling unit may not have been installed during previous maintenance, or the installation may not have been properly documented. If missing, coolant liquid could contact electrical components and cause a short circuit, potentially shutting down the system.
- 2026-01-21FDA-DeviceClass IICheck your Philips Allura Xper FD20 system
Philips has identified that 18 Allura Xper FD20 Biplane X-ray systems worldwide may be missing a drip tray beneath the cooling unit due to incomplete field repairs or missing documentation. Without this tray, coolant liquid could contact electrical components and cause short circuits that shut down the system.
- 2026-01-21FDA-DeviceClass IICheck your Philips Allura Xper FD20 system
Philips identified that some Allura Xper FD20 X-ray systems may be missing a drip tray beneath the cooling unit from previous service work. Without this tray, coolant could leak onto electrical components and cause a short circuit, potentially shutting down the system during use.
- 2026-01-21FDA-DeviceClass IICheck your Philips Allura Xper FD10/10 system
Philips identified that 14 of their Allura Xper FD10/10 X-ray systems may be missing a drip tray beneath the cooling unit. Without this tray, coolant liquid could contact electrical parts and cause a short-circuit, potentially shutting down the system.
- 2026-01-21FDA-DeviceClass IICheck your Philips Allura Xper FD10 system
Philips identified that some Allura Xper FD10 X-ray systems may be missing a drip tray beneath the cooling unit due to incomplete field repairs. If the tray is not in place, coolant can leak onto electrical components and cause short-circuits, potentially shutting down the system.
- 2026-01-21FDA-DeviceClass IICheck your Philips Allura Xper FD10F system
Philips identified that some Allura Xper FD10F imaging systems may be missing a drip tray beneath the cooling unit due to incomplete field corrections. If the drip tray is not in place, coolant liquid could contact electrical components and cause short-circuits, potentially shutting down the system.
- 2026-01-21FDA-DeviceClass IIContact Philips about your Allura Xper FD10C system
Philips has identified that some Allura Xper FD10C X-ray systems may be missing a drip tray that sits beneath the cooling unit, or the installation was not properly documented during previous maintenance. Without this tray, coolant liquid could leak onto electrical components and cause short circuits, potentially shutting down the system.
- 2026-01-14FDA-DeviceClass IICheck your Philips MX40 patient monitor
Philips MX40 patient monitors may lose wireless connection to the PIC iX central station when moving between certain access points if the signal strength changes rapidly. This could interrupt patient data transmission to clinical staff.
- 2026-01-14FDA-DeviceClass IIStop using affected Philips Incisive CT scanners
Philips Healthcare has recalled certain Incisive CT scanners due to an unstable internal connection in the floating sensor. This instability may cause the scanner to produce incomplete or compromised scans. The issue affects 35 devices distributed across the U.S. and its territories, and no injuries have been reported.
- 2026-01-07FDA-DeviceClass IIStop using affected Philips EPIQ ultrasound systems
Philips EPIQ Ultrasound Systems with the X5-1c transducer and certain software versions may unexpectedly restart on their own. This automatic reboot can damage the transducer. No injuries have been reported.
- 2025-12-17FDA-DeviceClass IICheck your Philips Azurion 7 M20 X-ray system
Between July 2024 and June 2025, some Philips Azurion R3.0 fluoroscopic X-ray systems (model 722234) were shipped without a required safety spacer. This spacer ensures the X-ray tube maintains a safe distance from patients during standard fluoroscopy procedures, as required by FDA regulations.
- 2025-12-10FDA-DeviceClass IILumify Diagnostic Ultrasound System models : 795005, 795161, 989605449841,
Ultrasound system compatibility issues with Apple devices running iOS 18 may cause a failure to perform live imagining.
- 2025-12-10FDA-DeviceClass IICT 5300; Software Version Number: 4.5, 5.0, 5.1;
If the screws of tube heat exchanger on the rotating scanner are not tightened well after replacing. This component may become detached and make contact with other components located within the Incisive CT systems during rotation. Other components could be damaged due to the contact with the tube heat exchanger.
- 2025-12-10FDA-DeviceClass IIIncisive CT; Software Version Number: 4.5, 5.0, 5.1;
If the screws of tube heat exchanger on the rotating scanner are not tightened well after replacing. This component may become detached and make contact with other components located within the Incisive CT systems during rotation. Other components could be damaged due to the contact with the tube heat exchanger.
- 2025-12-10FDA-DeviceClass IIIntelliVue Patient Monitor MX850. Product Number: 866470.
Potential issue where the IntelliVue monitors did not alarm.
- 2025-12-10FDA-DeviceClass IIIntelliVue Patient Monitor MX800. Product Number: 865240.
Potential issue where the IntelliVue monitors did not alarm.
- 2025-12-10FDA-DeviceClass IIIntelliVue Patient Monitor MX750. Product Number: 866471.
Potential issue where the IntelliVue monitors did not alarm.
- 2025-12-10FDA-DeviceClass IIIntelliVue Patient Monitor MX700. Product Number: 865241.
Potential issue where the IntelliVue monitors did not alarm.
- 2025-12-10FDA-DeviceClass IIIntelliVue Patient Monitor MX600. Product Number: 865242.
Potential issue where the IntelliVue monitors did not alarm.
- 2025-12-10FDA-DeviceClass IIIntelliVue Patient Monitor MX550. Product Number: 866066.
Potential issue where the IntelliVue monitors did not alarm.
- 2025-12-10FDA-DeviceClass IIIntelliVue Patient Monitor MX500. Product Number: 866064.
Potential issue where the IntelliVue monitors did not alarm.
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