Philips North America recalls
112 recalls filed under Philips North America. The most recent was published February 4, 2026.
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Class II · 9 months ago
Philips North America SmartPath to dStream for 3.0T. Product Code : 782145. MR systems recall: The potential for stiffness value errors when viewing exported MR
The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication…
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Class II · 9 months ago
Philips North America Patient Information Center iX recall: A recent software (SW) patch modifies Mobile Event Notification filter
A recent software (SW) patch modifies Mobile Event Notification filter settings without providing any indication to the user when upgrading the…
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Class II · 9 months ago
Philips Smart-hopping 2.0 AP 1.4 GHz. Patient Monitor recall: It was found that the MX40 device could not reconnect to the PIC iX
It was found that the MX40 device could not reconnect to the PIC iX when moving between Radiohead and Trident 1.4 GHz access points if the signal…
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Class II · 10 months ago
Philips North America Azurion R3.0 recall: Between July 2024 and June 2025, Philips Azurion R3.0 systems with a FlexArm
Between July 2024 and June 2025, Philips Azurion R3.0 systems with a FlexArm stand were shipped without the Source-to-Skin Distance (SSD) Spacer. The…
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Class II · 11 months ago
Philips North America Llc IntelliVue MP70. Product Number: M8007A recall: Potential issue where the IntelliVue monitors did not alarm
Potential issue where the IntelliVue monitors did not alarm.
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Class II · 11 months ago
Philips North America Llc IntelliVue Patient Monitor MX450. Product Number: 866062 recall: Potential issue where the IntelliVue monitors did not alarm
Potential issue where the IntelliVue monitors did not alarm.
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Class II · 11 months ago
Philips North America Llc IntelliVue Patient Monitor MX750. Product Number: 866471 recall: Potential issue where the IntelliVue monitors did not alarm
Potential issue where the IntelliVue monitors did not alarm.
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Class II · 11 months ago
Philips North America Llc IntelliVue Patient Monitor MX550. Product Number: 866066 recall: Potential issue where the IntelliVue monitors did not alarm
Potential issue where the IntelliVue monitors did not alarm.
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Class II · 11 months ago
Philips North America Llc IntelliVue Multi-Measurement Module X3. Product Number recall: Potential issue where the IntelliVue monitors did not alarm
Potential issue where the IntelliVue monitors did not alarm.
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Class II · 11 months ago
Philips North America Llc IntelliVue Patient Monitor MX400. Product Number: 866060 recall: Potential issue where the IntelliVue monitors did not alarm
Potential issue where the IntelliVue monitors did not alarm.
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Class II · 11 months ago
Philips North America Llc IntelliVue Patient Monitor MX600. Product Number: 865242 recall: Potential issue where the IntelliVue monitors did not alarm
Potential issue where the IntelliVue monitors did not alarm.
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Class II · 11 months ago
Philips North America Llc IntelliVue MP20. Product Number: M8001A recall: Potential issue where the IntelliVue monitors did not alarm
Potential issue where the IntelliVue monitors did not alarm.
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Class II · 11 months ago
Philips North America Llc IntelliVue MP5. Product Number: M8105A recall: Potential issue where the IntelliVue monitors did not alarm
Potential issue where the IntelliVue monitors did not alarm.
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Class II · 11 months ago
Philips North America Llc IntelliVue MP60. Product Number: M8005A recall: Potential issue where the IntelliVue monitors did not alarm
Potential issue where the IntelliVue monitors did not alarm.
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Class II · 11 months ago
Philips North America Llc IntelliVue Multi Measurement Server X2. Product Number recall: Potential issue where the IntelliVue monitors did not alarm
Potential issue where the IntelliVue monitors did not alarm.
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Class II · 11 months ago
Philips North America Llc IntelliVue MP40. Product Number: M8003A recall: Potential issue where the IntelliVue monitors did not alarm
Potential issue where the IntelliVue monitors did not alarm.
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Class II · 11 months ago
Philips North America Llc IntelliVue Patient Monitor MX100. Product Number: 867033 recall: Potential issue where the IntelliVue monitors did not alarm
Potential issue where the IntelliVue monitors did not alarm.
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Class II · 11 months ago
Philips North America Llc IntelliVue MP80. Product Number: M8008A recall: Potential issue where the IntelliVue monitors did not alarm
Potential issue where the IntelliVue monitors did not alarm.
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Class II · 11 months ago
Philips North America Llc IntelliVue MP50. Product Number: M8004A recall: Potential issue where the IntelliVue monitors did not alarm
Potential issue where the IntelliVue monitors did not alarm.
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Class II · 11 months ago
Philips North America Llc Incisive CT recall: If the screws of tube heat exchanger on the rotating scanner
If the screws of tube heat exchanger on the rotating scanner are not tightened well after replacing. This component may become detached and make…
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Class II · 11 months ago
Philips North America Llc IntelliVue MP2. Product Number: M8102A recall: Potential issue where the IntelliVue monitors did not alarm
Potential issue where the IntelliVue monitors did not alarm.
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Class II · 11 months ago
Philips North America Llc IntelliVue Patient Monitor MX850. Product Number: 866470 recall: Potential issue where the IntelliVue monitors did not alarm
Potential issue where the IntelliVue monitors did not alarm.
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Class II · 11 months ago
Philips North America Llc IntelliVue Patient Monitor MX500. Product Number: 866064 recall: Potential issue where the IntelliVue monitors did not alarm
Potential issue where the IntelliVue monitors did not alarm.
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Class II · 11 months ago
Philips North America Llc CT 5300 recall: If the screws of tube heat exchanger on the rotating scanner
If the screws of tube heat exchanger on the rotating scanner are not tightened well after replacing. This component may become detached and make…
About this page
Philips North America appears here because a federal agency named it as the recalling firm or the brand on the label. A recall is not a judgement about everything the company sells — it covers only the lot codes and models listed in each notice.