Skip to main content

Is My Product Recalled?

Food Recalls Medication Recalls Baby Products Pet Products Toys Electronics Household Vehicles Medical Devices Other

Scan How It Works Saved Get Alerts

Menu

Search All Recalls Latest Recalls Scan Barcode Get Alerts

Categories

Food Recalls Medication Recalls Baby Products Pet Products Toys Electronics Household Vehicles Medical Devices Other

Resources

How Recalls Work FAQ Recall Classifications Statistics & Trends About

Your Recalls

Loading...

Stay Informed

Get email alerts when new recalls match your interests.

Recall data is updated hourly from official government sources. Very recent recalls may not yet appear. About our data sources

About

We make U.S. recall data searchable and accessible for consumers and businesses.

Site

FAQ
Browse by State
Statistics
Recall Classifications
About
Enterprise API

Legal

Privacy Policy
Terms of Service
Report Incorrect Info

Official Sources

FDA Recalls ↗
USDA FSIS ↗
CPSC Recalls ↗
NHTSA Recalls ↗

Home
/
Brands
/
Philips North America Llc

Philips North America Llc Recalls

All product recalls associated with Philips North America Llc.

Get alerts for this brand

Recall Summary

Total Recalls

233

Past Year

46

Class I (Serious)

0

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 41–60 of 233 recalls

Veradius Unity (Philips) – Radiation Emission Risk (2025)

A wireless foot switch pedal may get stuck in the active position when the user releases the pedal, resulting in the emission of unintended radiation.

FDAFeb 25, 2025Nationwide• Philips North America Llc

Zenition 70 (Philips) – Radiation Emission Risk (2025)

A wireless foot switch pedal may get stuck in the active position when the user releases the pedal, resulting in the emission of unintended radiation.

FDAFeb 25, 2025Nationwide• Philips North America Llc

Zenition 50 (Philips) – Radiation Emission Risk (2025)

A wireless foot switch pedal may get stuck in the active position when the user releases the pedal, resulting in the emission of unintended radiation.

1 234 5...12

Page 3 of 12Next

Feb 25, 2025

Nationwide

• Philips North America Llc

IntelliVue Patient Monitor (Philips) – alarm failure (2025)

Potential failure to alarm for "No Device Data" INOP. The device to alarm after a Hamilton ventilator is disconnected from the EC10 Module or IntelliBridge I/O board.

FDAJan 15, 2025FL, NC• Philips North America Llc

IntelliBridge EC10 Module (Philips) – alarm failure (2025)

Potential failure to alarm for "No Device Data" INOP. The device to alarm after a Hamilton ventilator is disconnected from the EC10 Module or IntelliBridge I/O board.

FDAJan 15, 2025FL, NC• Philips North America Llc

IntelliVue Patient Monitor (Philips) – Alarm Failure (2025)

Potential failure to alarm for "No Device Data" INOP. The device to alarm after a Hamilton ventilator is disconnected from the EC10 Module or IntelliBridge I/O board.

FDAJan 15, 2025FL, NC• Philips North America Llc

Philips Smart-Hopping AP (Philips) – Channel Setting Problem (2024)

The following four issues are included: 1. Certain Channel Settings may result in an Access Point preventing a connected client device from roaming to another Access Point potentially causing the client device to appear to drop out from the network. 2. if the Access Point experiences a disconnection from the Access Point Controller exceeding 4 minutes, the Access Point may not transition through the desired state to all for clean reconnection of the client radio link. 3. Potential to experience higher than expected data dropouts, device disassociations/reassociations for their wireless clients, and frequent "Loss of AP" alerts. 4. Potential for the Smart-hopping Access Point is affected by a software issue where the Access Point will resent after 82.85 days when the frame counter reaches its limit. This causes the latest synchronization check to fail and potential for loss of patient data.

FDANov 20, 2024Nationwide• Philips North America Llc

Spectral CT Scanner (Philips) – Procedure Box Risk (2024)

Potential for a plan box not updated issue during Interventional procedure with Spectral CT that may lead to a collision with the operator or with the needle placed inside the patient, and an incorrect patient ID software issue that may lead to misdiagnosis.

FDANov 16, 2024Nationwide• Philips North America Llc

Mammotrak Diagnostic Coil 1.5T (Philips) – Patient Safety Risk (2024)

Potential safety issue where a patient may be harmed while preparing for or during a scan.

FDANov 4, 2024Nationwide• Philips North America Llc

dS Breast 7ch 3.0T (Philips) – Patient Safety Risk (2024)

Potential safety issue where a patient may be harmed while preparing for or during a scan.

FDANov 4, 2024Nationwide• Philips North America Llc

Mammotrak Interventional Coil (Philips) – Patient Safety Risk (2024)

Potential safety issue where a patient may be harmed while preparing for or during a scan.

FDANov 4, 2024Nationwide• Philips North America Llc

Mammotrak Diagnostic Coil 3.0T (Philips) – Patient Safety Risk (2024)

Potential safety issue where a patient may be harmed while preparing for or during a scan.

FDANov 4, 2024Nationwide• Philips North America Llc

dS Breast 7ch 1.5T (Philips) – Patient Safety Risk (2024)

Potential safety issue where a patient may be harmed while preparing for or during a scan.

FDANov 4, 2024Nationwide• Philips North America Llc

dS Breast 16ch 3.0T (Philips) – Patient Safety Risk (2024)

Potential safety issue where a patient may be harmed while preparing for or during a scan.

FDANov 4, 2024Nationwide• Philips North America Llc

Achieva TX Interventional Coil (Philips) – Patient Safety Risk (2024)

Potential safety issue where a patient may be harmed while preparing for or during a scan.

FDANov 4, 2024Nationwide• Philips North America Llc

ST SENSE Breast Dx Coil (Philips) – patient safety issue (2024)

Potential safety issue where a patient may be harmed while preparing for or during a scan.

FDANov 4, 2024Nationwide• Philips North America Llc

ST SENSE Breast Coil (Philips) – patient safety issue (2024)

Potential safety issue where a patient may be harmed while preparing for or during a scan.

FDANov 4, 2024Nationwide• Philips North America Llc

SENSE Breast Coil (Philips) – patient safety issue (2024)

Potential safety issue where a patient may be harmed while preparing for or during a scan.

FDANov 4, 2024Nationwide• Philips North America Llc

SENSE Breast Coil 3.0T 7ch (Philips) – patient safety issue (2024)

Potential safety issue where a patient may be harmed while preparing for or during a scan.

FDANov 4, 2024Nationwide• Philips North America Llc

dS Breast 16ch 1.5T (Philips) – Patient Safety Risk (2024)

Potential safety issue where a patient may be harmed while preparing for or during a scan.

FDANov 4, 2024Nationwide• Philips North America Llc