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Philips North America Llc

Philips North America Llc Recalls

All product recalls associated with Philips North America Llc.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

145

Most Recent

Jan 2026

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 201–220 of 37661 recalls

IntelliVue MP5 (Philips) – Alarm Failure Risk (2025)

Potential issue where the IntelliVue monitors did not alarm.

High

FDAOct 31, 2025Nationwide• Philips North America Llc

IntelliVue Patient Monitor MX700 (Philips) – Alarm Failure Risk (2025)

Potential issue where the IntelliVue monitors did not alarm.

High

FDAOct 31, 2025Nationwide• Philips North America Llc

IntelliVue MP40 (Philips) – monitoring alarm issue (2025)

Potential issue where the IntelliVue monitors did not alarm.

High

FDAOct 31, 2025Nationwide• Philips North America Llc

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IntelliVue MP70 (Philips) – Alarm Failure Risk (2025)

Potential issue where the IntelliVue monitors did not alarm.

High

FDAOct 31, 2025Nationwide• Philips North America Llc

IntelliVue MP30 (Philips) – monitoring alarm issue (2025)

Potential issue where the IntelliVue monitors did not alarm.

High

FDAOct 31, 2025Nationwide• Philips North America Llc

IntelliVue MP60 (Philips) – monitoring alarm issue (2025)

Potential issue where the IntelliVue monitors did not alarm.

High

FDAOct 31, 2025Nationwide• Philips North America Llc

IntelliVue MP90 (Philips) – Alarm Failure Risk (2025)

Potential issue where the IntelliVue monitors did not alarm.

High

FDAOct 31, 2025Nationwide• Philips North America Llc

IntelliVue Multi-Measurement Module X3 (Philips) – monitoring alarm issue (2025)

Potential issue where the IntelliVue monitors did not alarm.

High

FDAOct 31, 2025Nationwide• Philips North America Llc

IntelliVue MP20 (Philips) – Alarm Failure Risk (2025)

Potential issue where the IntelliVue monitors did not alarm.

High

FDAOct 31, 2025Nationwide• Philips North America Llc

Marinara Sauce (First & Last Tavern) – Botulinum Risk (2025)

May be contaminated with Clostridium botulinum

Class IIModerate

FDAOct 31, 2025CT, MA• First & Last Tavern

Phytonadione Injectable Emulsion (Cipla) – stability failure (2025)

Failed Stability Specifications: Observed OOS results: eg results for colour index

Class IIModerate

FDAOct 31, 2025Nationwide• Cipla Limited

Puttanesca Sauce (First & Last Tavern) – Botulinum Risk (2025)

May be contaminated with Clostridium botulinum

Class IIModerate

FDAOct 31, 2025CT, MA• First & Last Tavern

IntelliVue MP50 (Philips) – Alarm Failure Risk (2025)

Potential issue where the IntelliVue monitors did not alarm.

High

FDAOct 31, 2025Nationwide• Philips North America Llc

Traditional Pasta Sauce (First & Last Tavern) – Botulinum Risk (2025)

May be contaminated with Clostridium botulinum

Class IIModerate

FDAOct 31, 2025CT, MA• First & Last Tavern

NICO Myriad Handpiece (Stryker) – Latex Contamination Risk (2025)

Tape used to secure components within packaging contains latex, despite products being labeled as latex-free. Latex could potentially cause an allergic reaction.

Moderate

FDAOct 31, 2025Nationwide• Stryker Corporation

Stryker Arise 1000EX Mattress (Stryker) – Proximity Concern (2025)

Stryker has issued a voluntary recall of certain MV3 beds and Arise 1000EX mattresses because some of these products have been sold in close proximity, suggesting a potential intent for them to be used together. These products have not been tested for compatibility and thus are not designed to be used together. The combination of both is not recommended by Stryker.

Moderate

FDAOct 31, 2025Nationwide• Stryker Medical Division of Stryker Corporation

Stealth and Covert Kayak Paddles (Werner) – Drowning Risk (2025)

This recall involves models Stealth and Covert kayak paddles. The brand name Werner appears on decals on both blades and the model name is printed on the right paddle blade. The paddles are made of black carbon fiber.

High

CPSCOct 30, 2025Nationwide• Werner Paddles, of Tennessee

FlexLab FLX-217-10 (Inpeco) – Labeling Mismatch Risk (2025)

The Aliquoter Module (mALX) may generate secondary sample tubes without labels or with mismatched labels which may result in delayed results or erroneous results. This error occurs if the operators open the printer head of mALX to perform error recoveries or maintenance procedures and do not empty the printer tubes buffer to remove all the secondary sample tubes.

Moderate

FDAOct 30, 2025MI• Inpeco S.A. Via San Gottardo 10 Lugano Switzerland

FlexLab FLX-217-40 (Inpeco) – Labeling Mismatch Risk (2025)

The Aliquoter Module (mALX) may generate secondary sample tubes without labels or with mismatched labels which may result in delayed results or erroneous results, this error occurs if the operators open the printer head of mALX to perform error recoveries or maintenance procedures and do not empty the printer tubes buffer to remove all the secondary sample tubes

Moderate

FDAOct 30, 2025MI• Inpeco S.A. Via San Gottardo 10 Lugano Switzerland

Entegra Cornerstone Reserve (Entegra) – RV Slide Issue (2025)

Jayco, Inc. (Jayco) is recalling certain 2026 Entegra Cornerstone Reserve, 2025-2026 Cornerstone, Aspire, and Anthem recreational vehicles. The slide-out room can be deployed without the parking brake engaged, allowing the room to extend while the vehicle is in motion.

High

NHTSAOct 30, 2025Nationwide• ENTEGRA