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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

233

Past Year

Class I (Serious)

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 221–233 of 233 recalls

Philips North America LLC: Philips, HeartStart FR2 + Defibrillator, Model # M3860A a...

Customers were not notified of previous recalls associated with various defibrillator models.

Moderate

FDAFeb 9, 2021CA, CT, FL +9 more• Philips North America LLC

Philips North America LLC: Philips, HeartStart FRx + Defibrillator, Model # Model #s...

Customers were not notified of previous recalls associated with various defibrillator models.

Moderate

FDAFeb 9, 2021CA, CT, FL +9 more• Philips North America LLC

Philips North America LLC: Philips, HeartStart HS1 Home Defibrillator, Model # Model...

Customers were not notified of previous recalls associated with various defibrillator models.

Moderate

FDAFeb 9, 2021CA, CT, FL +9 more• Philips North America LLC

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Philips North America LLC: Philips, HeartStart HS1 OnSite Defibrillator, Model #'s: ...

Customers were not notified of previous recalls associated with various defibrillator models.

Moderate

FDAFeb 9, 2021CA, CT, FL +9 more• Philips North America LLC

Philips North America, LLC: IntelliVue G7m Anesthesia Gas Module, Model no. 866173, F...

The device may experience an interruption of gas measurement due to a firmware issue, ceasing measurement and display of gas levels and generating one or more technical or INOP alarms.

Moderate

FDAJun 25, 2020Nationwide• Philips North America, LLC