Recall company profile

Philips North America, LLC Recalls

Overview of recall records associated with Philips North America, LLC, including dates, categories and classifications where available.

375recall records
Sep 9, 2026latest record date
Dec 19, 2018earliest record date

Recall history in this database

Classification mix: Class II: 369, Class I: 4, Class III: 2.

Medical DeviceSep 9, 2026

Philips Brilliance recall — FDA Z-3040-2026

Philips has identified an unintended radiation issue with the Philips IQon, iCT, Ingenuity, and Brilliance CT 64 systems that could affect the performance of the equipment.

Class IIFDA: OngoingPhilips North America LLC
Medical DeviceFeb 18, 2026

Philips Spectral CT 7500 on Rails recall — FDA Z-1318-2026

As part of the CT systems sub assembly, thirty-two (32) fasteners are used to attach the rotor to the bearing within the gantry. One or more of these fasteners may not be torqued to…

Class IIFDA: OngoingPhilips North America LLC

Understanding this recall history

This page summarizes recall records in which the official source identifies Philips North America, LLC as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.