Recall company profile

Philips North America Recalls

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

123recall records
Sep 23, 2026latest record date
May 24, 2023earliest record date

Recall history in this database

Classification mix: Class II: 114, Class III: 6, Class I: 3.

Medical DeviceFeb 7, 2024

Philips Intera 1.5T Achieva Nova recall — FDA Z-0952-2024

The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the scanning process, the risk to…

Class IIFDA: OngoingPhilips North America
Medical DeviceFeb 7, 2024

Philips Achieva 1.5T Initial system recall — FDA Z-0947-2024

The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the scanning process, the risk to…

Class IIFDA: OngoingPhilips North America
Medical DeviceFeb 7, 2024

Philips Intera Achieva 1.5T Pulsar recall — FDA Z-0954-2024

The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the scanning process, the risk to…

Class IIFDA: OngoingPhilips North America
Medical DeviceFeb 7, 2024

Philips Achieva 1.5T Conversion recall — FDA Z-0946-2024

The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the scanning process, the risk to…

Class IIFDA: OngoingPhilips North America
Medical DeviceJan 31, 2024

Philips Achieva 3.0T, Model No. 781177 recall — FDA Z-0809-2024

An incorrect electrical shock warning label may have been placed on the Liquid Cooling Cabinet (LCC) of affected MR systems. The caution symbol on the incorrect label has a white background…

Class IIIFDA: OngoingPhilips North America
Medical DeviceJan 31, 2024

Philips Intera 1.5T, Model No. 781195 recall — FDA Z-0811-2024

An incorrect electrical shock warning label may have been placed on the Liquid Cooling Cabinet (LCC) of affected MR systems. The caution symbol on the incorrect label has a white background…

Class IIIFDA: OngoingPhilips North America

Understanding this recall history

This page summarizes recall records in which the official source identifies Philips North America 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.