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 4, 2026

Philips Ingenia Ambition X recall — FDA Z-1210-2026

The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS).

Class IIFDA: OngoingPhilips North America
Medical DeviceFeb 4, 2026

Philips Upgrade to MR 7700 recall — FDA Z-1214-2026

The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS).

Class IIFDA: 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.