Recall company profile

GE Medical Systems, LLC Recalls

Overview of recall records associated with GE Medical Systems, LLC, including dates, categories and classifications where available.

125recall records
Jul 22, 2026latest record date
Aug 1, 2018earliest record date

Recall history in this database

Classification mix: Class II: 125.

Medical DeviceJul 30, 2025

GE Medical Systems SIGNA Architect recall — FDA Z-2130-2025

GE HealthCare has become aware that gradient coils for certain MR systems (see affected product list in this letter), under specific conditions, can produce elevated acoustic noise during…

Class IIFDA: OngoingGE Medical Systems, LLC
Medical DeviceJul 30, 2025

GE Medical Systems SIGNA PET/MR recall — FDA Z-2133-2025

GE HealthCare has become aware that gradient coils for certain MR systems (see affected product list in this letter), under specific conditions, can produce elevated acoustic noise during…

Class IIFDA: OngoingGE Medical Systems, LLC
Medical DeviceFeb 12, 2025

GE Medical Systems Discovery XR656 HD recall — FDA Z-1045-2025

The user can continue to take the next exposure after reaching the Automatic Exposure Control (AEC) limit, without taking any further actions to acknowledge or adjust exposure techniques.…

Class IIFDA: OngoingGE Medical Systems, LLC

Understanding this recall history

This page summarizes recall records in which the official source identifies GE Medical Systems, 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.