GE Medical Systems recalls

18 recent recalls on record for GE Medical Systems in connected official government data as of October 22, 2026 at 6:00 PM UTC.

Models with recalls

Allia IGS 3 Pulse angiographic X-ray system (1)Allia IGS 5 Pulse angiographic X-ray system (1)Allia IGS 7 Pulse angiographic X-ray system (1)Allia IGS Pulse angiographic X-ray system (1)Allia Moveo angiographic X-ray system (1)Giraffe OmniBed (1)Giraffe OmniBed Carestations and Giraffe OmniBed Carestation CS1 (1)Giraffe OmniBed Field Replaceable Unit (FRU) (1)Optima XR200amx (1)Optima XR220amx (1)Optima XR240amx (1)Revolution Apex (1)Revolution Apex Elite (1)Revolution Apex Plus (1)Revolution Apex Select (1)Revolution Ascend (1)Revolution CT (1)Revolution CT ES (1)

All GE Medical Systems recalls

FDA Class II · Medical device · July 22, 2026

Optima XR240amx recall — GE Medical Systems, LLC

GE HealthCare has become aware that in certain Optima XR200/220/240amx systems that have had a column replacement completed, functional testing of the safety pawl may not have been…

Official ID Z-2728-2026 · Official record ↗

FDA Class II · Medical device · July 22, 2026

Optima XR220amx recall — GE Medical Systems, LLC

GE HealthCare has become aware that in certain Optima XR200/220/240amx systems that have had a column replacement completed, functional testing of the safety pawl may not have been…

Official ID Z-2727-2026 · Official record ↗

FDA Class II · Medical device · July 22, 2026

Optima XR200amx recall — GE Medical Systems, LLC

GE HealthCare has become aware that in certain Optima XR200/220/240amx systems that have had a column replacement completed, functional testing of the safety pawl may not have been…

Official ID Z-2726-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Giraffe OmniBed Field Replaceable Unit (FRU) recall — GE Medical Systems, LLC

GE HealthCare has become aware of a potential issue involving the canopy soffit beneath the control panel end of the device. Under certain conditions, for example, impact during tr…

Official ID Z-2477-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Giraffe OmniBed Carestations and Giraffe OmniBed Carestation CS1 recall — GE Medical Systems, LLC

GE HealthCare has become aware of a potential issue involving the canopy soffit beneath the control panel end of the device. Under certain conditions, for example, impact during tr…

Official ID Z-2476-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Giraffe OmniBed recall — GE Medical Systems, LLC

GE HealthCare has become aware of a potential issue involving the canopy soffit beneath the control panel end of the device. Under certain conditions, for example, impact during tr…

Official ID Z-2475-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Allia Moveo angiographic X-ray system recall — GE Medical Systems, LLC

GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead to a risk of electrica…

Official ID Z-2318-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Allia IGS Pulse angiographic X-ray system recall — GE Medical Systems, LLC

GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead to a risk of electrica…

Official ID Z-2317-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Allia IGS 7 Pulse angiographic X-ray system recall — GE Medical Systems, LLC

GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead to a risk of electrica…

Official ID Z-2316-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Allia IGS 5 Pulse angiographic X-ray system recall — GE Medical Systems, LLC

GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead to a risk of electrica…

Official ID Z-2315-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Allia IGS 3 Pulse angiographic X-ray system recall — GE Medical Systems, LLC

GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead to a risk of electrica…

Official ID Z-2314-2026 · Official record ↗

FDA Class II · Medical device · May 20, 2026