Ge Medical Systems recalls

Ge Medical Systems appears in 168 official U.S. recall notices indexed by RecallRadar.

Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.

• GE Optima MR450w 1.5T, Nuclear Magnetic Resonance Imaging System
  FDA Device · Class II · 2025-08-20 · Ge Medical Systems
• SIGNA Architect AIR
  FDA Device · Class II · 2025-07-30 · Ge Medical Systems
• SIGNA PET/MR
  FDA Device · Class II · 2025-07-30 · Ge Medical Systems
• SIGNA Architect
  FDA Device · Class II · 2025-07-30 · Ge Medical Systems
• Discovery MR750w 3.0T
  FDA Device · Class II · 2025-07-30 · Ge Medical Systems
• OEC 3D
  FDA Device · Class II · 2025-06-18 · Ge Medical Systems
• OEC Elite: The OEC Elite mobile C-arm is intended to provide fluoroscopic and digital spot images of the patient anatomy, interventional to…
  FDA Device · Class II · 2025-06-18 · Ge Medical Systems
• Venue Go Models: R2 (Model Number H45181VG), R3 (Model Number H45193VG), R4 (Model Number H45114VG), R5 (Model Numbers H45135VG, H45135VGW)…
  FDA Device · Class II · 2025-04-23 · Ge Medical Systems
• Venue Fit Models: R3 (Model Number H45303VFSC, H45303VFSW), R4 (Model Number H45314VFS, H45314VFSW), Venue Fit R5 system (Model Numbers H45…
  FDA Device · Class II · 2025-04-23 · Ge Medical Systems
• GE Healthcare Revolution Apex Select, System, X-ray, Tomography, Computed
  FDA Device · Class II · 2025-03-19 · Ge Medical Systems
• GE Healthcare Revolution CT ES, System, X-ray, Tomography, Computed
  FDA Device · Class II · 2025-03-19 · Ge Medical Systems
• GE Healthcare Revolution Apex Expert, System, X-ray, Tomography, Computed
  FDA Device · Class II · 2025-03-19 · Ge Medical Systems
• GE Healthcare Revolution Apex Plus, System, X-ray, Tomography, Computed
  FDA Device · Class II · 2025-03-19 · Ge Medical Systems
• GE Healthcare Revolution CT, System, X-ray, Tomography, Computed
  FDA Device · Class II · 2025-03-19 · Ge Medical Systems
• GE Healthcare Revolution Apex, System, X-ray, Tomography, Computed
  FDA Device · Class II · 2025-03-19 · Ge Medical Systems
• GE Healthcare Revolution Apex Elite, System, X-ray, Tomography, Computed
  FDA Device · Class II · 2025-03-19 · Ge Medical Systems
• Definium 656HD & Discovery XR656HD (GTINs: 00840682138598, 00195278840226, 00840682136709)
  FDA Device · Class II · 2025-02-12 · Ge Medical Systems
• Discovery XR656HD. X-Ray imaging system
  FDA Device · Class II · 2025-02-12 · Ge Medical Systems
• Discovery XR656 HD. X-Ray imaging system
  FDA Device · Class II · 2025-02-12 · Ge Medical Systems
• Optima XR646 HD. X-Ray imaging system
  FDA Device · Class II · 2025-02-12 · Ge Medical Systems
• Portrait Core Services, a set of software services that enable the communication and interaction of the Portrait Mobile Monitoring Solution…
  FDA Device · Class II · 2025-01-22 · Ge Medical Systems
• GE Healthcare Optima XR200amx, Mobile Digital Radiographic System, Model Numbers: 1) 5555000-3
  FDA Device · Class II · 2025-01-15 · Ge Medical Systems
• GE Healthcare Optima XR240amx, Mobile Digital Radiographic System, Model Numbers: 1) 5555000-27
  FDA Device · Class II · 2025-01-15 · Ge Medical Systems
• Tec 6 Plus Anesthesia Vaporizer, Reference Numbers 1107-9601-000, 1107-9602-000, 1107-9603-000, 1107-9604-000, 1107-9610-000, 1107-9612-000…
  FDA Device · Class II · 2025-01-15 · Ge Medical Systems
• Tec 850 ISO Anesthesia Vaporizer, Reference Number 1177-9850-ISO
  FDA Device · Class II · 2025-01-15 · Ge Medical Systems
• Tec 820 SEV Anesthesia Vaporizer, Reference Number 1177-9820-SEV
  FDA Device · Class II · 2025-01-15 · Ge Medical Systems
• Tec 820 ISO Anesthesia Vaporizer, Reference Number 1177-9820-ISO
  FDA Device · Class II · 2025-01-15 · Ge Medical Systems
• GE Healthcare Optima XR220amx, Mobile Digital Radiographic System, Model Numbers: 1) 5555000-12
  FDA Device · Class II · 2025-01-15 · Ge Medical Systems
• Tec 850 SEV Anesthesia Vaporizer, Reference Number 1177-9850-SEV
  FDA Device · Class II · 2025-01-15 · Ge Medical Systems
• Tomographic Imager Combining Emission Computed Tomography With Nuclear Magnetic Resonance: 1) SIGNA PET/MR, 2) DISCOVERY PET/MR
  FDA Device · Class II · 2024-12-04 · Ge Medical Systems
• SIGNA Architect, Nuclear Magnetic Resonance Imaging System
  FDA Device · Class II · 2024-12-04 · Ge Medical Systems
• SIGNA Architect AIR, Nuclear Magnetic Resonance Imaging System
  FDA Device · Class II · 2024-12-04 · Ge Medical Systems
• Discovery MR750w 3.0T, whole body magnetic resonance scanner
  FDA Device · Class II · 2024-12-04 · Ge Medical Systems
• SIGNA Prime, with affected software versions: MR30.1
  FDA Device · Class II · 2024-08-14 · Ge Medical Systems
• SIGNA 7.0T, with affected software versions: 7T29.1, MR30.1
  FDA Device · Class II · 2024-08-14 · Ge Medical Systems
• Optima MR450w 1.5T, with affected software versions: DV24.0, DV25.0, DV25.1, DV26.0, DV29.1, MR30.0, MR30.1
  FDA Device · Class II · 2024-08-14 · Ge Medical Systems
• SIGNA MR355, with affected software versions: SV25.5, SV25.6
  FDA Device · Class II · 2024-08-14 · Ge Medical Systems
• Discovery MR750w 3.0T, with affected software versions: DV24.0, DV25.0, DV25.1, DV26.0 to DV26.5, DV29.1, MR30.0, MR30.1
  FDA Device · Class II · 2024-08-14 · Ge Medical Systems
• SIGNA Architect, with affected software versions: DV26.0 to DV26.3, DV27.0 to DV27.3, DV28.0 to DV28.5, DV29.0, DV29.1, DV29.2, MR30.0, MR3…
  FDA Device · Class II · 2024-08-14 · Ge Medical Systems
• SIGNA Victor, with affected software versions: MR30.1
  FDA Device · Class II · 2024-08-14 · Ge Medical Systems
• Brivo MR355, with affected software versions: SV20.3, SV23.3, MR30.0, MR30.1
  FDA Device · Class II · 2024-08-14 · Ge Medical Systems
• SIGNA Pioneer, with affected software versions: PX25.0 to PX25.5, PX26.0, PX26.1, PX28.0 to PX28.4, PX29.0, PX29.1, MR30.0, MR30.1
  FDA Device · Class II · 2024-08-14 · Ge Medical Systems
• 1.5T SIGNA HDxt Family, with affected software versions: HD16.0_V03 to HD16.4, HD23.0_V03, HD28.0, HD29.1, MR30.0, MR30.1
  FDA Device · Class II · 2024-08-14 · Ge Medical Systems
• SIGNA Hero, with affected software versions: PX29.1, MR30.0, MR30.1
  FDA Device · Class II · 2024-08-14 · Ge Medical Systems
• 3.0T SIGNA HDxt Family, with affected software versions: RX27.0 to RX27.3, RX28.0, RX29.0 to RX29.2, MR30.0, MR30.1HD16.0_V03, HD23.0_V03
  FDA Device · Class II · 2024-08-14 · Ge Medical Systems
• SIGNA Premier, with affected software versions: RX27.0 to RX27.3, RX28.0, RX29.0 to RX29.2, MR30.0, MR30.1
  FDA Device · Class II · 2024-08-14 · Ge Medical Systems
• SIGNA PET/MR, with affected software versions: MP24.0, MP26.0, MP26.1, MR30.0, MR30.1
  FDA Device · Class II · 2024-08-14 · Ge Medical Systems
• SIGNA Explorer, with affected software versions: SV25.5, SV25.6, SV29.2, MR30.0, MR30.1
  FDA Device · Class II · 2024-08-14 · Ge Medical Systems
• SIGNA MAGNUS, with affected software versions: MR29.1, RX29.1
  FDA Device · Class II · 2024-08-14 · Ge Medical Systems
• Optima MR360, with affected software versions: SV20.3, SV23.3, MR30.0, MR30.1
  FDA Device · Class II · 2024-08-14 · Ge Medical Systems