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GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc Recalls

All product recalls associated with GE OEC Medical Systems, Inc.

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Recall Summary

Total Recalls

1000

Past Year

353

Class I (Serious)

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 2881–2900 of 3680 recalls

GE OEC Medical Systems, Inc: GEHC OEC 8800 Mobile Fluoroscopic X-ray System, GE Health...

X-ray units did not meet manufacturer's specification for linearity.

Class IIModerate

FDAOct 19, 2007Nationwide• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: GE OEC, Insta Trak 3500 Plus with the Cranial Application...

Crack, Fracture or Detachment: The Transmitter Arm for the Mayfield-compatible Transmitter may become detached from the unit and enter into the surgical field.

FDAOct 18, 2007AL, AZ, AR +22 more• GE OEC Medical Systems, Inc

Aesculap Implant Systems: Excia Cemented Hip Stems, Size 9mm, Part Number: NJ309K, ...

Sterility (package integrity) Compromised: Device package damaged during shipment

FDA

1...143 144145146 147...184

Page 145 of 184Next

Oct 10, 2007

Nationwide

• Aesculap Implant Systems

Stelkast Co: StelKast Proven Knee System - Tibial Half Block Augmenta...

The screws may fracture

FDAOct 5, 2007Nationwide• Stelkast Co

Stelkast Co: StelKast Proven Knee - Tibial Half Block Augmentation and...

The screws may fracture

FDAOct 5, 2007Nationwide• Stelkast Co

Acist Medical Systems: ACIST Multi-Use Syringe Kit, Model A2000; SKU # : 014612;...

Syringe Fracture: the syringe may be fractured, causing contrast to be sprayed from syringe fracture.

FDAOct 3, 2007Nationwide• Acist Medical Systems

Rita Medical Systems, Inc.: Vortex VX, Port System, 9.6FR, REF/Part Number : P5455K, ...

Incorrect Size Catheter: The product may contain an incorrect size catheter.

FDAOct 3, 2007AL, AR, CA +8 more• Rita Medical Systems, Inc.

Varian Medical Systems Inc: Varian brand VARiS 1.4g (Medical Charged Particle Radiati...

Incorrect Software Validation- The ARC treatment plans containing a Dose Dynamic MLC for IMRT delivery that will not be recognized properly by the system. Under these circumstances, an arc plan can be administered to a patient whereby the gantry will not rotate, resulting in delivery to a single location rather than through the gantry arc.

FDAOct 2, 2007Nationwide• Varian Medical Systems Inc

Medtronic Perfusion Systems: Medtronic Trillium Affinity NT, 541T, Integrated CVR/Mem...

Unnaproved Component Resin: Affinity NT Integrated CVR Membrane Oxygenators and EL 240 Autotransfusion Blood Collection Reservoirs contain components made from an unapproved resin

FDAOct 1, 2007Nationwide• Medtronic Perfusion Systems

Medtronic Perfusion Systems: Medtronic Blood Collection Reservoir, 40 micron,Catalog/M...

Unnaproved Component Resin: Affinity NT Integrated CVR Membrane Oxygenators and EL 240 Autotransfusion Blood Collection Reservoirs contain components made from an unapproved resin

FDAOct 1, 2007Nationwide• Medtronic Perfusion Systems

Stryker Howmedica Osteonics Corp.: Hipstar V40 Femoral Stem-127 degrees; N degrees 3 high of...

Mis-labeling; The warning label "Do not use with heads more than +10mm offset" does not appear on 127 degree stem boxes.

FDASep 28, 2007Nationwide• Stryker Howmedica Osteonics Corp.

Stryker Howmedica Osteonics Corp.: Hipstar TMZF Cementless Hip Stem Protocol, Product Number...

Mis-labeling: An error on page 4 of the Hipstar protocol was found. In the table for compatible Heads, the 40 mm diameter heads with a Neck Length of +12 should have been omitted.

FDASep 28, 2007Nationwide• Stryker Howmedica Osteonics Corp.

GE OEC Medical Systems, Inc: GE Healthcare, Mobile Fluoroscopy X-Ray System, OEC Model...

Unnecessary operator exposure; X-ray machine may allow unwanted x-ray exposure to the operator.

FDASep 28, 2007CO, DE, FL +6 more• GE OEC Medical Systems, Inc

X-15 Flying Model Rockets (Estes-Cox) – Impact Injury Risk (2007)

This recall involves the X-15 flying model rocket, a 1:44 scale version of the North American Aviation hypersonic rocket plane. The model rockets are about 13.5 inches long and have a wingspan of about 5 inches. The rockets are black and yellow, and have the number 66670 on the tail. The rockets were sold individually (item #1890) and as part of a starter kit (item #1412). The item number is printed on the product's instruction sheet and above the bar code on the product's packaging.

CPSCSep 28, 2007Nationwide• Estes-Cox Corp., of Penrose, Colo.

Stryker Howmedica Osteonics Corp.: Hipstar V40 Femoral Stem-127 degrees; Catalog No: 7850-5-...

Mis-labeled: The warning label "Do not use with heads more than +10mm offset" does not appear on 127 degree stem boxes.

FDASep 28, 2007Nationwide• Stryker Howmedica Osteonics Corp.

Stryker Howmedica Osteonics Corp.: Stryker T2 Locking Screw, Fully threaded; 05 x 70mm, Cata...

Mislabeled: One lot of screws (05x70mm) is labeled as containing 70mm, but may actually contain 75mm length screws.

FDASep 27, 2007Nationwide• Stryker Howmedica Osteonics Corp.

Philips Medical Systems (Cleveland) Inc: The Brilliance CT Big Bore is a whole body computed tomog...

The maximum intensity projection (MIP) images produced from respiratory gated images by the Tumor Localization (Tumor LOC) software application on Brilliance Big Bore CT scanners will be labeled incorrectly for certain patient orientations and view conventions when saved for later viewing.

FDASep 27, 2007PR• Philips Medical Systems (Cleveland) Inc

Varian Medical Systems Inc: Varian Real-Time Position Management System (RPM), A Resp...

Erroneously Resetting: RPM System version 1.7.3, software failure can occur that affects the gated radiotherapy treatment when phase-based gating is used. RPM 1.7 erroneously resets the phase-based gating thresholds to system default during the treatment session, if the user accesses the Session options during the treatment session. This can lead to difference between the planned and delivered

FDASep 26, 2007Nationwide• Varian Medical Systems Inc

Philips Medical Systems North America Co. Phillips: Allura Xper FD20/10, Release 1.2, Philips Medical Systems...

Inaccurate anatomical measurements when using the optional SmartMask feature

FDASep 24, 2007Nationwide• Philips Medical Systems North America Co. Phillips

Philips Medical Systems North America Co. Phillips: Allura Xper FD20 X-Ray System, Release 2.2, Philips Medic...

Inaccurate anatomical measurements when using the optional SmartMask feature

FDASep 24, 2007Nationwide• Philips Medical Systems North America Co. Phillips