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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

896

Class I (Serious)

125

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 15721–15740 of 17592 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

Ladder Stands (Gorilla) – Fall Hazard (2007)

This recall involves Gorilla Kong Maxx Ladder Stands with model number 43032 and batch numbers G051507, G051507D, G061507D, G071507D, and G081507D. Model numbers are printed on the box only. Batch numbers are stamped on the vertical rail of the first ladder section. The stand is 19 feet to the shooting rail, or 16 feet 8 inches to the platform. The foot platform measures 17½ inches wide. This is the only Gorilla, Inc. ladder stand with these dimensions.

1...785 786787788 789...880

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CPSCOct 18, 2007Nationwide• Gorilla Inc., of Flushing, Mich.

Beckman Coulter Inc: Access Power Supply Assembly Sled Part Number: A48196/684...

Electrical grounding failure: During manufacturing, internal testing found one instrument wlth an intermittent failure of the electrical grounding. The source of the problem was traced to inadequate soldering.

FDAOct 17, 2007Nationwide• Beckman Coulter Inc

John Deere Gator Vehicles – Injury Risk (2007)

This recall involves the XUV and HPX Gator utility vehicles made by John Deere with model and serial numbers included below. These are four-wheeled vehicles with a cargo box. "John Deere", "Gator", "HPX" and "XUV" are printed on the side of the cargo box. The following model and serial numbers can be found on the serial number plate on the frame of the vehicle: Model Serial Number XUV 620i Gas MOXUVGX013294-016669 XUV 620i Gas MOXUVGT011480-012186 XUV 850D Diesel MOXUVDX011917-013329 XUV 850D Diesel MOXUVDT010001-010449 HPX 4X4 Diesel MOHP4DX050877-051453 HPX 4X4 Gas MOHP4GX051221-052763

CPSCOct 17, 2007Nationwide• Deere & Company, of Moline, Ill.

PML, Inc. dba Pml Microbiologicals Inc.: PML --IDS Rapid NH QC Set- Quality Control kit for cultur...

Incorrect micro-organism-- .Quality control In-vitro diagnostic test was manufactured with Cryptococcus neoformans (ATCC 76484) instead of Haemophilus parainfluenzae (ATCC 7901).

FDAOct 15, 2007Nationwide• PML, Inc. dba Pml Microbiologicals Inc.

Medtronic Inc. Cardiac Rhythm Managment: Medtronic Sprint Fidelis 6948 Steroid eluting, quadripola...

Medtronic Cardiac Rhythm Disease Management has voluntarily suspended worldwide distribution of the Sprint Fidelis family of defibrillation leads because of the potential for lead fractures. In addition, the company recommends against new implants of the leads (Sprint Fidelis Models: 6930, 6931, 6948, 6949). Medtronic, its Independent Physician Quality Panel, and Bruce Lindsay, M.D., Professor of

FDAOct 15, 2007PR• Medtronic Inc. Cardiac Rhythm Managment

Medtronic Inc. Cardiac Rhythm Managment: Medtronic Sprint Fidelis 6930 Steroid eluting, tripolar, ...

FDAOct 15, 2007PR• Medtronic Inc. Cardiac Rhythm Managment

Medtronic Inc. Cardiac Rhythm Managment: Medtronic Sprint Fidelis 6931 Steroid eluting, tripolar, ...

FDAOct 15, 2007PR• Medtronic Inc. Cardiac Rhythm Managment

PML, Inc. dba Pml Microbiologicals Inc.: PML -- LyfoCults Haemophilus parainfluenzae - micro organ...

Incorrect micro-organism-- Quality control In-vitro diagnostic test was manufactured with Cryptococcus neoformans (ATCC 76484) instead of Haemophilus parainfluenzae (ATCC 7901).

FDAOct 15, 2007Nationwide• PML, Inc. dba Pml Microbiologicals Inc.

Medtronic Inc. Cardiac Rhythm Managment: Medtronic Sprint Fidelis 6949 Steroid eluting, quadripola...

FDAOct 15, 2007PR• Medtronic Inc. Cardiac Rhythm Managment

PML, Inc. dba Pml Microbiologicals Inc.: PML -- Vitek NH ID Card (NHI) Set - Quality Control kit ...

Incorrect micro-organism-- .Quality control In-vitro diagnostic test was manufactured with Cryptococcus neoformans (ATCC 76484) instead of Haemophilus parainfluenzae (ATCC 7901).

FDAOct 15, 2007Nationwide• PML, Inc. dba Pml Microbiologicals Inc.

Gas Regulators (Fisher Controls) – Leak Hazard (2007)

Fire/Burn Risk

The recalled gas regulators were manufactured from March 2007 through May 2007 and installed on natural gas or LP-gas supply systems in homes and small commercial buildings. The recalls involves model HSR natural gas regulators and LP-gas regulators with model numbers 67CD, 67CH, 67CN, and 67CW, HSRL, R622, R622E, R622H, R632, R642, R652, R652E, R122H, R222, or R232. The model number can be found on a white label attached to the regulator spring case. The date of manufacture is also stamped on the regulator.

CPSCOct 12, 2007Nationwide• Fisher Controls International (FCI), of McKinney, Texas

Beckman Coulter Inc: Cytomics FC 500 Flow Cytometry System with CXP Software V...

Software error: This field action was initiated after Beckman Coulter determined that the CXP software does not refresh the dataset automatically under certain circumstances. The User documentation does not clearly state that the user should refresh the dataset after changes are made.

FDAOct 11, 2007Nationwide• Beckman Coulter Inc

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

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

FDAOct 10, 2007Nationwide• Aesculap Implant Systems

Beckman Coulter Inc: Beckman Coulter UniCel Dxl 800 Access Immunoassay System;...

Incorrect results: There is an increased variance in assay performance when the UniCel Dxl 800 Modification (MOD ID 10027) and/or UniCel Dxl 800 Modification (MOD ID 6733) have been implemented and there are room fluctuations after assay calibration between the extremes of the 18C and 32C operating range.

FDAOct 8, 2007Nationwide• Beckman Coulter Inc

SCC Soft Computer: Hospital Information System Results Reporting Interface V...

SCC Soft Computer, Clearwater, FL issued a Correction for Hospital Information System Results Reporting Interface Versions 4.0.2.38.1, 4.0.2.39.2, 4.0.2.40.1, and 4.0.2.41.1 on 10/05/2007. A software anomaly in the result reporting interface caused result comments entered after an empty line not to be sent to the HIS system. This included interpretative comments, results, and normal range c

FDAOct 5, 2007AL, CO, FL +14 more• SCC Soft Computer

Medtronic Image Guided Neurologics, Inc.: Nexframe Stereotactic System Kits, Model Number(s): DB-10...

Sterilty (package integrity) Compromised: Some failures were for damage to the outer pouch, while another set of failures were for the seals on this pouch. The seal between the inner tray and lid has not been compromised and the contents remain sterile, however, the sterility of the outer surfaces of the inner tray and lid cannot be assured.

FDAOct 4, 2007Nationwide• Medtronic Image Guided Neurologics, Inc.

Stryker Communications: Extron Electronics OEM, CAB, DVI-Male to DVI-Female Cable...

Intermitten or Complete Loss of Signal: out-of-specification DVI cables causing intermitten or complete loss of signal on monitors used in surgery.

FDAOct 3, 2007Nationwide• Stryker Communications

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