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OEC Medical Systems, Inc

OEC Medical Systems, Inc Recalls

All product recalls associated with OEC Medical Systems, Inc.

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Recall Summary

Total Recalls

1000

Past Year

893

Class I (Serious)

124

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 15301–15320 of 17593 recalls

OEC Medical Systems, Inc: GE OEC 9900 Elite ESP fluoroscopic x-ray system. GE Healt...

Under certain conditions, x-ray system may experience operational impairment.

FDAAug 29, 2008Nationwide• OEC Medical Systems, Inc

OEC Medical Systems, Inc: GE OEC 9900 Elite GSP fluoroscopic x-ray system GE Health...

Under certain conditions, x-ray system may experience operational impairment.

FDAAug 29, 2008Nationwide• OEC Medical Systems, Inc

Medtronic Inc. Cardiac Rhythm Managment: Medtronic Attain LDS 6216A, Left-heart delivery system. ...

Medtronic has identified an issue with the packaging for specific lots of the Medtronic Adjustable Valve and valves contained in the Attain Left Heart Delivery System kits. A small number of valve package seals could be compromised.

FDA

1...764 765766767 768...880

Page 766 of 880Next

Aug 27, 2008

GA, OR, RI +3 more

• Medtronic Inc. Cardiac Rhythm Managment

Medtronic Inc. Cardiac Rhythm Managment: Medtronic Attain ACCESS 6218A, Left-heart delivery syste...

FDAAug 27, 2008GA, OR, RI +3 more• Medtronic Inc. Cardiac Rhythm Managment

PTAC Air Conditioner Units (Goodman) – Fire Hazard (2008)

Fire/Burn Risk

The recall includes 5.0 kW Amana-brand, Comfort-Aire-brand and Century-brand PTAC units with model numbers PTxxx3x50xx (Amana) and EKTxxx-150x (Comfort-Aire and Century), and serial numbers 0702112056 through 0804237539. The model and serial numbers are located on the control board plate found under the PTAC unit's front cover.

CPSCAug 27, 2008Nationwide• Goodman Company L.P., of Houston, Texas

Medtronic Inc. Cardiac Rhythm Managment: Medtronic Adjustable Valve, 6248VAL, Sterilized using irr...

FDAAug 27, 2008GA, OR, RI +3 more• Medtronic Inc. Cardiac Rhythm Managment

Medtronic Neuromodulation: Medtronic SynchroMed EL Programmable Pump, Model 8626-10....

Medtronic issued a letter to healthcare professionals providing important safety information regarding MRI (magnetic resonance imaging) effects on SynchroMed EL and SynchroMed II implantable infusion pumps. As stated in product labeling, the magnetic field of an MRI will temporarily stop the rotor of the pump motor and suspend drug infusion for the duration of MRI exposure for all SynchroMed pump

FDAAug 25, 2008WA, PR• Medtronic Neuromodulation

Medtronic Neuromodulation: Medtronic SynchroMed II Programmable Pump, Model 8637-20....

FDAAug 25, 2008WA, PR• Medtronic Neuromodulation

Acumed LLC: Intramedullary Fixation Rod, common name Fibula Rod, labe...

Products improperly handled after cleaning, prior to sanitation and may be contaminated with inorganic material.

FDAAug 21, 2008CA, IN, MA +2 more• Acumed LLC

Philips Medical Systems North America Co. Phillips: Allura Xper FD10 Monoplane X-ray system. Intended for use...

Due to a potential geometry software lock up during a Digital Rotational Angiography (DRA) run, the stand and table movement may no longer be possible.

FDAAug 21, 2008Nationwide• Philips Medical Systems North America Co. Phillips

Philips Medical Systems North America Co. Phillips: Allura Xper FD10/10 Biplane X-ray system. Intended for us...

Potential for table and stand not to move due to a software error.

FDAAug 21, 2008Nationwide• Philips Medical Systems North America Co. Phillips

Wolf SL Carbon Bicycle Forks (True Temper) – Fall Hazard (2008)

The recalled forks have a clear coating over black painted carbon fiber, with the words "Wolf Superlite" and related logo just below the crown on each fork leg, and the letters "SL" on each leg above the fork blade dropouts. There is a True Temper CRT™ logo on the inside of both fork legs. The recalled forks could have been included on the following bicycle models: R3, R3 SL, Soloist Carbon, Soloist Carbon SL, and certain P3 Carbon framesets and complete bicycles.

CPSCAug 20, 2008Nationwide• True Temper Composite Material Products Co. Ltd, of Guangzhou, China

GE Medical Systems, LLC: Sterile, Drape, Headset, Upper, Part Number 888945-01.

GE Healthcare has found that the sterile products manufactured by Contour Fabricators, Inc. (CFI) for GE healthcare (GEHC) may have seals that could be compromised during the shelf life of the products. This issue could result in the product not maintaining its sterile state. Eleven complaints and 3 MDR's have been filed. No illness or injuries reported.

FDAAug 15, 2008Nationwide• GE Medical Systems, LLC

GE Medical Systems, LLC: Disposable Pack, Headset Part Number 888946-01(kit includ...

FDAAug 15, 2008Nationwide• GE Medical Systems, LLC

Philips Medical Systems North America Co. Phillips: Essenta DR is a digital multifunctional X-ray systems, su...

When a patient is selected in the patient list and examination tab pressed with background query running at the same time, the wrong patient may be selected.

FDAAug 15, 2008Nationwide• Philips Medical Systems North America Co. Phillips

GE Medical Systems, LLC: Sterile, Drape, Headset, Lower, Part Number 888944-01.

FDAAug 15, 2008Nationwide• GE Medical Systems, LLC

GE Medical Systems, LLC: GE Medical Systems, OEC, Vascular Drape, 00-902776-01, St...

FDAAug 15, 2008Nationwide• GE Medical Systems, LLC

Philips Medical Systems: Philips Diagnostic Ultrasound System, Model HD3. Product...

The system has a software defect that affects the display of Estimated Fetal Weight (EFW) Growth Percentile result values.

FDAAug 12, 2008PR• Philips Medical Systems

OEC Medical Systems, Inc: GE OEC 9900 Elite Fluoroscopic X-Ray System, GE Healthcar...

Beam limitation may be non-compliant on some X-ray units.

FDAAug 12, 2008Nationwide• OEC Medical Systems, Inc

OEC Medical Systems, Inc: GE OEC 9800 Fluoroscopic X-Ray System, GE Healthcare, Sur...

Beam limitation may be non-compliant on some X-ray units.

FDAAug 12, 2008Nationwide• OEC Medical Systems, Inc