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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

583

Class I (Serious)

Most Recent

Dec 2025

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 9981–10000 of 10937 recalls

GE OEC Medical Systems, Inc: GE OEC 9900 Elite Digital Mobile C-Arm X-ray system, GE O...

X-ray systems could provide output which exceeds the 20 R/minute limit.

FDAAug 16, 2006Nationwide• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: RUS Tool Version Software

X-ray systems could provide output which exceeds the 20 R/minute limit.

FDAAug 16, 2006Nationwide• GE OEC Medical Systems, Inc

Hitachi Medical Systems America Inc: MRP-7000 and AIRIS Magnetic Resonance Imaging Systems, So...

Image orientation error. When a 3D Maximum Intensity Projection (MIP) image data set is transferred from the MRI system to a computer workstation via the DICOM protocol, the anatomical markers do not change between the images as they rotate.

FDA

1...498 499500501 502...547

Page 500 of 547Next

Aug 16, 2006

Nationwide

• Hitachi Medical Systems America Inc

Hitachi Medical Systems America Inc: Hitachi Echelon Magnetic Resonance Imaging System, Serial...

Component defect/overheating device; A malfunctioning decoupling circuit in the CTL coil caused high current flow and circuit overheating.

FDAAug 14, 2006Nationwide• Hitachi Medical Systems America Inc

Respironics Novametrix, LLC.: NICO Model 7300 Cardiopulmonary Management System

Audible alarm may not sound during an alert condition

FDAAug 11, 2006PR• Respironics Novametrix, LLC.

Becton Dickinson & Company: BD Vacutainer Push Button Blood Collection Set with Pre-a...

A complaint was received regarding a BD blood collection set where the blister was noticeably warped. The seal width was below minimum specification. Some blisters could adhere together and crack upon separation. Some units may have pre-activated or have defects affecting package integrity.

FDAAug 11, 2006Nationwide• Becton Dickinson & Company

Michigan Instruments, Inc.: Michigan Instruments Thumper Mechanical CPR Device; Model...

Failure to initiate compressions when first turned on, if improperly shut down-Operator Manual updated to include proper shut down procedures

FDAAug 4, 2006Nationwide• Michigan Instruments, Inc.

CryoCath Technologies Inc. 16771 Chemin Ste-Marie Kirkland Canada: 7F Freezor Cardiac Cryoablation catheter, REF # 207F1. C...

Outer cartons of catheters were mislabeled with two different reference numbers. The front of the package showed the correct reference number; 207F1, however the section on the top of the box incorrectly referenced 207F3. All inside labels (inside the box and affixed on device pouches) showed the correct reference number, 207F1.

FDAAug 4, 2006Nationwide• CryoCath Technologies Inc. 16771 Chemin Ste-Marie Kirkland Canada

Medtronic Sofamor Danek Instrument Manufacturing: Implant Hollow Reamer, 14 mm, REF 8951405, Medtronic Sofa...

Laceration Risk

Bone reamer may not have a cutting surface on the tip.

FDAAug 1, 2006Nationwide• Medtronic Sofamor Danek Instrument Manufacturing

Becton Dickinson & Company: BD 1mL SafetyGlide Allergy and Tuberculin Syringes. Reor...

BD received reports of needle assembly disengagement from the syringe.

FDAJul 24, 2006Nationwide• Becton Dickinson & Company

Philips Medical Systems: IntelliVue MultiMeasurement Server (MMS)/Multimeasurement...

Patient monitor may display inaccurate reading when the Disposable Sp02 Sensor is not attached

FDAJul 24, 2006Nationwide• Philips Medical Systems

Microvision Medical Holding B.V. Meibergdreef 45 Amsterdam Netherlands: MicroScan Lens Disposable Plastic Cap used with MicroScan...

Some lenses may have microscopic holes in the disposable caps representing a potential break in the sterile barrier

FDAJul 21, 2006CA, IN, IA +4 more• Microvision Medical Holding B.V. Meibergdreef 45 Amsterdam Netherlands

Konica Minolta Medical Imaging USA, Inc.: Regius Model 370 Digital Radiography Konica Minolta

A hand grip column, even though locked in position, moved downward about 3 cm while a patient was holding the hand grip for lateral exposure. When the hand grip moved down, the patient who was holding it lost his or her balance and almost fell. This problem only occurred in Japan with one system.

FDAJul 14, 2006TX• Konica Minolta Medical Imaging USA, Inc.

Disetronic Medical Systems, Inc.: Disetronic D-TRONplus Insulin Pump Battery Pack; Ref/Cata...

The battery may turn the pump off without warning due to a design change in the battery.

FDAJul 13, 2006Nationwide• Disetronic Medical Systems, Inc.

Ryobi Radial Arm Saws (Ryobi) – Blade Detachment Risk (2006)

Laceration Risk

The recall involves all RA200 and RA202 radial arm saws. These are bench top models with 8¼-inch blades. Each unit has a data plate immediately behind the operator grip for the saw, which says "RYOBI 8 1/4" Radial Arm Saw" and either "RA200" or "RA202."

CPSCJul 13, 2006Nationwide• Ryobi Motor Products Corp. formerly of Anderson, S.C. ("RMP")

Lawn Tractors (Husqvarna) – Fire Hazard (2006)

Fire/Burn Risk

The lawn tractors were sold under the Husqvarna, Craftsman, Poulan Pro, Poulan, Weed Eater, Southern States and Murray brand names. Recalled tractors' product, model and serial numbers are listed in the chart below. To determine if a tractor is included in the recall, check the lawn tractors' product, model and serial numbers, located on a label under the seat of the tractor. Brand Product Number Model Number Serial Number Range Service Center Craftsman® NA 917.27662 917.27663 917.27618 917.27664 120905-X00XXXX through 061606-X00XXXX (800) 659-5917 Monday through Saturday between 6 a.m. and 8 p.m. ET. www.sears.com NA 917.27535 917.27639 917.27640 917.27641 917.27678 090905-X00XXXX through 062206-X00XXXX Husqvarna® 960430003 00 YT1942T 120905-X00XXXX through 061606-X00XXXX (866) 721-6091 Monday through Friday between 8 a.m. and 5 p.m. ET www.husqvarna.com 960130019 00 LT16542 090905-X00XXXX through 062206- X00X`XXX Murray 960120058 00 960120059 00 MB12538LT MB1842LT 120905-X00XXXX through 061606-X00XXXX (866) 284-8872 Monday through Friday between 8 a.m. and 5 p.m. ET Poulan® 960420026 00 C20H42YT 120905-X00XXXX through 061606-X00XXXX (866) 284-8872 Monday through Friday between 8 a.m. and 5 p.m. ET www.poulan.com 960120043 00 960120044 00 960120044 01 960120044 02 960120045 00 960120045 01 960120053 00 960170004 00 PO12538LT PB1638LT PB1638LT PB1638LT PB1842LT PB1842LT PB185H42LT PB18H42LT 090905-X00XXXX through 062206-X00XXXX Poulan Pro® 960420020 00 960420008 00 960420009 00 960420016 00 PB19H42YT PB20H42YT PK20H42YT XT19H42YT 120905-X00XXXX through 061606-X00XXXX (866) 284-8872 Monday through Friday between 8 a.m. and 5 p.m. ET www.poulan.com 960160013 00 960160013 01 960120060 00 HD17542 HD17542 XT185H42LT 090905-X00XXXX through 062206-X00XXXX Southern States 960420011 00 SO20H42YT 120905-X00XXXX through 061606-X00XXXX (866) 284-8872 Monday through Friday between 8 a.m. and 5 p.m. ET 960120054 00 960120055 00 960120057 01 SO1638LT SO17542LT SO19H42LT 090905-X00XXXX through 062206-X00XXXX Weed Eater® 960160014 00 960160014 02 HD13538 090905-X00XXXX through 062206-X00XXXX (866) 284-8872 Monday through Friday between 8 a.m. and 5 p.m. ET www.weedeater.com

CPSCJul 11, 2006Nationwide• Husqvarna Outdoor Products Inc., of Augusta, Ga., formerly known as Electrolux

Richard Wolf Medical Instruments Corp.: Tubing Set for TEM-Combined System; the tube set consists...

The irrigation tubing in the tube set was assembled incorrectly with the connectors reversed.

FDAJul 7, 2006Nationwide• Richard Wolf Medical Instruments Corp.

Lexar JumpDrive (Lexar) – Burn Hazard (2006)

Fire/Burn Risk

The recalled drives are high speed flash drives used to store, transfer and carry data from one computer to another. This recall only includes Lexar JumpDrive® FireFly which is sold in various colors, and Lexar JumpDrive® Secure II 1GB which has a metallic silver housing. "Lexar" is embossed on the front of the plastic housing and the capacity is marked on the back. The part number is located on the FireFly's packaging, and on the back of the Secure II 1GB drive. JumpDrive® FireFly Capacity Part Number 256MB (red) JDFF256-431RU JDFF256-264 JDFF256-445RU 512MB (lime green) JDFF512-431EM 1GB (blue) JDFF1GB-431TO 2GB (black) JDFF2GB-431BK JumpDrive® Secure II 1GB Part Number JDSE1GB-00-500 Rev H and 3052-1GBA-2006 JDSE1GB-00-500 Rev H and 3052-1GBA-2106 JDSE1GB-00-500 Rev H and 3052-1GBA-1906 JDSE1GB-00-500 Rev H and 3052-1GBA-1806

CPSCJul 6, 2006Nationwide• Lexar Media Inc., of Fremont, Calif.

Paloma Rattles (Tiffany) – Safety Hazard (2006)

Laceration Risk

The Paloma Rattle is a ring that is 2.5 inches in diameter. It consists of nine linked sterling-silver balls that contain small beads.

CPSCJul 5, 2006Nationwide• Cunill Orferbres, of Barcelona, Spain, for Tiffany and Company, of New York, N.Y.

Philips Medical Systems North America Co. Phillips: Easy Vision Workstation Family (for the manipulation and ...

Potential for measurements, lines, texts, etc to be stored incorrectly.

FDAJul 1, 2006Nationwide• Philips Medical Systems North America Co. Phillips