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Medtronic Neurological

Medtronic Neurological Recalls

All product recalls associated with Medtronic Neurological.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

143

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 34481–34500 of 37665 recalls

Medtronic Neurological: Medtronic Intrathecal Catheter, Model 8731, (part of infu...

Tip dislodgement during implantation-Medtronic is recalling Model 8731 Intrathecal Catheter and Model 8598 Intrathecal Catheter Distal Revision Kit because the platinum-iridium tip may be dislodged by the guide wire during implantation.

FDAJul 21, 2006Nationwide• Medtronic Neurological

Medline Industries Inc: Medline Strider Midi 3 Scooter; a three wheeled battery o...

The P&G Solo 60A electronic control unit on the Midi Scooters may overheat.

FDAJul 20, 2006Nationwide• Medline Industries Inc

Medline Industries Inc: Medline Strider Maxi 4 Scooter; a four wheeled battery op...

Under conditions of heavy use, signs of overheating of the main battery cables have been observed.

FDA

1...1723 172417251726 1727...1884

Page 1725 of 1884Next

Jul 20, 2006

Nationwide

• Medline Industries Inc

Medline Industries Inc: Medline Strider Midi 4 Scooter; a four wheeled battery op...

The P&G Solo 60A electronic control unit on the Midi Scooters may overheat.

FDAJul 20, 2006Nationwide• Medline Industries Inc

Medline Industries Inc: Medline Strider Maxi 3 Scooter; a three wheeled battery o...

Under conditions of heavy use, signs of overheating of the main battery cables have been observed.

FDAJul 20, 2006Nationwide• Medline Industries Inc

Medtronic Neurological: Medtronic Kinetra Dual Program Neurostimulator for Deep B...

A subset of Kinetra implantable neurostimulators may experience a failure of wire connections between the electronic hybrid circuit and battery which may lead to sudden cessation of therapy. Sudden cessation of therapy can result in the immediate return or worsening of underlying symptoms due to the progression of the disease state.

FDAJul 19, 2006PR• Medtronic Neurological

LYCKSELE Chair Bed (IKEA) – Fingertip Amputation Risk (2006)

Laceration Risk

This recall involves LYCKSELE chair beds and sofa beds produced before July 2005 and date stamped (year/week) 0526 and earlier. The frames are constructed of iron and have natural wood slats. IKEA, the article number (700-326-82 chair bed and 900-326-81 sofa bed) and a four-digit date stamp printed on a white sticker located on the underside of the product.

CPSCJul 19, 2006Nationwide• IKEA Home Furnishings, of Plymouth Meeting, Pa.

Monica and Turbo Hair Dryers (Style Tronics) – Electrocution Risk (2006)

Laceration Risk

The recall involves two models of pistol-type hair dryers: The Monica hair dryer has its model name and number, SW-117, written on the handle. It is made of black plastic and chrome, and the handle folds up. The Turbo 1200 model has model number DS-507 written on the back of the handle. The model name is written on the blower nozzle. They are green and white and green.

CPSCJul 19, 2006Nationwide• Style Tronics Inc., of Vernon, Calif.

Therakos Inc: Therakos Photopheresis Procedural Kit for use with the UV...

Centrifuge Bowl may leak

FDAJul 18, 2006Nationwide• Therakos Inc

Plus Orthopedics USA: UC-PLUS Solution Unicondylar Knee System, Model Numbers:...

The modified devices were distributed by Plus Orthopedics USA (Plus USA) June 10, 2003 prior to FDA approval to market of the modified device (Special 510(k) K032052, clearance date July 25, 2003) and withdrawn from the field June 25, 2003.

FDAJul 18, 2006CA• Plus Orthopedics USA

Plus Orthopedics USA: UC-PLUS Solution Unicondylar Knee System, Model Numbers:...

There exists the possibility that incomplete bony support or insufficient cementing of the implanted device can result in fatigue fracture of the UC-PLUS Solution Femoral Component.

FDAJul 18, 2006CA• Plus Orthopedics USA

Enpath Medical, Inc: Enpath Lead Adapters, pacemaker lead adapter. Affects: 5...

Enpath Lead Adapters: The internal component (Connector Block) of the Lead Adapter used to secure a lead to the adapter has exhibited varying degress of radial cracks that could cause a temporary intermittent electrical signal disruption if lateral tension is applied to device.

FDAJul 18, 2006CA, MN, NJ• Enpath Medical, Inc

Radiometer America Inc: SafePICO Samplers, self-filling arterial blood samplers. ...

Leaking Tip Caps-Tip caps may leak; after air has been expelled from the syringe through the vented safe tip caps.

FDAJul 18, 2006Nationwide• Radiometer America Inc

CareFree Warm Mist Humidifier (Hunter) – Fire Hazard (2006)

Fire/Burn Risk

The recalled humidifiers are white or black plastic with blue or green tinted water tanks. "Hunter" and "NiteGlo" are printed on the humidifier. The model numbers and tank size included in this recall are listed below. The model number is located on a white label on the bottom of the humidifier. Model Size Description 35201 CareFree® Humidifier Warm Mist 2.0 Gallon White plastic with a blue tinted water tank 35202 CareFree® Humidifier Warm Mist 2.0 Gallon White plastic with a blue tinted water tank 35203 CareFree® Humidifier Warm Mist 2.0 Gallon White plastic with a green tinted water tank 35207 CareFree® Humidifier Warm Mist 2.0 Gallon White plastic with a blue tinted water tank 35253 CareFree® Humidifier Warm Mist 2.0 Gallon Black plastic with a blue tinted water tank

CPSCJul 18, 2006Nationwide• Hunter Fan Co., of Memphis, Tenn.

Enpath Medical, Inc: Angel Medical Systems Lead Adaptor system adapts a St. Ju...

The internal component (Connector Block) of the Lead Adapter used to secure a lead to the adapter has exhibited varying degress of radial cracks that could cause a temporary intermittent electrical signal disruption if lateral tension is applied to device.

FDAJul 18, 2006CA, MN, NJ• Enpath Medical, Inc

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.

ConvaTec: Active Life Non-Convex Drainable Stomahesive pouch-1 1/4...

Cartons labeled 1-1/4 inch size may contain units that are 1-1/2 inch size.

FDAJul 13, 2006Nationwide• ConvaTec

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")

Xoran Technologies, Inc.: Xoran MiniCAT for ENT, Xoran Technologies, Incorporated, ...

The hard drive may crash, resulting in loss of data from patient CT scans.

FDAJul 13, 2006Nationwide• Xoran Technologies, Inc.