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Arctic Cat Inc., of Thief River Falls, Minn.

Arctic Cat Inc., of Thief River Falls, Minn. Recalls

All product recalls associated with Arctic Cat Inc., of Thief River Falls, Minn..

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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 34361–34380 of 37665 recalls

Arctic Cat Snowmobile – Steering Failure (2006)

Fire/Burn Risk

The recalled steering shafts were installed on the following models: All 2002 440 Sno Pro Models All 2003 Firecat 500/600/700, Firecat 700 Sno Pro, and 440 Sno Pro Models All 2004 Firecat 500/600/700 (STD and Sno Pro), and Sabercat 500/600/700 Models All 2005 Firecat 500/600/700 (STD and Sno Pro), M5,M6,M7, and Sabercat 500/600/700 Models All 2006 Crossfire 600/700, Firecat 500/600/700, Firecat 700 Sno Pro, Sabercat 500/600/700, and all M-Series

CPSCSep 19, 2006Nationwide• Arctic Cat Inc., of Thief River Falls, Minn.

Abbott Laboratories: Abbott brand CELL-DYN 22 Calibrator, a whole blood calibr...

Potential for on-market instability in the whole blood calibrator which could lead to inaccurate platelet (PLT) test results.

FDASep 18, 2006PR• Abbott Laboratories

Datex Ohmeda, Inc: Datex-Ohmeda Tec 6 Plus Desflurane Vaporizer. It is an e...

There is a possibility of a vaporizer power failure, with audible and visual alarms, when using the Tec 6 Plus Desflurane Vaporizer.

1...1717 171817191720 1721...1884

Page 1719 of 1884Next

FDASep 15, 2006Nationwide• Datex Ohmeda, Inc

Whiteside Biomechanics: Posterior Acetabular Retractor-Left with Light Cord Brack...

The soft tissue pin in the retractor can break off and become embedded in the tissue.

FDASep 15, 2006IN, MD, MO• Whiteside Biomechanics

GE OEC Medical Systems, Inc: InstaTrak with Multiple Dataset Navigation, 892.2050 Syst...

Please be aware that this is not a new recall. The firm has taken action; but, due to administrative issues this recall is now being classified by the Agency. On October 11, 2006, GE Healthcare recalled GE OEC InstaTrak 3500 Plus System with Software version 5.2, the surgical Navigation and Visualization Application due to software related issues.

Class IHigh

FDASep 15, 2006Nationwide• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: InstaTrak with Multiple Dataset Navigation, 892.2050 Syst...

FDASep 15, 2006Nationwide• GE OEC Medical Systems, Inc

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

Failure to initiate compressions when turned on.

FDASep 14, 2006Nationwide• Michigan Instruments, Inc.

Terumo Cardiovascular Systems Corp: Terumo Perfusion System 9000, 100v, with color screen; Mo...

The hand crank handle may separate and detach from the unit during use.

FDASep 14, 2006Nationwide• Terumo Cardiovascular Systems Corp

Terumo Cardiovascular Systems Corp: Terumo Perfusion System 8000 Base, 4 pump, 115v; Model 80...

The hand crank handle may separate and detach from the unit during use.

FDASep 14, 2006Nationwide• Terumo Cardiovascular Systems Corp

Terumo Cardiovascular Systems Corp: Manual Drive Unit for Sarns (Terumo) Centrifugal Perfusio...

The hand crank handle may separate and detach from the unit during use.

FDASep 14, 2006Nationwide• Terumo Cardiovascular Systems Corp

Terumo Cardiovascular Systems Corp: Terumo Perfusion System 9000, 220/240v, with color screen...

The hand crank handle may separate and detach from the unit during use.

FDASep 14, 2006Nationwide• Terumo Cardiovascular Systems Corp

True Religion Hoodie – Strangulation Risk (2006)

The recalled hoodies have a drawstring through the hood. The products are black, pink, or blue and were sold in children's sizes XS, S, M, L, and XL. The True Religion horseshoe design is displayed on the front of the hoodie. The name "True Religion" appears inside the hoodie.

CPSCSep 14, 2006Nationwide• True Religion, of Los Angeles, Calif.

Depuy Orthopaedics, Inc.: Depuy PFC Oval Dome Patella (Part Number 960100)3-Peg, 3...

Mislabeled: units containing a size 32 mm. patella were labeled as a 38 mm patella.

FDASep 14, 2006Nationwide• Depuy Orthopaedics, Inc.

Medtronic Perfusion Systems: Medtronic Intersept Custom Tubing Pack. Do Not Reuse. T...

An out of specification condition exists with the tapered tubing found in some Custom Tubing Packs. The wall thickness is undersized and does not meet specifications.

FDASep 13, 2006CA, FL, IL +3 more• Medtronic Perfusion Systems

John Deere Grill – Fire Risk (2006)

Fire/Burn Risk

These are John Deere Gas Barbecue Grills with model numbers HR-BG6203 and HR-BG5202. The model number is on the CSA approval sticker on the back panel. The recalled grills have a John Deere symbol on the center of the hood and a John Deere decal plate below the control panel. These are 52,000 BTU grills with 460 sq. in. cooking surface. The Model HR-BG6203 includes stainless steel doors, stainless steel side shelves and a side burner rated at 10,000 BTU. The Model HR-BG5202 has stainless steel doors with black plastic side shelves.

CPSCSep 13, 2006Nationwide• Onward Manufacturing, of Waterloo, Ontario, Canada

GE OEC Medical Systems, Inc: GE OEC 9900 Elite Fluoroscopy System with Integrated Navi...

Missing, mixed or lost patient images may result after X-ray procedures. Error in navigation accuracy.

FDASep 13, 2006FL, GA, IL +11 more• GE OEC Medical Systems, Inc

Beckman Coulter Inc: Coulter LH700 Series Hematology Analyzers, Part Number 66...

There is a potential for erroneous yet credible results for Body Fluids on the LH700 series hematology analyzers when a cassette label fails to read and the subsequent sample is cycled in Body Fluid mode.

FDASep 12, 2006Nationwide• Beckman Coulter Inc

Bioplate Inc: Bioplate Resorbable Bone Fixation Tack, Catalog Number: ...

Lack of device sterilization: An internal investigation found products were released for distribution labeled as sterile, but the lot was not sterilized.

FDASep 12, 2006Nationwide• Bioplate Inc

Varian Medical Systems: GammaMed 12it radionuclide applicator system, Varian Medi...

Medical device for patient treatment does not meet electrical safety standards.

FDASep 11, 2006AZ, GA, IL +2 more• Varian Medical Systems

Varian Medical Systems: GammaMed 12i radionuclide applicator systems, distributed...

Medical device for patient treatment does not meet electrical safety standards.

FDASep 11, 2006AZ, GA, IL +2 more• Varian Medical Systems