Stay Informed

Get email alerts when new recalls match your interests.

Recall data is updated hourly from official government sources. Very recent recalls may not yet appear. About our data sources

About

We make U.S. recall data searchable and accessible for consumers and businesses.

Site

FAQ
Browse by State
Statistics
Recall Classifications
About
Enterprise API

Legal

Privacy Policy
Terms of Service
Report Incorrect Info

Official Sources

FDA Recalls ↗
USDA FSIS ↗
CPSC Recalls ↗
NHTSA Recalls ↗

RSS Feed

Home
/
Brands
/
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..

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

620

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 10061–10080 of 10937 recalls

Snowmobiles (Arctic Cat) – Fire and Burn Risk (2006)

Fire/Burn Risk

The recalled fuel tanks were installed on all 2004, 2005 and 2006 Firecat and Sabercat models. The recall also includes all 2003 Firecat carbureted models. The affected models were manufactured in a variety of colors and engine sizes. However, all are included in this recall.

CPSCApr 25, 2006Nationwide• Arctic Cat Inc., of Thief River Falls, Minn.

J. Jamner Surgical Instruments, Inc.: Ruggles Leyla Ball Joint Clamp, MODEL/CATALOG #: R2383 ...

The Ruggles Leyla Ball Joint Clamp may not properly tighten onto the Rigid Holding Rod. Although this condition can be observed during assembly, if the device were to be used during surgery, any attachments to the Rigid Holding Rod could move.

FDAApr 24, 2006IL, IN, MS +2 more• J. Jamner Surgical Instruments, Inc.

Emergency Smoke Hoods (EVAC) – Carbon Monoxide Risk (2006)

Fire/Burn Risk

1...502 503504505 506...547

Page 504 of 547Next

These smoke hoods are one-time use respiratory devices that assist users with breathing, while escaping a fire. They include a transparent plastic hood that covers the user's head, and a canister that filters out toxic gases. "EVAC+™" or "EVAC-U8™" is printed on the canister.

CPSCApr 20, 2006Nationwide• Brookdale International Systems Inc., of Vancouver, British Columbia, Canada

Edwards Lifesciences Research Medical, Inc.: Duraflo Treated Aortic Perfusion Cannula with plastic tip...

Due to potential embrittlement of the plastic tip which may crack or separate during use.

FDAApr 18, 2006CA, CT, FL +7 more• Edwards Lifesciences Research Medical, Inc.

Camming Anchor (CCH) – Fall Hazard (2006)

These camming anchors or "Alien Cams" are devices used as both a precautionary measure to stop a climber in the event of falls, or it is used to actually support the climber. Climbers insert the device into cracks or crevasses in rock and it grips the sides of the crack. The recalled units are marked with a small center punch dimple at the base of the round ball where the axle goes through the cable eye. They have production dates, from November 2004 (written as 1104) through December 2005 (written as 1205), which can be found on the bottom of the handle puller.

CPSCApr 18, 2006Nationwide• Colorado Custom Hardware (CCH) Inc., of Laramie, Wyo.

Edwards Lifesciences Research Medical, Inc.: Aortic Perfusion Cannula with Metal Tip, 22 Fr. x 23 cm. ...

Due to potential embrittlement of the overmolded plastic portion of the metal tip which may crack or separate during use.

FDAApr 18, 2006CA, CT, FL +7 more• Edwards Lifesciences Research Medical, Inc.

Edwards Lifesciences Research Medical, Inc.: Aortic Perfusion Cannula with plastic tip, 22 Fr. x 28 cm...

Due to potential embrittlement of the plastic tip which may crack or separate during use.

FDAApr 18, 2006CA, CT, FL +7 more• Edwards Lifesciences Research Medical, Inc.

Electric Mobility Corp: Rascal 600F and 600T scooters, unspecified power wheelchair.

The four seat mast mounting screws can loosen, causing seat to wobble. The chair seat actuator and portions of the seat can malfunction and/or break. Firm is aware of problems with the seat and injuries sustained from the powered wheelchair/scooter seat malfunction. Firm has not initiated recall, claims it is a Warranty Advisory.

FDAApr 17, 2006Nationwide• Electric Mobility Corp

Toe-Kick Saws (Crain) – Broken Handles (2006)

Laceration Risk

The saws are used for the removal of floors or cutting flooring in the toe kick area under cabinets. Only Model 795, which has a blue handle and motor housing, is included in this recall. "Model 795" and "Crain Toe-Kick Saw" are printed on a label on the blue motor housing.

CPSCApr 13, 2006Nationwide• Crain Cutter Co. Inc., of Milpitas, Calif.

Kamiya Biomedical Company: K-ASSAY CRP(2) Reagent. Kit is labeled K-ASSAY CRP (2) L...

Kits may contain 2 vials of the same reagent instead of 1 vial of buffer reagent and 1 vial of antibody reagent

FDAApr 11, 2006Nationwide• Kamiya Biomedical Company

Snowmobiles (Polaris) – Steering Hazard (2006)

The recall includes Polaris Model Year 2006 700IQ Classic, 700 IQ Touring, Select Model Year 2005 900 Fusion, 900 RMK, 900 Switchback, Select Model Year 2006 700 IQ Fusion, RMK, and Select Model Year 2006 900 Fusion, RMK Switchback Snowmobiles with Accessory Electric Start Kits. The model and serial number (VIN) identification decal is located on the right-side of the tunnel underneath the seat. The model and serial number (VIN) identification decal is located on the right-side of the tunnel underneath the seat. The table below lists all models possibly affected by the recall. Model(s) Affected Model Numbers 2005 900 Fusion (With Accessory Electric Start Kit) S05MP8DS (A)(B)(C) 2005 900 Switchback (With Accessory Electric Start Kit) S05PS8DS 2005 900 RMK (With Accessory Electric Start Kit) S05PL8DS (A)(B)(C)(D) S05PL8DEB S05PM8DS (A)(B) S05PN8DS S05PN8DE 2006 700 Classic (Electric Start Standard) S06PD7HS 2006 700 Touring (Electric Start Standard) S06PT7HS S06PT7HE 2006 700 Fusion (With Snow Check Select Option or Accessory Electric Start Kit) S06MP7HS (A)(B) S06ME7HS 2006 700 RMK (With Snow Check Select Option or Accessory Electric Start Kit) S06PK7HS (A)(B) S06PL7HS (A)(B) S06PM7HS (A) 2006 900 Fusion (With Snow Check Select Option or Accessory Electric Start Kit) S06MP8DS (A)(B) S06ME8DS 2006 900 Switchback (With Snow Check Select Option or Accessory Electric Start Kit) S06PS8DS (A) 2006 900 RMK (With Snow Check Select Option or Accessory Electric Start Kit) S06PL8DS (A)(B) S06PM8DS (A) S06PN8DS (A) S06PR8DS Note: Not all Model Year 2005 and 2006 snowmobiles are affected.

CPSCApr 11, 2006Nationwide• Polaris Industries Inc., of Medina, Minn.

Northwest Medical Physics Equipment Inc: ISOLOC 6.5 Software Part Number NT-NW-425-520. Software ...

This correction was for several software bugs which caused image format problems; incorrect ruler display; software crashes; failure to update pixel spacing; display of unattainable treatment table positions; failure to update gantry angles; wrong shifts for two of three axes of treatment table movement.

FDAApr 7, 2006IN• Northwest Medical Physics Equipment Inc

InMotion Trampolines – Injury Risk (2006)

The round, black mini-trampoline measures 36 inches across and has six 7½-inch long metal legs. The mini-trampoline is used for in-place jogging and other cardiovascular exercises. Most mini-trampolines that have model numbers containing 35-1625 are included in the recall. Model 35-1625C and 35-1625CW units are not included in the recall. The model number, along with the customer service and serial numbers, are stamped on a black and white label on one of the legs, containing the name "Stamina."

CPSCApr 6, 2006Nationwide• Stamina Products Inc., of Springfield, Mo.

Philips Medical Systems North America Co. Phillips: MD3 X-ray system

Potential for unexpected table movement.

FDAApr 6, 2006Nationwide• Philips Medical Systems North America Co. Phillips

Philips Medical Systems North America Co. Phillips: MD4 X-ray system

Potential for unexpected table movement.

FDAApr 6, 2006Nationwide• Philips Medical Systems North America Co. Phillips

LandRoller Terra 9 Roller Skates (LandRoller) – Balance Design (2006)

LandRoller skates have two oversized wheels on each skate that are angled inward, which is designed to help the user keep balanced on cracked pavement and uneven surfaces. The recalled LandRoller brand skates are the "Terra 9" model manufactured between July 2005 and December 2005. The date of manufacture can be determined from the serial number, which is written on a white sticker attached to the upper inside of the right boot's plastic ankle cuff. Serial numbers beginning with "L050" are included in the recall. The brand name is on the skate's tongue and model is on the skate's rear heel area. Women's skates are purple and gray and sold in sizes 6 through 11. Men's skates are blue and black and sold in sizes 5 through 12.

CPSCApr 5, 2006Nationwide• LandRoller Inc., of Hermosa Beach, Calif.

Massaging Bed Rest (Brookstone) – Burn Hazard (2006)

Fire/Burn Risk

The recalled bed rest is designed to support a person sitting in bed. It is beige and consists of a back, two foldable armrests with a cup holder and massage controls, and a headrest with a reading light attached. "Imported by Brookstone Company" is printed on a tag attached to the bed rest. The massaging bed rest also provides heat at a single setting. A curly beige cord is attached to the back lower left corner of the bed rest. On some of the bed rests, "SKU NO: 431254" is printed on a round metal plate where the curly beige cord plugs into the bed rest. "Brookstone" is printed on the beige plug-in transformer that attaches to the beige cord.

CPSCApr 4, 2006Nationwide• Brookstone Company Inc., of Merrimack, N.H.

Disetronic Medical Systems, Inc.: Disetronic Ultraflex 8/80 infusion set; Catalog number 44...

The luer tube may break at the lock-tubing connection to the pump, causing an interruption of insulin delivery, which can and has contributed to hyperglycemia

FDAMar 31, 2006Nationwide• Disetronic Medical Systems, Inc.

Disetronic Medical Systems, Inc.: Accu-Chek Ultraflex-2 infusion set; 8 mm 24'' (60 cm); Ca...

The luer tube may break at the lock-tubing connection to the pump, causing an interruption of insulin delivery, which can and has contributed to hyperglycemia

FDAMar 31, 2006Nationwide• Disetronic Medical Systems, Inc.

Disetronic Medical Systems, Inc.: Accu-Chek Ultraflex-8 infusion set; Catalog number 454477...

The luer tube may break at the lock-tubing connection to the pump, causing an interruption of insulin delivery, which can and has contributed to hyperglycemia

FDAMar 31, 2006Nationwide• Disetronic Medical Systems, Inc.