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Polaris Industries Inc., of Medina, Minn.

Polaris Industries Inc., of Medina, Minn. Recalls

All product recalls associated with Polaris Industries Inc., of Medina, Minn..

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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 10641–10660 of 10937 recalls

Snowmobile Skis (Polaris) – Accessory Defect (2004)

The recalled skis are the red composite (nonmetallic) skis and were sold as an accessory item for use on Polaris snowmobiles. The part number is inscribed on the tail of the snowmobile ski. The part numbers of the skis are: Part Number Affected Part Number Stamped on Ski Replacement Black Ski (sold individually) 2872291-293 2872291-243 2872291-239 2872291-256 2872492-293 (RMK LH) 2872491-293 (RMK-RH) 1820610-243 1820610-293 5433175 5433175 5433175 5433175 5433260 5433273 5433175 5433175 2872291-070 2872291-070 2872291-070 2872291-070 2872492-070 2872491-070 2872291-070 2872291-070

CPSCFeb 12, 2004Nationwide• Polaris Industries Inc., of Medina, Minn.

General Electric Med Systems: Seneographe 500 Mammography X-Ray Systems (all versions)

The mammography system's information for users lacked the technical specification for the minimum filtration permanently installed in the useful beam and the technical specification for the maximum line current.

FDAFeb 6, 2004Nationwide• General Electric Med Systems

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General Electric Med Systems: Seneographe DMR Mammography X-Ray System (all versions)

FDAFeb 6, 2004Nationwide• General Electric Med Systems

General Electric Med Systems: Seneographe 2000D Digital Mammography X-Ray System

FDAFeb 6, 2004Nationwide• General Electric Med Systems

General Electric Med Systems: Seneographe 800T Mammography X-Ray Systems

FDAFeb 6, 2004Nationwide• General Electric Med Systems

General Electric Med Systems: Seneographe 600 Mammography X-Ray Systems (all versions)

FDAFeb 6, 2004Nationwide• General Electric Med Systems

Varian Medical Systems: EPROM and Control Software (embedded), version 5.08, for ...

Radiation treatment software could potentially cause a healthcare practitioner to apply incorrect treatment regimen to patients undergoing brachytherapy.

FDAFeb 6, 2004Nationwide• Varian Medical Systems

General Electric Med Systems: Seneographe 700T Mammography X-Ray Systems

FDAFeb 6, 2004Nationwide• General Electric Med Systems

Children's Sweatshirts (Meijer) – Drawstring Danger (2004)

The fleece sweatshirts were sold in children's sizes 4-18 under the brand name, "Emergency Exit." The sweatshirts were manufactured in a variety of colors, including red, blue, grey and black. Each sweatshirt has an image on the chest of either a tribal design, dragon, motocross or skateboarding pattern.

CPSCFeb 5, 2004Nationwide• Meijer Distribution Inc., of Grand Rapids, Mich.

Falls Creek Kids Jackets (Meijer) – Size Hazard (2004)

Choking Hazard

The recalled jackets were sold in various colors for boys and girls. Girls' sizes include 2T through 5T, 4 through 7 and 8 through 19. Boys' sizes include 2T through 5T, 4 through 6X and 7/8 through 16. A label inside the jacket reads, "Authentic Falls Creek."

CPSCFeb 5, 2004Nationwide• Meijer Distribution Inc., of Grand Rapids, Mich.

Datex-Ohmeda Inc One Ohmeda: Datex-Ohmeda S/5 and AS/3 Anesthesia Delivery Units (...

Anesthetic agents could be delivered at concentrations above the concentration set on the S/5 and AS/3 Anesthesia Delivery Units (ADU) having serial numbers within a specified range.

FDAFeb 3, 2004Nationwide• Datex-Ohmeda Inc One Ohmeda

Fuji Power Batteries (Dorcy) – Battery Defect (2004)

Fire/Burn Risk

Each of the 3-volt lithium batteries has a white label with the words "Fuji Power" or "A&T Fuji Power CR123A." The batteries were provided separately in pairs in packaging with the flashlights.

CPSCFeb 3, 2004Nationwide• Dorcy International Inc. of Columbus, Ohio

Richard Wolf Medical Instruments Corp.: Pump Tube, REF 8170,121; Suction Pump Drain Tube; An acce...

If the drain tube is assembled incorrectly, the suction pump will not operate as intended.

FDAFeb 2, 2004NE, TX• Richard Wolf Medical Instruments Corp.

Becton Dickinson & Company: BD Test Strips. The US market BD Test Strips are ide...

39 lots of BD Test strip may produce an increased frequency of E-3 messages when used during blood glucose testing.

FDAJan 29, 2004Nationwide• Becton Dickinson & Company

Medtronic Xomed, Inc.: The product is a sheath meant to fit over a Nasopharyngos...

The sheaths in question have shafts that are one inch longer than required for the endoscope specified on the label.

FDAJan 29, 2004FL, ID, IN +12 more• Medtronic Xomed, Inc.

Becton Dickinson & Company: The BD Blood Glucose Monitoring Systems identified as the...

39 lots of BD Test strip may produce an increased frequency of E-3 messages when used during blood glucose testing.

FDAJan 29, 2004Nationwide• Becton Dickinson & Company

Medtronic Xomed, Inc.: Product is a surgical nasal/sinus surgical device labeled...

The curve in the shaft of the bur was only 15 degrees not the labeled 40 degrees.

FDAJan 29, 2004FL, ID, IN +12 more• Medtronic Xomed, Inc.

Medtronic Xomed, Inc.: Product is a device used in adenoid surgery and is labele...

The box label indicates that the product is a size 2 whereas a size 4 was packed inside.

FDAJan 29, 2004FL, ID, IN +12 more• Medtronic Xomed, Inc.

Medtronic MiniMed: Medtronic MiniMed Model 7311 Version 5.0B Solutions Pumps...

A minor software anomaly results in an error in the calculation of the average glucose range that appears on one of the reports available in the model 7311 software.

FDAJan 28, 2004Nationwide• Medtronic MiniMed

Toshiba American Med Sys Inc: Magnetic Resonance Imaging, System: Flexart, Visart and E...

Software anomally causes image slices to be in incorrect order.

FDAJan 27, 2004CA, CO, FL +10 more• Toshiba American Med Sys Inc