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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

899

Class I (Serious)

125

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 16861–16880 of 17592 recalls

Polaris RANGER 4x4 Utility Vehicle (Polaris) – Vehicle Safety Concern (2004)

All model year 2005 "RANGER 4x4" Utility Vehicles with model number R05RD50AA are part of this recall. The model number is located on the upper right frame tube directly under the right side of the seat. The RANGER 4x4 Utility Vehicles have black seats with a green chassis. "RANGER 4x4" is prominently displayed on the right and left side of the rear cargo box.

CPSCOct 21, 2004Nationwide• Polaris Industries, Inc., of Medina, Minn.

General Electric Med Systems LLC: Patient tables of CT systems with brand name: CT/e; CT/e ...

The patient tables of the affected CT systems are supported by a hydraulic cylinder and a cylinder shaft (i.e. the upper shaft) which connects the tabletop to the table frame. GE received a report of a HiSpeed LX/I system table falling abruptly due to the filure of the upper shaft. No injuries were reported.

FDAOct 21, 2004Nationwide• General Electric Med Systems LLC

BD Diagnostic Systems: BD, Brucella melitensis Antigen

1...842 843844845 846...880

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Febrile Antigens and Control Antisera that were released prior to August 2003 contained the 12/2000 revised insert that had incorrect testing instructions.

FDAOct 20, 2004Nationwide• BD Diagnostic Systems

BD Diagnostic Systems: BD, Salmonella O Group B Antigen (1-4-5-12)

Febrile Antigens and Control Antisera that were released prior to August 2003 contained the 12/2000 revised insert that had incorrect testing instructions.

FDAOct 20, 2004Nationwide• BD Diagnostic Systems

BD Diagnostic Systems: BD, Salmonella O Group A Antigen (1-2-12)

Febrile Antigens and Control Antisera that were released prior to August 2003 contained the 12/2000 revised insert that had incorrect testing instructions.

FDAOct 20, 2004Nationwide• BD Diagnostic Systems

BD Diagnostic Systems: BD, Proteus OX19 Antigen

Febrile Antigens and Control Antisera that were released prior to August 2003 contained the 12/2000 revised insert that had incorrect testing instructions.

FDAOct 20, 2004Nationwide• BD Diagnostic Systems

BD Diagnostic Systems: BD, Salmonella O Group D Antigen (9-12) (Typhoid O)

Febrile Antigens and Control Antisera that were released prior to August 2003 contained the 12/2000 revised insert that had incorrect testing instructions.

FDAOct 20, 2004Nationwide• BD Diagnostic Systems

BD Diagnostic Systems: BD, Salmonella Flagellar Polyvalent Antiserum (a,b,d)

Febrile Antigens and Control Antisera that were released prior to August 2003 contained the 12/2000 revised insert that had incorrect testing instructions.

FDAOct 20, 2004Nationwide• BD Diagnostic Systems

BD Diagnostic Systems: BD, Brucella abortus Antigen

Febrile Antigens and Control Antisera that were released prior to August 2003 contained the 12/2000 revised insert that had incorrect testing instructions.

FDAOct 20, 2004Nationwide• BD Diagnostic Systems

BD Diagnostic Systems: BD, Proteus Polyvalent Antiserum (OXK, OX2, OX19)

Febrile Antigens and Control Antisera that were released prior to August 2003 contained the 12/2000 revised insert that had incorrect testing instructions.

FDAOct 20, 2004Nationwide• BD Diagnostic Systems

BD Diagnostic Systems: BD, Brucella Postive Control Antiserum (AMS)

Febrile Antigens and Control Antisera that were released prior to August 2003 contained the 12/2000 revised insert that had incorrect testing instructions.

FDAOct 20, 2004Nationwide• BD Diagnostic Systems

Zippo MPL Multi-Purpose Lighter (Zippo) – Fuel Safety Concern (2004)

Fire/Burn Risk

The Zippo MPL (Multi-Purpose Lighter) uses refillable butane fuel, is child resistant, and measures 8 inches long and 1 inch wide. The utility lighter is finished in black metal or silver metal with a chrome nozzle. The black unit is packaged in a blister pack with black and red graphics and the silver unit is in a silver gift box. Only utility lighters with these date codes are recalled: G03, H03, I03, ZH03. The date code is on the black adjuster knob on the bottom of the lighter.

CPSCOct 20, 2004Nationwide• Zippo Manufacturing Company, of Bradford, Pa.

BD Diagnostic Systems: BD, Salmonella Flagellar d Antigen (Typhoid H)

Febrile Antigens and Control Antisera that were released prior to August 2003 contained the 12/2000 revised insert that had incorrect testing instructions.

FDAOct 20, 2004Nationwide• BD Diagnostic Systems

BD Diagnostic Systems: BD, Francisella tularensis Antigen

Febrile Antigens and Control Antisera that were released prior to August 2003 contained the 12/2000 revised insert that had incorrect testing instructions.

FDAOct 20, 2004Nationwide• BD Diagnostic Systems

Medtronic Inc. Cardiac Rhythm Managment: Medtronic CapSureFix Novus Lead Model 5076.

A specific lot of leads are labeled incorrectly. The leads are 45 cm in length and labeled as 52 cm lead length.

FDAOct 20, 2004Nationwide• Medtronic Inc. Cardiac Rhythm Managment

BD Diagnostic Systems: BD, Febrile Antigen Negative Control

Febrile Antigens and Control Antisera that were released prior to August 2003 contained the 12/2000 revised insert that had incorrect testing instructions.

FDAOct 20, 2004Nationwide• BD Diagnostic Systems

BD Diagnostic Systems: BD, Salmonella Somatic Polyvalent Antiserum (A,B,D)

Febrile Antigens and Control Antisera that were released prior to August 2003 contained the 12/2000 revised insert that had incorrect testing instructions.

FDAOct 20, 2004Nationwide• BD Diagnostic Systems

Avanti Water Dispenser (Avanti) – Hot Water Faucet Risk (2004)

Fire/Burn Risk

There are six models of water dispensers with hot water faucets included in the recall. The water dispensers have "Avanti" written on the front of the base. They have model number WD32, WD 50, WD 50.1, WDT51, WDR 52 or WHC 59. The model number is written on a silver sticker on the back of the unit. Model number WDR 52 is a combination refrigerator and water dispenser. All six models have removable drip trays and can hold either 3- or 5-gallon bottles of water.

CPSCOct 19, 2004Nationwide• Avanti Products Inc., of Miami, Fla.

Merit Medical Systems, Inc: Custom Convenience Kit

Merit Custom Convenience Kits contain Monoject Magellan safety needles which have been recalled by Tyco Healthcare.These needles may detach from their hub during use.

FDAOct 15, 2004Nationwide• Merit Medical Systems, Inc

Merit Medical Systems, Inc: Safety Paracentesis Procedure Tray

Merit Safety Paracentesis Procedure Trays contain Monoject Magellan safety needles which have been recalled by Tyco Healthcare.These needles may detach from their hub during use.

FDAOct 15, 2004Nationwide• Merit Medical Systems, Inc