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The Valvoline Company, a Division of Ashland Inc., of Lexington, Ky.

The Valvoline Company, a Division of Ashland Inc., of Lexington, Ky. Recalls

All product recalls associated with The Valvoline Company, a Division of Ashland Inc., of Lexington, Ky..

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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 10441–10460 of 10937 recalls

Brake Parts Cleaner (Valvoline) – Chemical Risk (2004)

The recall involves 13-ounce cans of Pyroil® Non-Chlorinated Brake Parts Cleaner and NAPA® Non-Chlorinated Brake Cleaner. This product is used by professional mechanics as well as "do-it-yourself" consumers who perform brake repairs on their own vehicles. The recalled cans contain one of the following four digits in their date codes, which are found on the bottom of the cans: Pyroil (Part No. 4003) C014 C024 C184 C194 C304 D024 D034 D214 D224 D264 E104 F074 F084 F094 F104 F234 F244 F284 G134 G144 G194 G294 H034 H194 NAPA (Part No. 4800) C024 C094 C184 C194 C224 C234 C304 C314 D014 D034 D054 E054 E064 E144 E244 E254 F174 F184 G284 H124 H304 H314 I074 I084

CPSCNov 4, 2004Nationwide• The Valvoline Company, a Division of Ashland Inc., of Lexington, Ky.

Hampton Bay Halogen Light Fixture – Safety Issue (2004)

Fire/Burn Risk

The recall involves the Hampton Bay® three-head, flush-mount, halogen light fixture with silver metal rings on the lamp fixtures. It is 15.75 inches wide by 6 inches high. The lights have frosted glass shades. The position of the three lamps on the fixture can be adjusted by turning and bending the lamp heads. A clear label on the fixture reads "MADE IN CHINA," and "E91785."

CPSCNov 4, 2004Nationwide• Cordelia Lighting, of Rancho Dominguez, Calif.

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Arc Fault Circuit Interrupters (Schneider) – Electrical Defect (2004)

Fire/Burn Risk

The recalled Square D QO® and Homeline® Arc Fault Interrupter circuit breakers are used with 15- and 20-amp branch circuits. They are required to be installed in bedroom circuits in accordance with the 2002 National Electrical Code. The recalled units were manufactured after March 1, 2004, and have a blue test button. The AFCI circuit breakers have one of the following date codes - CN, DN, EN, FN, GN, HN, or JN - stamped in red on the breaker label located just above the wiring terminal. The recalled units also have one of the following catalog numbers printed on a label on the front of the breaker: QO115AFI, QO115AFIC, QO120AFI, QO120AFIC, QOB115AFI, QOB120AFI, HOM115AFI, HOM115AFIC, HOM120AFI, HOM120AFIC, QO115VHAFI, QO120VHAFI, QOB115VHAFI, or QOB120VHAFI.

CPSCNov 3, 2004Nationwide• Schneider Electric North American Division, of Palatine, Ill.

Salsa Campeon Bicycle Forks (Quality Bicycle Products) – Carbon Fiber Defect (2004)

The recall involves carbon fiber/aluminum forks included with the Salsa model F-01 Campeon frame set in either White/Black or Red/Black color combinations. Units included in this recall have a code of CK, DA, or DB and a serial number from 03400 to 04600. The model number, date code and serial number are located on a label at the base of the steerer tube near the crown of the fork.

CPSCNov 2, 2004Nationwide• Quality Bicycle Products, Inc., of Bloomington, Minn.

Boston Scientific Scimed: RunWay 6F Cardiovascular Guide Catheter.

The Runway guide catheter do not meet internal product specifications. Specifically, the affected catheters have exposed or protruding braid wires in the inner lumen of the catheter tip. This condition could have the potential to damage a POBA or Stent Delivery System balloon

FDAOct 29, 2004Nationwide• Boston Scientific Scimed

Medtronic Xomed, Inc.: Brand name: NIM EMG Endotracheal Tube ...

The firm received six reports of tubes with wires 'out of channel' two of which involved injuried patients. In one case in Germany it was reported that the patient had soreness of the throat and was discharged after four days. In the next case the patient had a tracheal wound. It was not clear what caused the wound.

FDAOct 29, 2004Nationwide• Medtronic Xomed, Inc.

Becton Dickinson & Company: ReliOn Insulin Syringe 0.5cc 30 Gauge 5/16 inch (8mm) Nee...

Syringes labeled as 5/16 inch product (30 ga) actually contained the 1/2 inch product (28 ga).

FDAOct 22, 2004AR, TX• Becton Dickinson & Company

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

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