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Yamaha Motor Corporation U.S.A., of Cypress, Calif.

Yamaha Motor Corporation U.S.A., of Cypress, Calif. Recalls

All product recalls associated with Yamaha Motor Corporation U.S.A., of Cypress, Calif..

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

127

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 23781–23800 of 25000 recalls

Yamaha ATVs – mechanical defect (2005)

Laceration Risk

Yamaha has announced a voluntary recall of certain 2005 and 2006 Yamaha Bruin 250, Bruin 350 4WD and 2WD, Big Bear 400, Kodiak 400, and Kodiak 450 ATVs, and certain 2006 Wolverine 450 ATVs. Below is a list of make, model and vehicle identification numbers (VIN) involved in the recall. Make/Model Vehicle Identification Number ("VIN") 2005 Bruin 250 2WD 2006 Bruin 250 2WD 2005 Bruin 350 Auto 2WD 2006 Bruin 350 Auto 2WD 2005 Bruin 350 Auto 4WD 2006 Bruin 350 Auto 4WD 2005 Bruin 350 Auto 4WD Hunter 2006 Bruin 350 Auto 4WD Hunter 2005 Big Bear 400 4WD 2006 Big Bear 400 4WD 2005 Kodiak 400 4WD 2006 Kodiak 400 4WD 2005 Kodiak 400 4WD/Hunter 2006 Kodiak 400 4WD/Hunter 2005 Kodiak 450 4WD 2005 Kodiak 450 4WD 2005 Kodiak 450 4WD/Hunter 2005 Kodiak 450 4WD/Hunter 2005 Kodiak 450 4WD SE 2006 Wolverine 450 4WD YFM250BT YFM250BV YFM350BAT YFM350BAV YFM350FAT YFM350FAV YFM350FAHT YFM350FAHV YFM400FT YFM400FV YFM400FAT YFM400FAV YFM400FAHT YFM400FAHV YFM450FAT YFM450FAV YFM450FAHT YFM450FAHV YFM450FASET YFM450FXV AG01Y-0116001 ~ 0120900 AG01Y-0120901 ~ 0123400 AH10Y-0012901 ~ 0016600 AH10Y-0016601 ~ 0020100 AH09Y-0019301 ~ 0023500 AH09Y-0023501 ~ 0029400 AH13Y-0002601 ~ 0003600 AH13Y-0003601 ~ 0006100 AH06Y-0055101 ~ 0057600 AH06Y-0057601 ~ 0059281 AJ15Y-0000101 ~ 0009600 AJ15Y-0009601 ~ 0011700 AJ17Y-0000101 ~ 0002100 AJ17Y-0002101 ~ 0003200 AJ14Y-0000101 ~ 0014900 AJ14Y-0014901 ~ 0018800 AJ16Y-0000101 ~ 0005300 AJ16Y-0005301 ~ 0008300 AJ18Y-0000101 ~ 0002700 AJ21Y-0000101 ~ 0001400

CPSCNov 2, 2005Nationwide• Yamaha Motor Corporation U.S.A., of Cypress, Calif.

Radiometer America Inc: D826 Accessory kit for single tcpO2 Electrodes for use wi...

Excessive Drift-the membrane units of the device cause the electrode to exceed performance standards for drift in the first two or more calibrations

1...1188 118911901191 1192...1250

Page 1190 of 1250Next

FDANov 1, 2005AL, AK, AZ +39 more• Radiometer America Inc

Terumo Cardiovascular Systems Corp: Terumo Advanced Perfusion System 1; 100V -120V, 15 A (cir...

The power manager subsystem may not initialize properly during start-up, which will cause the battery status monitoring and battery switching operations to not be fully functional.

FDANov 1, 2005Nationwide• Terumo Cardiovascular Systems Corp

Animas Corporation: Isulin Pump. Model IR1000

Pumps were refurbished more than one time for the same failure mode in violation of the company's procedure.

FDAOct 31, 2005CA, CO, FL +13 more• Animas Corporation

Animas Corporation: Isulin Pump. Model IR1250

Pumps were refurbished more than one time for the same failure mode in violation of the company's procedure.

FDAOct 31, 2005CA, CO, FL +13 more• Animas Corporation

Animas Corporation: Isulin Pump. Models R1000

Pumps were refurbished more than one time for the same failure mode in violation of the company's procedure.

FDAOct 31, 2005CA, CO, FL +13 more• Animas Corporation

Radiometer America Inc: S1730 Calibration Solution 2, 200 mL, packed in single un...

Calibration solution for ABL700 Blood Gas Analyzers is labeled with an incorrect bar code. The bar code identified on the Cal Solution 2 product is actually the bar code for the rinse solution.

FDAOct 31, 2005Nationwide• Radiometer America Inc

Radiometer America Inc: ABL800 Series Blood Gas Analyzer equipped with Software V...

ABL800 Series Blood Gas Analyzer became inoperable when the 'restore default setup' button was touched.

FDAOct 31, 2005Nationwide• Radiometer America Inc

Animas Corporation: Isulin Pump. Model IR1200

Pumps were refurbished more than one time for the same failure mode in violation of the company's procedure.

FDAOct 31, 2005CA, CO, FL +13 more• Animas Corporation

Newport Medical Instruments Inc: Newport HT50 All Purpose Ventilator

Lack of alarm prior to shutdown.

FDAOct 29, 2005Nationwide• Newport Medical Instruments Inc

Abbott Molecular: Vysis LSI p16 (9p21)/CEP 9 (9p11-q11) Dual Color Probe Se...

The DNA-Probe has a target size of ~300 Kb region instead of the labeled ~190 Kb region.

FDAOct 28, 2005Nationwide• Abbott Molecular

Battery Ride-On Vehicles (Dorel) – operational risk (2005)

Fire/Burn Risk

The recalled battery-powered ride-on vehicles include the Pink Corvette®, Torch Red Corvette®, Yellow Race Car Corvette®, Red Electroplate Corvette®, Fire Engine, and Batmobile® with the model numbers listed in the chart below. They were sold under the brands Safety 1st and Kid Trax by Safety 1st. The ride-on vehicles were manufactured between January 2004 and August 2005. The manufacture date is located on the underside of the unit and is molded into the plastic body as shown below. The circle on left displays the month of manufacture, the circle on the right displays the year of manufacture. The model numbers are located on the underside of the vehicles near the date code. Ride-On Vehicle Name Model Safety 1st Pink Corvette® 50503/50503A Safety 1st Torch Red Corvette® 50504/50504A Safety 1st Yellow Race Car Corvette® 50505/50505A Safety 1st Red Electroplate Corvette® 50521/50521A Kid Trax Fire Engine 50506/50506A Safety 1 st Batmobile® 50527

CPSCOct 27, 2005Nationwide• Dorel Juvenile Group USA, of Columbus, Ind.

ela Medical Llc: Symphony DR model 2550 and ELA Rhapsody DR model 2510. A...

Through post-market surveillance, ELA Medical has observed that a no-output condition could occur in a limited number of Symphony or rhapsody pacemakers. The no-output condition could occur due to metal migration caused by a specific manufacturing process.

FDAOct 25, 2005AZ, CA, FL +7 more• ela Medical Llc

ela Medical Llc: ELA Rhapsody SR model 2210. A single chamber rate-respon...

FDAOct 25, 2005AZ, CA, FL +7 more• ela Medical Llc

Gambro Renal Products, Inc.: Gambro Prisma M100 preset, Part No. 8353486.

After dialysis machine is disconnected from the patient, blood leakage may occur while unloading the tubing sets from the machine.

FDAOct 24, 2005Nationwide• Gambro Renal Products, Inc.

Gambro Renal Products, Inc.: Gambro Prisma HF1000 preset, Part No. 8399050.

After dialysis machine is disconnected from the patient, blood leakage may occur while unloading the tubing sets from the machine.

FDAOct 24, 2005Nationwide• Gambro Renal Products, Inc.

Merit Medical Systems, Inc: Viceroy Inflation Syringe, 60mL, Sterile, Rx only.

Inflation device may not hold vacuum during angioplasty procedure.

FDAOct 21, 2005FL, OR, UT• Merit Medical Systems, Inc

Eastman Kodak Co: KODAK DirectView DR 7100 System, Catalog # 133-6049. Thi...

Potential weld defect in the Overhead Tube Support assembly which connects the tube assembly to the telescoping arm. This could cause the tube assembly to fall, injuring anyone near the unit.

FDAOct 20, 2005FL, IN, KY +5 more• Eastman Kodak Co

In-Wall Volume Controls (Dana Innovations) – installation risk (2005)

Fire/Burn Risk

Sold under the brand names Architectural Audio and HomeTech, these in-wall volume controls were professionally installed as part of whole house audio systems. The switch plate covers for the recalled systems are white or almond, and "aVc" (amplified volume control) is imprinted above the volume control. They have the following model numbers: Brand Model Numbers Architectural Audio 20127 20128 HomeTech 10114 10115 The model number is not visible to the consumer, and consumers are instructed not to remove the keypads from the wall to look for a model number. All serial numbers are included in the recall.

CPSCOct 20, 2005Nationwide• Dana Innovations, of San Clemente, Calif.

Gas-Packs (International Comfort) – heating malfunction (2005)

The recall involves certain limited "Gas-Packs" sold under the brand names Airquest, Arcoaire, Comfortmaker, Heil, Keeprite, Kenmore, ICP Commercial, and Tempstar. The affected units were manufactured between the 41st week of 2000 and the 26th week of 2003, and are installed outside the home. The model and serial numbers of affected units are printed on the unit's rating plate, as shown in the photo. Model numbers appear in the following typical format: PGC036K060A; serial numbers appear in the following typical format: L004112345. Affected models begin with PGC, PGF, PGS, GPFM, GPSM, or GPCM. Please contact the ICP phone number with the complete model and serial number from your unit, or visit www.icpusa.com, for assistance in determining whether your unit is covered.

CPSCOct 19, 2005Nationwide• International Comfort Products LLC, of Lewisburg, Tenn.