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Nikon Inc., of Melville, N.Y.

Nikon Inc., of Melville, N.Y. Recalls

All product recalls associated with Nikon Inc., of Melville, N.Y..

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Recall Summary

Total Recalls

1000

Past Year

898

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 16521–16540 of 17592 recalls

Nikon Battery Packs (EN-EL3) – potential failure (2005)

Fire/Burn Risk

The recall involves the Nikon rechargeable lithium-ion battery pack with model number EN-EL3, which is written on the side of the battery. The batteries are rated at 7.4V/1400mAh, which also is written on the battery. The battery is included as a power source for Nikon's digital SLR D100, D70, and D50 model cameras. The battery pack was also sold separately.

CPSCNov 8, 2005Nationwide• Nikon Inc., of Melville, N.Y.

Merit Medical Systems, Inc: IntelliSystem II Thermal Dot Matrix printer 110 V adapter...

Fire/Burn Risk

Dot matrix printer, as a component of a pressure monitoring system, may overheat and pose a fire hazard.

FDANov 7, 2005AL, IN, MD +8 more• Merit Medical Systems, Inc

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

1...825 826827828 829...880

Page 827 of 880Next

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

Wilson-Cook Medical Inc: Fusion OMNI- GT * DOME TIP: ERCP Catheter: 6.0 FR./200 CM...

Misbranded; The catheter size listed on the product label is 6 French, which is inaccurate. The catheter size is more accurately described as 7 French.

FDAOct 31, 2005Nationwide• Wilson-Cook Medical Inc

Newport Medical Instruments Inc: Newport HT50 All Purpose Ventilator

Lack of alarm prior to shutdown.

FDAOct 29, 2005Nationwide• Newport Medical Instruments Inc

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.

Becton Dickinson & Company: BD 1 mL Allergist tray with 26G x 3/8 in. BD Safety Glide.

Safety mechanisms on the syringes are rotating too freely. This can result in the safety mechanism not holding its rotational position and increasing risk of an accidental needle-stick.

FDAOct 25, 2005Nationwide• Becton Dickinson & Company

Becton Dickinson & Company: BD 1 mL Allergist tray with 27 G x 1/2 in. BD Safety Glide.

Safety mechanisms on the syringes are rotating too freely. This can result in the safety mechanism not holding its rotational position and increasing risk of an accidental needle-stick.

FDAOct 25, 2005Nationwide• Becton Dickinson & Company

Becton Dickinson & Company: BD 1 mL BD Safety Glide tuberculin syringe with 27 G x 1/...

Safety mechanisms on the syringes are rotating too freely. This can result in the safety mechanism not holding its rotational position and increasing risk of an accidental needle-stick.

FDAOct 25, 2005Nationwide• Becton Dickinson & Company

Shag Leather Rugs (Hellenic) – quality issue (2005)

Fire/Burn Risk

The recall includes only beige and champagne leather shag rugs with Hellenic's name on the label. Large sizes include 5 feet by 8 feet and 8 feet by 11 feet and small sizes include 3 feet 5 inches by 5 feet 5 inches, 2 feet by 3 feet and 2 feet by 8 feet. A label on the rugs reads, "Hellenic Rug Imports, Inc."

CPSCOct 25, 2005Nationwide• Hellenic Rug Imports Inc., of Brooklyn, N.Y.

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

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.

Terumo Cardiovascular Systems Corp: Terumo Sarns brand Soft-Flow Aortic Cannula with flange, ...

The product is labeled as sterile, but the firm has determined that the suture flange may tear through the front of the package.

FDAOct 19, 2005CA, IN, MO• Terumo Cardiovascular Systems Corp

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

While on battery power, the system may flash a low battery warning even though the battery is adequately charged.

FDAOct 19, 2005Nationwide• Terumo Cardiovascular Systems Corp

Jumbo Pencils with Sharpeners (Target) – Potential Safety Issue (2005)

Laceration Risk

The jumbo pencil has a red eraser on the end and comes with a pencil sharpener. Pencils are either short, 8 ½ inches long and one inch wide, or long, 15 inches long and ½ inch wide. The pencils are blue, red or striped. The sharpeners are pink or blue and come in a clear plastic pouch. Model number 70505 is printed on the pouch.

CPSCOct 18, 2005Nationwide• Target Corp., of Minneapolis, Minn.

Applied Medical Resources Corp 22872 Avenida Empresa # 3 Rancho Santa: The Applied GelPort Hand Access Device consists of a GelS...

The Applied GelPort Laparoscopic Hand Access Device, Model C8004. product is being recalled due to an incorrect component. The incorrect Wound Retractor base was packaged with the kit.

FDAOct 17, 2005Nationwide• Applied Medical Resources Corp 22872 Avenida Empresa # 3 Rancho Santa

Polaris Snowmobiles – Potential Mechanical Failure (2005)

Fire/Burn Risk

The recall involves all model year 2005 900 Fusion, 900 RMK, 900 Switchback snowmobiles, and select model year 2006 600HO Fusion / RMK / Switchback, 900 Fusion / RMK / Switchback, FS Classic / Touring, and FST Classic / Touring / Switchback snowmobiles. The model and serial number (VIN) identification decal is located on the right side of the tunnel underneath the seat. See affected model table below. Model Number of Affected Snowmobiles: Model Model Number 2005 900 Fusion S05MP8DS (A)(B)(C) 2005 900 RMK S05PL8DS (A)(B)(C)(D) S05PM8DS (A)(B) S05PN8DS S05PN8DE 2005 900 Switchback S05PS8DS 2006 600 HO Fusion S06MP6FS (A)(B) S06MC6FS S06ME6FS 2006 600 HO RMK S06PK6FS (A) 2006 600 HO Switchback S06PS6FS (A) 2006 900 Fusion S06MP8DS (A)(B) 2006 900 RMK S06PL8DS (A)(B) S06PM8DS (A) S06PN8DS (A) S06PR8DS 2006 900 Switchback S06PS8DS (A) 2006 FS Classic S06PD7ES 2006 FS Touring S06PT7ES 2006 FST Classic S06PD7FS 2006 FST Touring S06PT7FS 2006 FST Switchback S06PS7FS

CPSCOct 14, 2005Nationwide• Polaris Industries Inc., of Medina, Minn.

Dakocytomation California Inc: EnVision+, an ImmunoHistoChemistry reagent. This in-vitro...

This recall has been initiated due to a formulation error in the EnVision+ visualization reagent.

FDAOct 14, 2005Nationwide• Dakocytomation California Inc

Spacelabs Medical Incorporated: BirthNet OB Data Management System 91861

Potential for incorrect weight to be displayed.

FDAOct 13, 2005Nationwide• Spacelabs Medical Incorporated