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Boston Scientific Neuromodulation Corporation

Boston Scientific Neuromodulation Corporation Recalls

All product recalls associated with Boston Scientific Neuromodulation Corporation.

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Recall Summary

Total Recalls

1000

Past Year

566

Class I (Serious)

25

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 4061–4080 of 7756 recalls

Boston Scientific Neuromodulation Corporation: Fifty-five (55) cm 8 Contact Extension Kit, part number M...

The firm is initiating a voluntary removal of certain spinal cord stimulation leads, lead extensions, adapters, and deep brain stimulation lead extensions due to the "use by date" displayed on the label which is later than the correct "use by date". No adverse health consequence is expected to occur from this issue.

FDAApr 24, 2019Nationwide• Boston Scientific Neuromodulation Corporation

Boston Scientific Neuromodulation Corporation: LinearTM 3-4 50 cm 8 Contact Lead Kit, part number M365SC...

The firm is initiating a voluntary removal of certain spinal cord stimulation leads, lead extensions, adapters, and deep brain stimulation lead extensions due to the "use by date" displayed on the label which is later than the correct "use by date". No adverse health consequence is expected to occur from this issue.

FDAApr 24, 2019Nationwide• Boston Scientific Neuromodulation Corporation

Boston Scientific Neuromodulation Corporation: Precision TM M8 Adapter, 15 cm, part number M365SC9218150...

1...202 203204205 206...388

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The firm is initiating a voluntary removal of certain spinal cord stimulation leads, lead extensions, adapters, and deep brain stimulation lead extensions due to "use by date" displayed on the label which is later than the correct "use by date". No adverse health consequence is expected to occur from this issue.

FDAApr 24, 2019Nationwide• Boston Scientific Neuromodulation Corporation

Goldenseal Herb (AmeriHerb) – E. coli contamination (2019)

Dried spice and herb products potentially contaminated with generic E. coli.

Class IIModerate

FDAApr 24, 2019Nationwide• AmeriHerb International Inc

Lemon Balm Leaf (AmeriHerb) – E. coli contamination (2019)

Dried spice and herb products potentially contaminated with generic E. coli.

Class IIModerate

FDAApr 24, 2019Nationwide• AmeriHerb International Inc

Dill Weed (AmeriHerb) – E. coli contamination (2019)

Dried spice and herb products potentially contaminated with generic E. coli.

Class IIModerate

FDAApr 24, 2019Nationwide• AmeriHerb International Inc

Parsley Flakes (AmeriHerb) – E. coli contamination (2019)

Dried spice and herb products potentially contaminated with generic E. coli.

Class IIModerate

FDAApr 24, 2019Nationwide• AmeriHerb International Inc

Mullein Leaf (AmeriHerb) – E. coli contamination (2019)

Dried spice and herb products potentially contaminated with generic E. coli.

Class IIModerate

FDAApr 24, 2019Nationwide• AmeriHerb International Inc

Key Lime Cream Torte (Island Desserts) – undeclared colors (2019)

Undeclared Allergen

The product contains undeclared FD&C Colors Yellow #5 and Blue #1.

Class IIModerate

FDAApr 22, 2019MA, RI• Island Desserts Llc DBA Pastry Art

California Orange Blossom Honey (Glorybee) – unapproved antibiotic (2019)

Raw California Orange Blossom Honey was recalled due to two random FDA samples tested for unapproved fumagillin (antibiotic drug) residue.

FDAApr 19, 2019CA, CO, FL +7 more• Glorybee Natural Sweeteners, Inc.

Wooden Toy Vehicles (Target) – choking risk (2019)

This recall includes the Bullseye's Playground toy vehicles. The vehicles were sold individually in stores and as an 8-pack assortment online. The vehicles include a caboose, Santa in sleigh, ice cream truck/food truck, train, police car, fire truck, taxi, and digger. The item number, DPCI (model number), and UPC can all be found on a white sticker placed on the bottom of each vehicle. Item numbers included in the recall include: Name Item# DPCI (Model Number) UPC Caboose 89304 234-18-0100 765940893043 Santa in Sleigh 89297 234-18-0100 765940892978 Ice Cream Truck/Food Truck 89298 234-18-0100 765940892985 Train 89301 234-18-0100 765940893012 Police Car 89303 234-18-0100 765940893036 Firetruck 89302 234-18-0100 765940893029 Taxi 89300 234-18-0100 765940893005 Digger 89299 234-18-0100 765940892992 Toy Vehicles 8-Pack Assortment NA 234-20-0189 765940893159

CPSCApr 18, 2019Nationwide• Zhejiang HuangyanXingbo Crafts Factory, of China

Divalproex Sodium Tablets (Dr. Reddy's) – Humidity Exposure (2019)

cGMP deviations: Product was exposed above 50% relative humidity levels during packaging operations.

Class IIModerate

FDAApr 11, 2019Nationwide• Dr. Reddy's Laboratories, Inc.

Goji Powder (Xi'an Yuensun) – Fungicide Contamination (2019)

Fungicide carbendazim found in product.

FDAApr 8, 2019CA, FL, OH +1 more• Xi'an Yuensun Biological Technology Co., Ltd.

Hot/Cold Massage Balls (Vivitar) – Burn Hazard (2019)

This recall involves Vivitar Hot/Cold Massage Balls. The massage balls are teal, light pink or lavender and come in a package of two balls - one smooth ball and one with raised bumps. The name "Vivitar," model number, date code, and UPC can be found on the bottom of the product packaging. The date code can also be found on the smooth ball. Model Number Date Code UPC F19-MB-TL MID# 1940918 681066474037 F19-MB-LP MID# 1940918 681066305645 F19-MB-LV MID# 1940918 681066182475

CPSCApr 4, 2019Nationwide• Sakar International dba Vivitar, of Edison, N.J.

Pantoprazole Sodium Tablets (Jubilant Cadista) – Tablet Discoloration (2019)

Discoloration: Expansion of an earlier recall due to the presence of dark brown discoloration on the edges of the tablets.

Class IIModerate

FDAMar 29, 2019Nationwide• Jubilant Cadista Pharmaceuticals, Inc.

Home Elevators (Cambridge Elevating) – fall risk (2019)

This recall involves Cambridge Elevating Elmira, Heritage & Hybrid model home elevators using the first and second generation micro-controller systems (BES 1 & BES 2). "Cambridge Elevating" is printed on the label inside the elevators. The elevators have an operating panel inside the cab with a digital display, a stop button, the elevator capacity and a phone box. Only elevators with production date codes 1/2/2009 through 29/11/17 printed on the manufacture label inside the elevator wall are included in the recall.

CPSCMar 27, 2019Nationwide• Cambridge Elevating, of Cambridge, Ontario Canada

Thallous Chloride Injection (GE Healthcare) – Chemical Contamination (2019)

Chemical Contamination: Trace amounts of an impurity was detected in the reagent used to manufacture finished product.

FDAMar 26, 2019Nationwide• Medi-Physics Inc. dba GE Healthcare

2017 BFX FIRE APPARATUS BRUSH TRUCK Recall: EXTERIOR LIGHTING:BRAKE LIGHTS

SNF, Inc. dba BFX Fire Apparatus (BFX) is recalling certain 2017-2018 Brush Trucks equipped with Whelen brake lights recalled under 18E-063. Depending on the specific wiring of the vehicle, these brake lights may illuminate when the brake pedal has not been pressed.

NHTSAMar 25, 2019Nationwide• BFX FIRE APPARATUS

Biotin Injection (Auro Pharmacies) – pH Specification Failure (2019)

Failed pH Specification: product does not meet pH label claim.

FDAMar 22, 2019Nationwide• Auro Pharmacies Inc. DBA Central Drugs

Zero Turn Mowers (Kubota) – fire risk (2019)

This recall involves model years 2018 and 2019 Kubota ZD100 series gasoline-powered zero turn mowers. The model is printed on the side of the mowers. The data plate is located on the lower frame of the unit and contains the serial number and model number. Recalled units are orange and black. Model: Serial Number Range: Z122EBR-48 BEGIN END 21408 22007 Z121SKH-48 BEGIN END 31302 32882 Z125EBR-54 BEGIN END 16242 16547 Z125SKH-54 BEGIN END 29458 31138

CPSCMar 20, 2019Nationwide• Kubota Manufacturing of America Corporation, of Gainesville, Ga.