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Spagel Brothers, Inc.

Spagel Brothers, Inc. Recalls

All product recalls associated with Spagel Brothers, Inc..

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Recall Summary

Total Recalls

1000

Past Year

422

Class I (Serious)

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 2121–2140 of 4598 recalls

Pumpkin Cake Roll (Spagel Brothers) – mislabeling (2019)

Stanganellis Italian Foods, is initiating a recall of Pumpkin Cake Roll, Net Wt. 24 oz. . One per package, because of product miss-labeling. The firm inadvertently left off the allergen statement that soy was used in making the product.

Class IIModerate

FDAMar 26, 2019IN, PA• Spagel Brothers, Inc.

Testosterone Cypionate Injection (InvaGen) – Particulate Matter (2019)

Presence of Particulate Matter.

Class IIModerate

FDAMar 22, 2019Nationwide• InvaGen Pharmaceuticals, Inc.

Testosterone Cypionate Injection (InvaGen) – Particulate Matter (2019)

Presence of Particulate Matter.

Class II

1...105 106107108 109...230

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Moderate

FDAMar 22, 2019Nationwide• InvaGen Pharmaceuticals, Inc.

Testosterone Cypionate Injection (InvaGen) – Particulate Matter (2019)

Presence of Particulate Matter.

Class IIModerate

FDAMar 22, 2019Nationwide• InvaGen Pharmaceuticals, Inc.

2019 VOLKSWAGEN ATLAS Recall: AIR BAGS:SIDE/WINDOW

Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2019 Atlas and 2020 Passat vehicles. An incorrect driver and/or front passenger side impact air bag may have been installed.

NHTSAMar 20, 2019Nationwide• VOLKSWAGEN

2019 OSAGE SUPER WARRIOR Recall: EXTERIOR LIGHTING:BRAKE LIGHTS

Osage Industries, Inc. (Osage) is recalling certain 2015-2019 Osage Brave, Warrior and Super Warrior Type I and Type III ambulances equipped with Whelen brake lights. Depending on the specific wiring of the vehicle, these brake lights may illuminate when the brake pedal is not being pressed.

NHTSAMar 20, 2019Nationwide• OSAGE

Diclofenac Sodium Solution (Ingenus) – Leaking Bottles (2019)

Defective Container: firm discovered samples stored horizontally as well as product quality complaints from customers for bottles leaking.

Class IIILow

FDAMar 18, 2019Nationwide• Ingenus Pharmaceuticals Llc

Quinoa (Kroger) – pesticide contamination (2019)

Possible contamination with pesticide

Class IIILow

FDAMar 11, 2019CO, IN, KS +4 more• The Kroger Company

Mirapex Tablets (Boehringer) – Weight Specification Failure (2019)

Failed Tablet/Capsule Specifications: identification of low weight tablets during routine stability testing.

Class IIILow

FDAMar 7, 2019Nationwide• Boehringer Ingelheim Pharmaceuticals, Inc.

2018 VOLKSWAGEN TIGUAN Recall: SUSPENSION:REAR:SPRINGS:COIL SPRINGS

Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2017-2019 Golf Sportwagen, 2019 Jetta, 2015-2019 Golf, and 2018-2019 Tiguan vehicles. The rear coil springs may prematurely fracture.

NHTSAMar 6, 2019Nationwide• VOLKSWAGEN

2019 HIGHLAND RIDGE TT OPEN RANGE ULTRA LITE Recall: EQUIPMENT:OTHER:LABELS

Highland Ridge RV (Highland) is recalling certain 2019 Mesa Ridge Lite 2804RK and Open Range Ultra Lite 2804RK travel trailers. The Gross Vehicle Weight Rating (GVWR), shown on the label as 7,675lbs, exceeds the safety chain rating of 7,600lbs.

NHTSAMar 6, 2019Nationwide• HIGHLAND RIDGE TT

2019 VOLKSWAGEN JETTA Recall: AIR BAGS:FRONTAL

Volkswagen Group of America (Volkswagen) is recalling certain 2019 Jetta vehicles. An incorrect driver frontal airbag may have been installed during a service/repair visit.

NHTSAFeb 20, 2019Nationwide• VOLKSWAGEN

Temozolomide Capsules (Amerigen) – Failed Dissolution (2019)

Failed dissolution specifications

Class IIILow

FDAFeb 19, 2019Nationwide• Amerigen Pharmaceuticals Inc.

Etomidate Injection (Heritage) – Subpotent Drug (2019)

Subpotent Drug.

Class IIModerate

FDAFeb 15, 2019Nationwide• Heritage Pharmaceuticals, Inc.

PowerStream Sensor Power Supply (HK Anenerge) – Fire Hazard (2019)

Fire/Burn Risk

This recall involves power supply units sold with PurpleAir PA-II and PA-II- SD air quality sensors with model number RKPO-UL052000C. The model number is located on the bottom side of the power adapter. The power adapters are black with a white label. They measure 4 inches long (including the mounting tabs) by 1-7/8 inches wide by 1-3/8 inches high. The air quality sensors are used outdoors by consumers to monitor air quality.

CPSCFeb 14, 2019Nationwide• HK Anenerge Co., Ltd, of Guangdong Province, China

2019 VOLKSWAGEN BEETLE Recall: SERVICE BRAKES

Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2019 Beetle and Beetle Convertible vehicles. The instrument cluster may not provide a visual warning when a brake system failure is detected. As a result, the vehicles fail to comply with Federal Motor Vehicle Safety Standard (FMVSS) number 135, "Light vehicle brake systems" and number 101, "Controls and displays."

NHTSAFeb 13, 2019Nationwide• VOLKSWAGEN

VOYAGER VCMS140I REAR CAMERA Equipment Recall: EQUIPMENT

ASA Electronics, LLC. (ASA) is recalling certain Voyager monitors used to display the back-up camera image. The affected monitors may revert back to the factory default settings which may cause the camera image to be reversed.

NHTSAFeb 11, 2019Nationwide• VOYAGER

Unbleached All Purpose Flour (Gold Medal) – Salmonella Risk (2019)

Salmonella

Gold Medal Unbleached All Purpose 5 lb. flour is being recalled due to potential Salmonella contamination.

Class IIModerate

FDAJan 23, 2019AL, CO, CT +17 more• General Mills, Inc

2015 VOLKSWAGEN EOS Recall: AIR BAGS:FRONTAL:DRIVER SIDE:INFLATOR MODULE

Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2015 Passat, 2015-2016 Eos, 2015-2017 CC, 2016-2017 TT Roadster, TT Coupe, 2017 Audi R8 Coupe, and R8 Spyder vehicles. Upon deployment of the driver's frontal air bag, excessive internal pressure may cause the inflator to explode.

NHTSAJan 11, 2019Nationwide• VOLKSWAGEN

5K Premium Enhancement Capsules (Happy Together) – undeclared ingredients (2019)

Undeclared Allergen

Marketed without an Approved NDA/ANDA; FDA analysis found product to be tainted with undeclared sildenafil and tadalafil

Class IHigh

FDAJan 8, 2019Nationwide• Happy Together, Inc.