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McCormick & Company, Inc. - Flavor Manufacturing Center

McCormick & Company, Inc. - Flavor Manufacturing Center Recalls

All product recalls associated with McCormick & Company, Inc. - Flavor Manufacturing Center.

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Recall Summary

Total Recalls

1000

Past Year

726

Class I (Serious)

175

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 4881–4900 of 11124 recalls

Meijer Taco Seasoning (McCormick) – undeclared milk (2018)

Undeclared Milk

Product contains undeclared milk.

Class IHigh

FDASep 10, 2018Nationwide• McCormick & Company, Inc. - Flavor Manufacturing Center

Sesame Noodle Salad Vegan (Market of Choice) – undeclared egg (2018)

Undeclared Egg

Sesame Noodle Salad Vegan is recalled due to undeclared egg.

Class IHigh

FDASep 7, 2018IN, OR• Market of Choice Inc

Thyroid Powder (Alkano Chemicals) – Ingredient Inconsistency (2018)

CGMP Deviations: Recall notice received from supplier that Thyroid Powder has inconsistent levels of the active ingredients levothyroxine and liothyronine.

1...243 244245246 247...557

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Class IIModerate

FDAAug 30, 2018IN, MN• Alkano Chemicals, Inc

CedarLane Organic Salads (Cedarlane) – Undeclared Wheat (2018)

Discovery that the product is labeled as gluten free but contains wheat (couscous). Wheat is not declared as an allergen

Class IIModerate

FDAAug 29, 2018CA, CO, FL +7 more• Cedarlane Natural Foods Inc/Frankly Fresh Foods Inc.

Ethosuximide Capsules (Akorn) – Impurity Specification (2018)

Failed Impurities/Degradation Specifications: Out of specification (OOS) results for unspecified impurity.

Class IIModerate

FDAAug 24, 2018Nationwide• Akorn, Inc.

Amlodipine Valsartan HCTZ (RemedyRepack) – Trace Contaminant (2018)

CGMP Deviations: Detection of trace amounts of NDMA, a possible impurity or contaminant in an active pharmaceutical ingredient.

Class IIModerate

FDAAug 24, 2018IN, SC• RemedyRepack Inc.

Dewey's Chocolate Brownie Cookies – Mold Contamination (2018)

The firm was notified by a customer that mold was in the product.

Class IIModerate

FDAAug 23, 2018AZ, AR, CA +24 more• Dewey's Bakery, Inc dba Salem Baking Company

Kenworth W900 (Kenworth) – Wiring Harness Issue (2018)

PACCAR Incorporated (PACCAR) is recalling certain 2016-2019 Kenworth C500, T660, T800, and W900 vehicles, equipped with 1.9M ISX15 engines. The engine harnesses may have been manufactured without check engine light (CEL) and stop engine light (SEL) circuits, preventing the driver from being warned of a serious engine problem.

High

NHTSAAug 22, 2018Nationwide• KENWORTH

Volkswagen Atlas (Volkswagen) – Airbag Control Module (2018)

Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2018 Volkswagen Atlas vehicles. During production, the air conditioning system drain tube may have been twisted, causing water to drain into the air bag control module.

High

NHTSAAug 20, 2018Nationwide• VOLKSWAGEN

Amlodipine/Valsartan/HCTZ Tablet (RemedyRepack) – potential contaminant (2018)

CGMP Deviations: Detection of trace amounts of NDMA, a possible impurity or contaminant in an active pharmaceutical ingredient.

Class IIModerate

FDAAug 20, 2018SC• RemedyRepack Inc.

Volkswagen Passat (Volkswagen) – Brake Caliper Issue (2018)

Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2018 Volkswagen Atlas and 2017-2018 Volkswagen Passat vehicles. The brake caliper bracket mounting bolts on these vehicles may not have been tightened sufficiently.

High

NHTSAAug 15, 2018Nationwide• VOLKSWAGEN

WorkSafe 3-D Cell Flashlights (Koehler-Bright Star) – Explosion Hazard (2018)

This recall involvesWorkSafe 3-D cell flashlights, model number 2224 LED. The model number is printed at the top right side of the text contained on the flashlight. The flashlight is safety orange with a black reflector assembly and black end cap and measures about 10.25 inches long by 2 inches in diameter. Only 3-D cell flashlights that do not contain a date code stamped on the body of the units are included in the recall

High

CPSCAug 14, 2018Nationwide• Koehler-Bright Star, of Hanover, Pa.

Valsartan Tablets (AVKARE) – Carcinogen Impurity (2018)

CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.

Class IIModerate

FDAAug 14, 2018Nationwide• AVKARE Inc.

Megestrol Acetate Suspension (Mckesson) – Subpotent Drug (2018)

Supterpotent Drug

Class IIModerate

FDAAug 14, 2018Nationwide• Mckesson Corporation

Valsartan Tablets (AVKARE) – Carcinogen Impurity (2018)

CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.

Class IIModerate

FDAAug 14, 2018Nationwide• AVKARE Inc.

Valsartan Tablets (AVKARE) – Carcinogen Impurity (2018)

CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.

Class IIModerate

FDAAug 14, 2018Nationwide• AVKARE Inc.

Valsartan Tablets (AVKARE) – Carcinogen Impurity (2018)

CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.

Class IIModerate

FDAAug 14, 2018Nationwide• AVKARE Inc.

Valsartan Tablets (RemedyRepack) – Carcinogen Impurity (2018)

CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.

Class IIModerate

FDAAug 10, 2018FL, IN, VA• RemedyRepack Inc.

Valsartan Tablets (RemedyRepack) – Carcinogen Impurity (2018)

CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.

Class IIModerate

FDAAug 10, 2018FL, IN, VA• RemedyRepack Inc.

Valsartan Tablets (RemedyRepack) – Carcinogen Impurity (2018)

CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.

Class IIModerate

FDAAug 10, 2018FL, IN, VA• RemedyRepack Inc.