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Recall totals

All FDA and USDA recalls in Public Health Trace, June 2012 to September 2026.

37,142

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,799

Class I recallsReasonable probability of serious health consequences

24,349

Class II recallsTemporary or medically reversible health consequences

2,891

Class III recallsNot likely to cause adverse health consequences

Quick insights

A snapshot of the most notable patterns across all recorded FDA and USDA recalls.

Most recalled product100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in 150cc Amber Glass Packer with White Polypropylene Cap. 53 recalls

Most common hazardLack of Assurance of Sterility 2,072 recalls

Newest recallhttps://www.fsis.usda.gov/recalls-alerts/fontanini-foods-llc-recalls-raw-frozen-pork-sausage-products-due-possible-foreignPublished September 25, 2026

Most affected stateHawaii 200 recalls mention this state

State: SC ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated September 28, 2026 ET

Summary (Year to date)

1,527 recalls have been announced year to date.
Aug 2026 was 24% lower than the previous complete period (Jul 2026: 240).
The highest complete period was Jun 2026 (297).
Sep 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,349
Class I	9,799
Class III	2,891
Not Yet Classified	1

Recalls by class
Class	Recalls
Class II	24,349
Class I	9,799
Class III	2,891
Not Yet Classified	1

FDA Recall Terminated Historical recordClass II

Mirtazapine Tablets, USP 45 mg, a) 30 count, b) 100 count and c) 500 count bottles, Rx only, Mylan Pharmaceuticals Inc., Morgantown, WV

by Mylan Pharmaceuticals Inc.

Reason: Presence of Foreign Tablets/Capsules; possibility of Glipizide 10 mg tablet in bottle
Published: March 15, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Versa Marketing

Product: Fusia Asian Aspirations Szechuan Stir Fry; A delicious blen…
Reason: Product was tested and found positive for Listeria monocytogenes.
Published: March 15, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Trader Joes Company

Product: Trader Joes Imported English Authentic Lemon Curd, 10.5oz (…
Reason: Trader Joe's Co. is recalling the Lemon Curd because it contains undeclared milk in the sub-ingredient of butter.
Published: March 15, 2017
Distribution: US: CA, OR, AZ, WA, NV, NM, CO, UT, ID,…

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FDA Recall United States Terminated Historical recordClass II

Nu Skin Enterprises Inc.

Product: Pharmanex Cholestin. Cholesterol Health. 60 Softgels.
Reason: Nu Skin announces a voluntary field action for Pharmanex Cholestin due to undeclared allergen; soy.
Published: March 15, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Nu Skin Enterprises Inc.

Product: Pharmanex Cortitrol. Cortisol Management. 60 Capsules
Reason: Nu Skin announces a voluntary field action for Pharmanex Cortitrol due to undeclared allergen; soy.
Published: March 15, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Nu Skin Enterprises Inc.

Product: Pharmanex BioGinkgo. Mental Sharpness. 60 Tablets
Reason: Nu Skin announces a voluntary field action for Pharmanex BioGinkgo due to undeclared allergen; wheat.
Published: March 15, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

McCormick & Co Inc. Spice Mill Plant

Product: McCormick & Co., Inc., Stubbs Barbecue. 18oz Best By Date…
Reason: McCormick & Co., Inc., has decided to initiated a voluntary recall of there Stubbs Sticky Sweet BBQ Sauce 18oz Bottle. Best By Date of January 17, 2020. Because of a glass bottle defect. The glass defect involves various thickness and defects that may result in chipped or missing glass.
Published: March 15, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Robert Rothschild Farm LLC

Product: Gift Sets with Chocolate Pretzel Dippers
Reason: The product is not labeled with an ingredient statement and therefore, does not declare the allergens, soy and wheat.
Published: March 15, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Robert Rothschild Farm LLC

Product: Gift Sets with Pretzel Twists
Reason: The product is not labeled with an ingredient statement and therefore, does not declare the allergens, soy and wheat.
Published: March 15, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Hormel Foods Corporation

Product: Great Shake Plus Fortified Nutrition, Soy Formula, Strawberr…
Reason: Hormel Foods is recalling Great Shake and Great Shake Plus, fortified Nutrition drinks, due to presence of undeclared milk.
Published: March 15, 2017
Distribution: US: AL, CA, CO, CT, FL, GA, ID, IL, IN,…

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FDA Recall United States Terminated Historical recordClass II

Hormel Foods Corporation

Product: Great Shake Plus Fortified Nutrition, Soy Formula, Chocolate…
Reason: Hormel Foods is recalling Great Shake and Great Shake Plus, fortified Nutrition drinks, due to presence of undeclared milk.
Published: March 15, 2017
Distribution: US: AL, CA, CO, CT, FL, GA, ID, IL, IN,…

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FDA Recall United States Terminated Historical recordClass II

Hormel Foods Corporation

Product: Great Shake Plus Fortified Nutrition, Soy Formula, Vanilla A…
Reason: Hormel Foods is recalling Great Shake and Great Shake Plus, fortified Nutrition drinks, due to presence of undeclared milk.
Published: March 15, 2017
Distribution: US: AL, CA, CO, CT, FL, GA, ID, IL, IN,…

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FDA Recall United States Terminated Historical recordClass II

Hormel Foods Corporation

Product: Great Shake Fortified Nutrition, Soy Formula, Vanilla Artifi…
Reason: Hormel Foods is recalling Great Shake and Great Shake Plus, fortified Nutrition drinks, due to presence of undeclared milk.
Published: March 15, 2017
Distribution: US: AL, CA, CO, CT, FL, GA, ID, IL, IN,…

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FDA Recall United States Terminated Historical recordClass II

Hormel Foods Corporation

Product: Great Shake Fortified Nutrition, Soy Formula, Strawberry Art…
Reason: Hormel Foods is recalling Great Shake and Great Shake Plus, fortified Nutrition drinks, due to presence of undeclared milk.
Published: March 15, 2017
Distribution: US: AL, CA, CO, CT, FL, GA, ID, IL, IN,…

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FDA Recall United States Terminated Historical recordClass II

Hormel Foods Corporation

Product: Great Shake Fortified Nutrition, Soy Formula, Chocolate Arti…
Reason: Hormel Foods is recalling Great Shake and Great Shake Plus, fortified Nutrition drinks, due to presence of undeclared milk.
Published: March 15, 2017
Distribution: US: AL, CA, CO, CT, FL, GA, ID, IL, IN,…

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FDA Recall United States Terminated Historical recordClass II

Legendary Baking

Product: Private Selection, Salted Caramel Chocolate Almond Pie, NET…
Reason: Salted Carmel Chocolate Almond Pie was mislabeled. The wrong ingredient label was used which did not listed two allergens, eggs and almonds.
Published: March 15, 2017
Distribution: DISTRIBUTION CENTERS: OR, OH, CO, KY, AZ…

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FDA Recall United States Terminated Historical recordClass I

NSE Products, Inc.

Product: Pharmanex ageLOC TR90 Protein Boost. Protein Powder. Net wt.…
Reason: Nu Skin announces a voluntary field action for Pharmanex ageLOC TR90 Protein Boost due to an undeclared milk allergen.
Published: March 15, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Zenatane (isotretinoin) capsules, 10 mg, packaged in 30-count cartons (3 x 10 blister cards), Rx Only, Manufactured By:Cipla Limited Kurkumbh Village Pune 413802 India, Manufactured For: Dr. Reddy's Laboratories, Bachupally 500 090 India, NDC 55111-135-81

by Dr. Reddy's Laboratories, Inc.

Reason: Failed dissolution specifications - low dissolution results at S3 stage.
Published: March 8, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Zenatane (isotretinoin) capsules, 30 mg, packaged in 30-count cartons (3 x 10 blister cards), Rx Only, Manufactured By:Cipla Limited Kurkumbh Village Pune 413802 India, Manufactured For: Dr. Reddy's Laboratories, Bachupally 500 090 India, NDC 5511-113-81

by Dr. Reddy's Laboratories, Inc.

Reason: Failed dissolution specifications - low dissolution results at S3 stage.
Published: March 8, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Zenatane (isotretinoin) capsules, 20 mg, packaged in 30-count cartons (3 x 10 blister cards), Rx Only, Manufactured By:Cipla Limited Kurkumbh Village Pune 413802 India, Manufactured For: Dr. Reddy's Laboratories, Bachupally 500 090 India, NDC 55111-136-81

by Dr. Reddy's Laboratories, Inc.

Reason: Failed dissolution specifications - low dissolution results at S3 stage.
Published: March 8, 2017
Distribution: Nationwide

View recall →

Data last updated: September 28, 2026 ET

Recall records are summarized from official FDA and USDA sources. Notices may be updated, reclassified, terminated, or withdrawn. Always review the linked official notice for the most current instructions. Read the full medical disclaimer.