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Research historical outbreak investigations and the full recall archive, with charts, trends, and advanced filters. Looking for what's happening right now instead? See current Health Alerts.

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

Download matching recalls as CSV

CSV exports include up to 5,000 matching rows (applying your current filters), not the full dataset if it's larger.

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Recalls announced by month (Year to date)

A chart of recalls grouped by month.

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Source: FDA and USDA public dataLast updated

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

A bar chart of the total number of recalls in this dataset by recall class.

Recalls by class
ClassRecalls
Class II24,349
Class I9,799
Class III2,891
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,349
Class I9,799
Class III2,891
Not Yet Classified1

Showing 12,981–13,000 of 18,726 recalls

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 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

View recall →

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

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FDA Recall Terminated Historical recordClass III

Zenatane (isotretinoin) capsules, 40 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 55111-137-81

by Dr. Reddy's Laboratories, Inc.

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

View recall →

FDA Recall Terminated Historical recordClass I

Nano PNC Water, packaged in amber glass bottles, Rx only, ICRPstudy.com, Immune Cellular Restoration Program.

by Pacific Medical Solutions

Reason
Marketed without an Approved NDA/ANDA and non-sterility: NANO PNC Water by nebulizer was sampled and found to contain variovorax paradoxus.
Published
March 8, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Salicylic Acid Cream, 6%, 400g bottle, Rx Only, Manufactured By Perrigo Yeruham, Israel 80500, Distributed By Perrigo Allegan, MI 49010, NDC 45802-806-01, UPC 3 45802-806-01 7.

by L. Perrigo Company

Reason
Failed Impurities/Degradation Specifications: The API for these products had an out of specification result for an organic impurity.
Published
March 8, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Salicylic Acid Shampoo, 6%, 177 mL bottle, Rx only, Manufactured By Perrigo Yeruham, Israel, Distributed By Perrigo Allegan, MI 49010, NDC 45802-237-01, UPC 3 45802-237-01 9.

by L. Perrigo Company

Reason
Failed Impurities/Degradation Specifications: The API for these products had an out of specification result for an organic impurity.
Published
March 8, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Alfuzosin Hydrochloride Extended-release Tablets, 10 mg, 100-count bottles, Rx only, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512; Manufactured by: Sun Pharmaceutical Ind. Ltd., Halol-Baroda Highway, Halol-389, Gujarat, India, NDC 47335-956-88.

by Sun Pharmaceutical Industries, Inc.

Reason
Presence of Foreign Substance: consumer complaint for foreign matter embedded in the tablet identified as a broken piece of wire rope from the manufacturing equipment.
Published
March 8, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

HealthA2Z CHEWABLE Aspirin (NSAID) 81 mg, Orange Flavor, 36 Chewable Tablets, a) packaged in 36-count bottle [UPC Code 369168288362 (FP0545)], b) bulk product (6K28817), OTC, Manufactured by: Allegiant Health Deer Park, NY 11729

by Allegiant Health

Reason
cGMP deviations - presence of rubber particles found loose in the bulk product.
Published
March 8, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

EYE WASH, 4 fl oz. (118 mL) bottle, OTC, Distributed by: Major Pharmaceutical, 31778 Enterprise Drive, Livonia, MI 48150, Made in Korea, NDC 0904-6491-20

by United Exchange Corporation

Reason
Lack of assurance of sterility
Published
March 8, 2017
Distribution
Nationwide

View recall →

Data last updated:

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.