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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 10,641–10,660 of 19,095 recalls

FDA Recall Terminated Historical recordClass II

Thyroid, USP (Porcine) Levothyroxine 36.3 mcg/grain Liothyronine 9.7 mcg/grain Active Pharmaceutical Ingredient Rx Only 1000 grams NDC 0395-8077-43 Packaged by: Humco Texarkana, TX 75501

by Humco Holding Group, Inc

Reason
CGMP Deviations: Recall notice received from supplier that Thyroid Powder has inconsistent levels of the active ingredients levothyroxine and liothyronine.
Published
October 24, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

La Mexicana LLC

Product
La Mexicana (Pico with) Guacamole 10 oz..
Reason
Potential Listeria monocytogenes contamination.
Published
October 24, 2018
Distribution
U.S. distribution to the following: CA,…

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FDA Recall United States Terminated Historical recordClass I

La Mexicana LLC

Product
La Mexicana Cantina Salsa 14 oz., 24 oz., and 64 oz.
Reason
Potential Listeria monocytogenes contamination.
Published
October 24, 2018
Distribution
U.S. distribution to the following: CA,…

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FDA Recall United States Terminated Historical recordClass I

La Mexicana LLC

Product
La Mexicana Garlic Salsa 16 oz. Gourmet Style Garlic 16 oz.
Reason
Potential Listeria monocytogenes contamination.
Published
October 24, 2018
Distribution
U.S. distribution to the following: CA,…

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FDA Recall United States Terminated Historical recordClass I

La Mexicana LLC

Product
La Mexicana Peach Mango Salsa 16 oz., 24 oz., and 64 oz.
Reason
Potential Listeria monocytogenes contamination.
Published
October 24, 2018
Distribution
U.S. distribution to the following: CA,…

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FDA Recall United States Terminated Historical recordClass I

La Mexicana LLC

Product
La Mexicana Medium Salsa 16 oz., 24 oz., 48 oz., 64 oz., and…
Reason
Potential Listeria monocytogenes contamination.
Published
October 24, 2018
Distribution
U.S. distribution to the following: CA,…

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FDA Recall United States Terminated Historical recordClass I

La Mexicana LLC

Product
La Mexicana Mild Salsa 16 oz., 24 oz., 48 oz., 64 oz., and 1…
Reason
Potential Listeria monocytogenes contamination.
Published
October 24, 2018
Distribution
U.S. distribution to the following: CA,…

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FDA Recall United States Terminated Historical recordClass I

La Mexicana LLC

Product
La Mexicana Hot Salsa 16 oz., 24 oz., 48 oz., 64 oz., and 12…
Reason
Potential Listeria monocytogenes contamination.
Published
October 24, 2018
Distribution
U.S. distribution to the following: CA,…

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FDA Recall United States Terminated Historical recordClass II

Tarry Medical Products, Inc.

Product
Product comes in a plastic bag which is labeled as follows:…
Reason
Microorganism found inside vial.
Published
October 24, 2018
Distribution
Direct to PA, WI, OH, GA, NE, CA

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FDA Recall United States Terminated Historical recordClass II

Iowa Choice Harvest, LLC.

Product
Sweet corn, Net weight 20 pounds, Marshalltown IA
Reason
Sample analysis of frozen corn detected the presence of fecal coliform bacteria and generic E. coli.
Published
October 24, 2018
Distribution
Distributed to customers in Iowa and Neb…

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FDA Recall Terminated Historical recordClass II

Prevacid 24HR (Lansoprazole) delayed-release capsules, 15 mg, 14 capsules per bottle in a carton containing 1 bottle (NDC: 0067-6286-14), 2 bottles (NDC: 0067-6286-28) or 3 bottles (NDC: 0067-6286-42), Over-the-counter, Distributed By: GSK Consumer Healthcare, Warren, NJ 07059.

by GLAXOSMITHKLINE NEBRASKA

Reason
CGMP deviations
Published
October 17, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Altavera Levonorgestrel and Ethinyl Estradiol Tablets, USP 0.15 mg and 0.03 mg, Rx only, 3 tablet dispensers x 28 tablets. Manufactured by Laboratories Leon Farma S.A., Spain, for Xiromed, LLC., Florham Park, NJ 07932. Product of Spain NDC 70700-116-85 (I unit x 28 tablets 70700-116-84)

by Xiromed LLC

Reason
Labeling: Not Elsewhere Classified: mislabeling of the Altavera generic name on the packaging component that may cause confusion.
Published
October 17, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Magnesium Sulfate in Water for Injection (0.325 mEq Mg++/mL) 40 mg/mL, 20 g Total, 500 mL Single-Dose Container bag, Rx only, Hospira, Inc. Lake Forest, IL 60045 USA, NDC 0409-6729-03.

by Pfizer Inc.

Reason
Correct Labeled Product Mispack: confirmed report involving a single unit of properly labeled Heparin in 0.45% Sodium Chloride for Injection (NDC 0409-7651-03, Lot 87903FW) that was found inside a case of Magnesium Sulfate in Water for Injection.
Published
October 17, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Amlodipine Besylate USP 10 mg Tablets, 1000-count bottles, Rx Only, Manufactured by: Cipla Ltd., Verna Goa, India, Manufactured for: Cipla USA, Inc. 1560 Sawgrass Corporate Parkway, Suite 130, Sunrise FL 33323 UPC 369097128159, NDC 69097-128-15

by InvaGen Pharmaceuticals, Inc.

Reason
Subpotent Drug: One lot of product does not meet the product specification for Assay test at 3 month long term stability condition.
Published
October 17, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Pantoprazole Sodium Delayed-Release Tablets, USP, 40 mg*, 90-count bottle, Rx only, Manufactured by: Jubilant Generics Ltd., Roorkee - 247661, India; Marketed by: Jubilant Cadista Pharmaceuticals Inc., Salisbury, MD 21801; NDC 59746-284-90.

by Jubilant Cadista Pharmaceuticals, Inc.

Reason
Discoloration: Presence of dark discoloration or brown spots on the edges of the tablets.
Published
October 17, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Glipizide XL (glipizide) extended-release tablets 5 mg 500-tablet bottle, Rx only Distributed by: Greenstone LLC. Peapack, NJ 07977 --- NDC 59762-0541-2

by Pfizer Inc.

Reason
CGMP Deviations; rejected product was used to manufacture final bulk lot
Published
October 17, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Sarap Asian Fusion

Product
Ube Cookies & Cream (cookies); A Sarap Asian Fusion Product…
Reason
Undeclared wheat, soy lecithin, and milk
Published
October 17, 2018
Distribution
Online to customers in AE, AK, AL, AR, A…

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FDA Recall United States Terminated Historical recordClass II

Sarap Asian Fusion

Product
Matcha Chocolate (cookies); A Sarap Asian Fusion Product;…
Reason
Undeclared wheat and soy lecithin
Published
October 17, 2018
Distribution
Online to customers in AE, AK, AL, AR, A…

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FDA Recall United States Terminated Historical recordClass II

Sarap Asian Fusion

Product
Black Sesame White Chocolate (cookies); A Sarap Asian Fusio…
Reason
Undeclared wheat, soy lecithin, and milk
Published
October 17, 2018
Distribution
Online to customers in AE, AK, AL, AR, A…

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FDA Recall United States Terminated Historical recordClass II

Sarap Asian Fusion

Product
Miso Milo Chocolate (cookies); A Sarap Asian Fusion Product…
Reason
Undeclared wheat and soy lecithin
Published
October 17, 2018
Distribution
Online to customers in AE, AK, AL, AR, A…

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.