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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.

37,066
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,786
Class I recallsReasonable probability of serious health consequences
24,313
Class II recallsTemporary or medically reversible health consequences
2,876
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
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 II24,313
Class I9,786
Class III2,876
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,313
Class I9,786
Class III2,876
Not Yet Classified2

Showing 3,501–3,520 of 21,007 recalls

FDA Recall United States Terminated Historical recordClass II

Conopco DBA Unilever

Product
Knorr Letras con Tomate Tomato Based Alphabet Pasta Soup Mix…
Reason
Undeclared egg
Published
September 20, 2023
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Conopco DBA Unilever

Product
Knorr Fideos con Tomate Tomato Based Pasta Soup Mix 3.5 oz U…
Reason
Undeclared egg
Published
September 20, 2023
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Conopco DBA Unilever

Product
Knorr Estrellitas con Tomate Tomato Based Star Pasta Soup Mi…
Reason
Undeclared egg
Published
September 20, 2023
Distribution
Nationwide

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FDA Recall United States Ongoing Historical recordClass II

Twin City Foods, Inc.

Product
Mixed Vegetables BEST PRICE TOPVALU, net per bag 500g. Label…
Reason
Listeria monocytogenes
Published
September 20, 2023
Distribution
Nationwide

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FDA Recall United States Ongoing Historical recordClass II

Twin City Foods, Inc.

Product
Kernel Corn, BEST PRICE TOPVALU, net wt. per bag 300g. Label…
Reason
Listeria monocytogenes
Published
September 20, 2023
Distribution
Nationwide

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FDA Recall United States Ongoing Historical recordClass II

Twin City Foods, Inc.

Product
Individually Quick Frozen (IQF) Corn, distributed in bulk ca…
Reason
Listeria monocytogenes
Published
September 20, 2023
Distribution
Nationwide

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FDA Recall United States Ongoing Historical recordClass II

Twin City Foods, Inc.

Product
Individually Quick Frozen (IQF) Corn distributed in BULK TOT…
Reason
Listeria monocytogenes
Published
September 20, 2023
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Chemtrade Solutions, LLC

Product
Sodium Nitrite, Granular Super Free-Flowing Food Grade, 50lb…
Reason
Product may contain metal fragments (ferrous metal, 1 mm or less in size)
Published
September 20, 2023
Distribution
IA, IL, MI, TX, WI and Mexico

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FDA Recall United States Terminated Historical recordClass III

Twin Cities Co-Op Partners Inc.

Product
La Reyna Queso Dip. Product Code 1781. Net Wt 16 oz. UPC…
Reason
Dips and sauces received out of temperature specifications. Product was not quarantined; product was shipped to customers.
Published
September 20, 2023
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass III

Twin Cities Co-Op Partners Inc.

Product
La Reyna Salsa Roja, Gluten Free / Medium. Product Code 178…
Reason
Dips and sauces received out of temperature specifications. Product was not quarantined; product was shipped to customers.
Published
September 20, 2023
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass III

Twin Cities Co-Op Partners Inc.

Product
La Reyna Guacamole, Gluten Free. Product Code 1780. Net Wt…
Reason
Dips and sauces received out of temperature specifications. Product was not quarantined; product was shipped to customers.
Published
September 20, 2023
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass III

Twin Cities Co-Op Partners Inc.

Product
La Reyna Salsa Verde, Gluten Free / Medium. Product Code 17…
Reason
Dips and sauces received out of temperature specifications. Product was not quarantined; product was shipped to customers.
Published
September 20, 2023
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass III

Twin Cities Co-Op Partners Inc.

Product
La Reyna Diablo Salsa. Red Diablo Salsa, Hot. Product Code…
Reason
Dips and sauces received out of temperature specifications. Product was not quarantined; product was shipped to customers.
Published
September 20, 2023
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

David Oppenheimer & Company I LLC

Product
Zespri Organic Green Kiwi, product of New Zealand, one palle…
Reason
Listeria monocytogenes
Published
September 20, 2023
Distribution
Distributed in FL, GA, IL, IN, KY, MI, N…

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FDA Recall United States Terminated Historical recordClass I

David Oppenheimer & Company I LLC

Product
Zespri Organic Green Kiwi, product of New Zealand, perishabl…
Reason
Listeria monocytogenes
Published
September 20, 2023
Distribution
Distributed in FL, GA, IL, IN, KY, MI, N…

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FDA Recall Terminated Historical recordClass II

Digoxin Tablets, USP 0.25mg, 100-count bottles, Rx Only, Manufactured for/Distributed by: Marlex Pharmaceuticals, Inc. New Castle, DE NDC 10135-0748-01

by Marlex Pharmaceuticals, Inc.

Reason
Labeling: Label Mix-Up- Bottles labeled as Digoxin Tablets, USP 0.125 mg contain Digoxin Tablets, USP 0.25mg and bottles labeled as Digoxin Tablets, USP 0.25mg contain Digoxin Tablets, USP 0.125mg.
Published
September 13, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

Digoxin Tablets, USP 0.125mg, 100-count bottles, Rx Only, Manufactured for/Distributed by: Marlex Pharmaceuticals, Inc. New Castle, DE NDC# 10135-0747-01

by Marlex Pharmaceuticals, Inc.

Reason
Labeling: Label Mix-Up- Bottles labeled as Digoxin Tablets, USP 0.125 mg contain Digoxin Tablets, USP 0.25mg and bottles labeled as Digoxin Tablets, USP 0.25mg contain Digoxin Tablets, USP 0.125mg.
Published
September 13, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Fosfomycin Tromethamine Granules for Oral Solution, 3 g single- dose sachet, Rx only, Manufactured by: Alkem Laboratories Ltd., INDIA, Distributed by: Ascend Laboratories, LLC, Parsippany, NJ 07054, NDC# 67877-749-57

by Ascend Laboratories, LLC

Reason
Failed Impurities/Degradation Specifications: Out-of-specification results observed for the organic impurities test at 6 months, RT Stability.
Published
September 13, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Milrinone Lactate Injection, USP 20mg/20 mL (1mg/mL), packaged in 10 x 20 mL vials per carton, NDC 72485-502-01 (single vial), Rx only, Distributed by: Armas Pharmaceuticals, Inc. Freehold, NJ 07728(USA) Manufactured by: Caplin Steriles Limited, India, NDC 72485-502-10

by Caplin Steriles Limited

Reason
Failed Impurities/Degradation Specifications
Published
September 13, 2023
Distribution
Nationwide

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FDA Recall Completed Historical recordClass III

Nexlizet (bempedoic acid and ezetimibe), 180ng/18mg, 30 tablets, Rx only, Manufactured for: Esperion Therapeutics, Inc, Ann Arbor, MI 48108, NDC 72426-818-03

by Esperion

Reason
Failed dissolution specifications: below specification results at stability 12-month
Published
September 13, 2023
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.