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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 4,021–4,040 of 21,105 recalls

FDA Recall Terminated Historical recordClass II

Microplegia (MSA/MSG 0.92 Molar) packaged in 125 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0001-1.

by Central Admixture Pharmacy Services, Inc.

Reason
Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.
Published
May 31, 2023
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Albertsons Companies LLC

Product
Oatmeal Raisin Cookies 18 Count, Safeway brand, packaged in…
Reason
Undeclared peanut and soy.
Published
May 31, 2023
Distribution
distributed in WA.

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FDA Recall United States Terminated Historical recordClass II

Pernod Ricard Usa Inc

Product
Copitas; small ceramic cups; "Del Maguey" embossed on the bo…
Reason
Product may exceed FDA guidance levels for leachable lead.
Published
May 31, 2023
Distribution
Alabama, Arkansas, Arizona, California,…

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FDA Recall United States Ongoing Historical recordClass II

TruVision Health LLC

Product
TruBoost Drink - Ruby Rev
Reason
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
Published
May 31, 2023
Distribution
Alabama Alaska Arizona Arkansas Californ…

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FDA Recall United States Ongoing Historical recordClass II

TruVision Health LLC

Product
TruBoost Drink - Citrine Spark
Reason
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
Published
May 31, 2023
Distribution
Alabama Alaska Arizona Arkansas Californ…

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FDA Recall United States Ongoing Historical recordClass II

TruVision Health LLC

Product
TruBoost 7 Day Experience Kit
Reason
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
Published
May 31, 2023
Distribution
Alabama Alaska Arizona Arkansas Californ…

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FDA Recall United States Ongoing Historical recordClass II

TruVision Health LLC

Product
Truvy Boost 30-Day Experience Kit
Reason
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
Published
May 31, 2023
Distribution
Alabama Alaska Arizona Arkansas Californ…

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FDA Recall United States Ongoing Historical recordClass II

TruVision Health LLC

Product
Truvy 7-Day Experience Kit
Reason
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
Published
May 31, 2023
Distribution
Alabama Alaska Arizona Arkansas Californ…

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FDA Recall United States Ongoing Historical recordClass II

TruVision Health LLC

Product
Truvy 30-Day Experience Kit
Reason
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
Published
May 31, 2023
Distribution
Alabama Alaska Arizona Arkansas Californ…

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FDA Recall United States Ongoing Historical recordClass II

TruVision Health LLC

Product
TruWeight and Energy Gen 2+ Trifold
Reason
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
Published
May 31, 2023
Distribution
Alabama Alaska Arizona Arkansas Californ…

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FDA Recall United States Ongoing Historical recordClass II

TruVision Health LLC

Product
TruWeight and Energy Gen 2+ 60 Count
Reason
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
Published
May 31, 2023
Distribution
Alabama Alaska Arizona Arkansas Californ…

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FDA Recall United States Ongoing Historical recordClass II

TruVision Health LLC

Product
truControl W/Dynamine 60 ct
Reason
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
Published
May 31, 2023
Distribution
Alabama Alaska Arizona Arkansas Californ…

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FDA Recall United States Ongoing Historical recordClass II

TruVision Health LLC

Product
reFORM
Reason
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
Published
May 31, 2023
Distribution
Alabama Alaska Arizona Arkansas Californ…

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FDA Recall United States Ongoing Historical recordClass II

TruVision Health LLC

Product
TruControl 7 Day Trifold
Reason
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
Published
May 31, 2023
Distribution
Alabama Alaska Arizona Arkansas Californ…

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FDA Recall United States Ongoing Historical recordClass II

TruVision Health LLC

Product
truCONTROL 60 Count
Reason
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
Published
May 31, 2023
Distribution
Alabama Alaska Arizona Arkansas Californ…

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FDA Recall United States Terminated Historical recordClass II

Julie's Real Foods LLC

Product
Julie's Real JR Bar Dark Chocolate Grain-Free Granola Bar, N…
Reason
Possible presence of foreign material (metal)
Published
May 31, 2023
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Julie's Real Foods LLC

Product
Julie's Real JR Bar Cinnamon Vanilla Bean Grain-Free Granola…
Reason
Possible presence of foreign material (metal)
Published
May 31, 2023
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Hms Host International Inc

Product
House Made Tarragon Chicken Salad Sandwich, brand DishD'Lish…
Reason
Tarragon Chicken Salad Sandwich label declares Mayonnaise and Bread, but label does NOT declare Egg and Wheat.
Published
May 31, 2023
Distribution
distributed in WA.

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FDA Recall United States Terminated Historical recordClass I

Hms Host International Inc

Product
Ultra Tuna Salad Sandwich, brand DishD'Lish. The label decl…
Reason
Ultra Tuna Salad Sandwich label declares Mayo and Bread, but label does NOT declare Egg and Wheat.
Published
May 31, 2023
Distribution
distributed in WA.

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FDA Recall United States Terminated Historical recordClass I

Hms Host International Inc

Product
Ultra Tuna Salad Cup, brand DishD'Lish, packaged in plastic…
Reason
Ultra Tuna Salad in a Cup label does not declare egg.
Published
May 31, 2023
Distribution
distributed in WA.

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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.