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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 October 2026.

37,324
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,859
Class I recallsReasonable probability of serious health consequences
24,440
Class II recallsTemporary or medically reversible health consequences
2,900
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 2,095 recalls
Newest recallhttps://www.fsis.usda.gov/recalls-alerts/kayem-foods-inc--recalls-meat-and-poultry-products-due-possible-temperature-abusePublished October 17, 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)

  • 1,739 recalls have been announced year to date.
  • Sep 2026 was 15% higher than the previous complete period (Aug 2026: 182).
  • The highest complete period was Jun 2026 (300).
  • Oct 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 II24,440
Class I9,859
Class III2,900
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,440
Class I9,859
Class III2,900
Not Yet Classified2

Showing 4,041–4,060 of 19,414 recalls

FDA Recall TerminatedTerminated: June 22, 2025Historical 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 OngoingHistorical 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 OngoingHistorical 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 OngoingHistorical 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 OngoingHistorical 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…

View recall →

FDA Recall United States OngoingHistorical 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…

View recall →

FDA Recall United States OngoingHistorical 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 OngoingHistorical 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 OngoingHistorical 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 OngoingHistorical 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 OngoingHistorical 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 OngoingHistorical 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…

View recall →

FDA Recall United States OngoingHistorical 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 TerminatedTerminated: April 18, 2024Historical 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 TerminatedTerminated: April 18, 2024Historical 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 TerminatedTerminated: March 22, 2024Historical recordClass II

Kawasho Foods USA, Inc

Product
Geisha Medium Shrimp; WT 4OZ(113g)
Reason
Canned shrimp may be under-processed
Published
May 31, 2023
Distribution
Nationwide

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FDA Recall TerminatedTerminated: April 5, 2024Historical recordClass II

Piperacillin and Tazobactam for Injection, UPS, 3.375 grams per vial, Rx only, Manufactured for: Xellia Pharmaceuticals USA, LLC, Buffalo Grove, IL 60089, NDC 70594-079-02

by Astral SteriTech Private Ltd.

Reason
Lack of Assurance of Sterility
Published
May 24, 2023
Distribution
Nationwide

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FDA Recall TerminatedTerminated: April 5, 2024Historical recordClass II

Piperacillin and Tazobactam for Injection, USP, 4.5 grams per vial, Rx only, Mfg. for: Piramal Critical Care, Bethlehem, PA 18017, NDC 66794-218-41

by Astral SteriTech Private Ltd.

Reason
Lack of Assurance of Sterility
Published
May 24, 2023
Distribution
Nationwide

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FDA Recall TerminatedTerminated: April 5, 2024Historical recordClass II

Piperacillin and Tazobactam for Injection, USP 3.375 grams per vial, Rx only, Mfd for Meitheal Pharmaceuticals Chicago, IL 60631, NDC 71288-003-31

by Astral SteriTech Private Ltd.

Reason
Lack of Assurance of Sterility
Published
May 24, 2023
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: April 5, 2024Historical recordClass II

Piperacillin and Tazobactam for Injection, USP, 2.25 grams per vial, Rx only, Mfd for Meitheal Pharmaceuticals Chicago, IL 60631, NDC 71288-002-31

by Astral SteriTech Private Ltd.

Reason
Lack of Assurance of Sterility
Published
May 24, 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.

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