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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
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/whole-foods-market-issues-allergy-alert-undeclared-egg-cabricharme-cheesePublished September 11, 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 II24,313
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 3,321–3,340 of 17,993 recalls

FDA Recall Terminated Historical recordClass II

Cardioplegia Solution, Induction 8:1 High Potassium, 108 mEq K, packaged in 500 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0102-1.

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

View recall →

FDA Recall Terminated Historical recordClass II

Cardioplegia Solution, Induction 4:1, HIGH POTASSIUM/low tromethamine, 36 mEq K, packaged in 500 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-0101-1.

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

View recall →

FDA Recall Terminated Historical recordClass II

Cardioplegia Solution, Induction 4:1, High Potassium, 60 mEq K, packaged in 830 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0100-1.

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

View recall →

FDA Recall Terminated Historical recordClass II

Transplant Solution (Plasma-Lyte A), packaged in 165 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0014-2.

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

View recall →

FDA Recall Terminated Historical recordClass II

Microplegia Solution, MSA/MSG 0.92 Molar with CP2D, packaged in 120 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0012-2.

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

View recall →

FDA Recall Terminated Historical recordClass II

Cardioplegia Solution, Warm Induction 4:1 HIGH POTASSIUM/low tromethamine, 40 mEq K, packaged in 500 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0011-1.

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

View recall →

FDA Recall Terminated Historical recordClass II

Cardioplegia Solution, Reperfusate 4:1 low potassium/low tromethamine, 15 mEq K, packaged in 500 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0009-1.

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

View recall →

FDA Recall Terminated Historical recordClass II

Cardioplegia Solution, Reperfusate 4:1 low potassium, 15 mEq K, packaged in 477.5 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0008-1.

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

View recall →

FDA Recall Terminated Historical recordClass II

Cardioplegia Solution, Reperfusate 4:1 low potassium, 7.5 mEq K, packaged in 238.75 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0007-1.

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

View recall →

FDA Recall Terminated Historical recordClass II

Cardioplegia Solution, Reperfusate No Potassium, packaged in 477.5 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0006-1.

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

View recall →

FDA Recall Terminated Historical recordClass II

Cardioplegia Solution, Reperfusate No Potassium, packaged in 238.75 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0005-1.

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

View recall →

FDA Recall Terminated Historical recordClass II

Cardioplegia Solution, Warm Induction 4:1 High Potassium (40 mEq) packaged in 500 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0002-1.

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

View recall →

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

View recall →

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…

View recall →

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…

View recall →

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…

View recall →

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…

View recall →

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…

View recall →

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…

View recall →

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…

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.