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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.

37,118
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,793
Class I recallsReasonable probability of serious health consequences
24,343
Class II recallsTemporary or medically reversible health consequences
2,887
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 II24,343
Class I9,793
Class III2,887
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,343
Class I9,793
Class III2,887
Not Yet Classified1

Showing 9,581–9,600 of 20,945 recalls

FDA Recall United States Terminated Historical recordClass II

Bubbies Homemade Ice Cream and Desserts, Inc.

Product
Bubbies Cookie Dough Ice Cream Bites - Brownie Batter, Item…
Reason
Bubbies Mochi Ice Cream, Bubbles Cookie Dough Ice Cream Bites,Trader Joe's Mochi six-piece products because of the potential for "free-floating" foreign plastic pieces in the product.
Published
September 18, 2019
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Hometown Food Company

Product
Martha White Gluten Free Sweet Yellow Cornbread & Muffin Mix…
Reason
Product tested positive for gluten but is labeled as Gluten free
Published
September 18, 2019
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Mountain Mel's Essential Goods LLC

Product
The Milk Lady's Herbal Tea, packaged loose leaf in aluminum…
Reason
Herbal Tea product is recalled due to a potential contamination with Salmonella.
Published
September 11, 2019
Distribution
CA, OR, and WA.

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FDA Recall United States Terminated Historical recordClass I

Mountain Mel's Essential Goods LLC

Product
Peaceful Baby For Colic & Teething Discomfort Herbal Tea, pa…
Reason
Herbal Tea product is recalled due to a potential contamination with Salmonella.
Published
September 11, 2019
Distribution
CA, OR, and WA.

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FDA Recall United States Terminated Historical recordClass I

Mountain Mel's Essential Goods LLC

Product
Diges-Teas Herbal Tea, packaged loose leaf in aluminum tin,…
Reason
Herbal Tea product is recalled due to a potential contamination with Salmonella.
Published
September 11, 2019
Distribution
CA, OR, and WA.

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FDA Recall Terminated Historical recordClass II

Vivitrol (naltrexone for extended-release injectable suspension) 380 mg/vial. Each Carton Contains: 1) One vial of 380 mg of Vivitrol, 2) One vial containing 4 mL of diluent, 3) One 5-mL prepackaged syringe, 4) One 20-gauge 1-inch needle, 5) Two 20-gauge 1.5-inch safety needles, 6) Two 20-gauge 2-inch safety needles. Rx Only. Manufactured and marketed by: Alkermes, Inc. Kit NDC: 65757-300-01

by Alkermes Inc

Reason
Labeling: Not Elsewhere Classified. Drug product kit recalled due to 1 inch needles being placed in the 1 1/2 inch needle cardboard sleeve labelled as administration needles. The product vial is not impacted.
Published
September 4, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

RELPAX (eletriptan HBr) tablets, 40 mg, packaged in a) 6-count (1 card x 6 tablets) per carton, NDC 0049-2340-45; b) 12-count (2 cards x 6 tablets) per carton, NDC 0049-2340-05, Rx only, Made in Ireland, Distributed by Pfizer Roerig, Division of Pfizer Inc., NY, NY 10017.

by Pfizer Inc.

Reason
Microbial Contamination of Non-Sterile Products: contamination with Burkholderia and Pseudomonas.
Published
September 4, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Simvastatin Tablets, USP 40 mg. Rx Only 1000 Count Bottles Manufactured by: Aurolife Pharma LLC Dayton NJ 08810 Manufactured for: Aurobindo Pharma USA, Inc. Dayton, NJ 08810 NDC 65862-053-99

by Aurobindo Pharma USA Inc.

Reason
Labeling; Incorrect or Missing Lot and/or Exp Date; some bottles labeled with lot number 05318054B instead of 05318034B
Published
September 4, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Eptifibatide Injection, a) 20 mg/10 mL (2 mg/mL),10 mL Single Use Vial, NDC 17478-902-10, b) 200 mg/100 mL (2 mg/mL), 100 mL Single-use Vial, NDC 17478-902-90, For Intravenous Use Only, Rx Only, Manufactured by: Akorn Inc., Lake Forest, IL 60045.

by Akorn, Inc.

Reason
Failed Impurities/Degradation Specifications: Out of Specification (OOS) for known impurity, D-aspartic acid.
Published
September 4, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Eptifibatide Injection, 75 mg/100 mL (0.75 mg/mL), 100 mL Single-use Vial, For Intravenous Use Only, Rx Only, Manufactured by: Akorn Inc., Lake Forest, IL 60045, NDC 17478-903-90.

by Akorn, Inc.

Reason
Short Fill: fill volume was out of specification at 94 mL (specification: no less than 100 mL) and Failed Impurities/Degradation Specifications: Out of Specification (OOS) for known impurity, D-aspartic acid.
Published
September 4, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Eptifibatide Injection, 75 mg/100 mL (0.75 mg/mL), 100 mL Single-use Vial, For Intravenous Use Only, Rx Only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045, NDC 17478-903-90.

by Akorn, Inc.

Reason
Failed Impurities/Degradation Specifications: Out of Specification (OOS) for known impurity, D-aspartic acid.
Published
September 4, 2019
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Olive Bakery

Product
Red/ Walnut bread packages contain two bread pastries filled…
Reason
Product sold 8/6/19 & 8/11/19 - Label declares flour but not wheat; and walnuts are visible through the clear package but label does not declare walnut. Product sold 8/12/19 - Label declares flour but not wheat.
Published
September 4, 2019
Distribution
distributed in OR and WA

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FDA Recall United States Terminated Historical recordClass II

Olive Bakery

Product
Sweet Potato bread packages contain two bread pastries fille…
Reason
Label declares flour but does not declare wheat.
Published
September 4, 2019
Distribution
distributed in OR and WA

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FDA Recall United States Terminated Historical recordClass II

Olive Bakery

Product
Chestnut bread packages contain two bread pastries filled wi…
Reason
Label declares flour but does not declare wheat.
Published
September 4, 2019
Distribution
distributed in OR and WA

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FDA Recall United States Terminated Historical recordClass II

Olive Bakery

Product
Peanut Butter bread packages contain two bread pastries fill…
Reason
Label declares flour but does not declare wheat. Product contains Non-Dairy Cream but label does not declare this sub-ingredient Soy Lecithin.
Published
September 4, 2019
Distribution
distributed in OR and WA

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FDA Recall United States Terminated Historical recordClass II

Olive Bakery

Product
Cream Horns packages contain one bread pastry filled with no…
Reason
Label declares flour but does not declare wheat. Label declares Non-Dairy Whipped Cream but does not declare its sub-ingredients Soy Lecithin.
Published
September 4, 2019
Distribution
distributed in OR and WA

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FDA Recall United States Terminated Historical recordClass II

Olive Bakery

Product
Bavarian bread packages contain two bread pastries filled wi…
Reason
Label declares flour but does not declare wheat. Product contains Non-Dairy Cream but label does not declare this sub-ingredient Soy Lecithin.
Published
September 4, 2019
Distribution
distributed in OR and WA

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FDA Recall United States Terminated Historical recordClass II

Olive Bakery

Product
Mocha Cream bread packages contain two bread pastries and ea…
Reason
Label declares flour but does not declare wheat. Almond is visible through a clear package but label does not declare almond. Product also contains Non-Dairy Cream but label does not declare this sub-ingredient Soy Lecithin.
Published
September 4, 2019
Distribution
distributed in OR and WA

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FDA Recall United States Terminated Historical recordClass II

Olive Bakery

Product
Cream bread packages contain two bread pastries filled with…
Reason
Label declares flour but does not declare wheat. Product contains Non-Dairy Cream but label does not declare this sub-ingredient Soy Lecithin.
Published
September 4, 2019
Distribution
distributed in OR and WA

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FDA Recall United States Terminated Historical recordClass II

Olive Bakery

Product
Peanut Crunch bread packages contain two bread pastries with…
Reason
Label declares flour but does not declare wheat.
Published
September 4, 2019
Distribution
distributed in OR and WA

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.