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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.

37,115
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
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/so-delicious-dairy-freer-issues-voluntary-recall-salted-caramel-cluster-non-dairy-frozen-dessertPublished September 15, 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 II24,343
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 7,721–7,740 of 17,327 recalls

FDA Recall United States Terminated Historical recordClass II

Bubbies Homemade Ice Cream and Desserts, Inc.

Product
Bubbies Mochi Ice Cream -lychee Item Code CS800001, UPC Code…
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

View recall →

FDA Recall United States Terminated Historical recordClass II

Bubbies Homemade Ice Cream and Desserts, Inc.

Product
Bubbies Mochi Ice Cream -Li Hing Mango Item Code CS800237, U…
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

View recall →

FDA Recall United States Terminated Historical recordClass II

Bubbies Homemade Ice Cream and Desserts, Inc.

Product
Bubbies Mochi Ice Cream -Green Tea Item Code CS800056, UPC C…
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

View recall →

FDA Recall United States Terminated Historical recordClass II

Bubbies Homemade Ice Cream and Desserts, Inc.

Product
Bubbies Mochi Ice Cream -Chocolate Vanilla Item Code CS81200…
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

View recall →

FDA Recall United States Terminated Historical recordClass II

Bubbies Homemade Ice Cream and Desserts, Inc.

Product
Bubbies Mochi Ice Cream -Chocolate Mint Item Code CS812083,…
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

View recall →

FDA Recall United States Terminated Historical recordClass II

Bubbies Homemade Ice Cream and Desserts, Inc.

Product
Bubbies Mochi Ice Cream -Chocolate Espresso Item Code CS8120…
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

View recall →

FDA Recall United States Terminated Historical recordClass II

Bubbies Homemade Ice Cream and Desserts, Inc.

Product
Bubbies Mochi Ice Cream -Chocolate Coconut Item Code CS81206…
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

View recall →

FDA Recall United States Terminated Historical recordClass II

Bubbies Homemade Ice Cream and Desserts, Inc.

Product
Bubbies Mochi Ice Cream -Blood Orange Item Code CS800490, UP…
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

View recall →

FDA Recall United States Terminated Historical recordClass II

Bubbies Homemade Ice Cream and Desserts, Inc.

Product
Bubbies Cookie Dough Ice Cream Bites -Sugar Cookie Item Code…
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

View recall →

FDA Recall United States Terminated Historical recordClass II

Bubbies Homemade Ice Cream and Desserts, Inc.

Product
Bubbies Cookie Dough Ice Cream Bites -Chocolate Chip 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

View recall →

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

View recall →

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 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

View recall →

FDA Recall Terminated Historical recordClass II

Ketamine 50 mg/5 mL in 0.9% Sodium Chloride Injection for IV or IM Use (concentration = 10 mg/mL), 6 mL Syringe, Rx Only, SCA Pharmaceuticals, Windsor, CT 06095, NDC 70004-0430-09.

by SCA Pharmaceuticals, LLC

Reason
Lack of Assurance of Sterility.
Published
August 28, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Clear Eyes Redness Relief Hand Pocket Pal Tray Display; each display (UPC 6 78112 25418 7) contains 48 each of Clear eyes REDNESS RELIEF (Glycerin 0.25%, Naphazoline hydrochloride 0.012%) eye drops, 0.2 FL OZ (6 mL) bottle, Handy Pocket Pal (UPC 6 78112 25418 7); Distributed by Medtech Products Inc., Tarrytown, NY 10591 A Prestige Brands Company.

by Medtech Products, Inc.

Reason
CGMP Deviations: concerns regarding the sufficiency of Quality Assurance controls over critical systems in the manufacturing facility that could impact the product quality of the finished products.
Published
August 28, 2019
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.