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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
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 4,101–4,120 of 22,444 recalls

FDA Recall United States TerminatedTerminated: July 5, 2024Historical recordClass I

Freshy Foods, LLC

Product
Team Fresh & Go: Mixed Fruit Cup, packaged in 16oz plastic c…
Reason
potential contamination of Listeria monocytogenes
Published
August 30, 2023
Distribution
Facilities located in FL, LA, and MS

View recall →

FDA Recall United States TerminatedTerminated: July 5, 2024Historical recordClass I

Freshy Foods, LLC

Product
Team Fresh & Go: Cantaloupe Cup, packaged in 12oz plastic cu…
Reason
potential contamination of Listeria monocytogenes
Published
August 30, 2023
Distribution
Facilities located in FL, LA, and MS

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FDA Recall United States TerminatedTerminated: March 1, 2024Historical recordClass II

Inmar Supply Chain Solutions, LLC

Product
Multiple FDA-regulated products. Pallets
Reason
Potential exposure to rodents and rodent activity in the warehouse.
Published
August 30, 2023
Distribution
Nationwide

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FDA Recall OngoingHistorical recordClass III

Tobramycin Opthalmic Solution USP, 0.3%, 5mL bottle, Rx only, Manufactured for: Alembic Pharmaceuticals, Bedminster, NJ 07921, USA, NDC 62332-518-05

by ALEMBIC PHARMACEUTICALS, INC.

Reason
Failed Impurities/Degradation Specifications
Published
August 23, 2023
Distribution
Nationwide

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FDA Recall TerminatedTerminated: March 12, 2024Historical recordClass III

PLUVICTO 1,000MBq/mL (27 mCi/mL), lutetium Lu 177 vipivotide tetraxetan injection, 9.2 mL Single-dose vial, Manufacturer: Advanced Accelerator Appllications USA, Inc., 57 E. Willow Street NJ 07041, Milburn, USA, NDC 69488-010-61

by Advanced Accelerator Applications USA, Inc.

Reason
Labeling: Incorrect or Missing Lot and/or Exp Date: vials were labeled with the incorrect lot number and expiration date
Published
August 23, 2023
Distribution
Nationwide

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FDA Recall TerminatedTerminated: April 1, 2024Historical recordClass II

hello wild strawberry fluoride toothpaste, sodium fluoride 0.24% (0.15% w/v fluoride ion), NET WT 4.2 OZ (119 g), Distributed by Hello Products LLC, Montclair, NJ 07042, UPC 8 19156 02026 4 (carton), 12-count case GTIN: 20819156020268; strawberry tubes also sold in Strawberry 3-pack overwrap UPC 8 19156 02349 4, UPC 10819156023491 case; in the variety 3-pack of Strawberry + Unicorn + Grape UPC 8 19156 02332 6, UPC 10819156023323 case; and in a 24-count Toothpaste Floorstand, UPC 819156020684 (case).

by Colgate Palmolive Company

Reason
Labeling: Label Mix-Up: Some hello wild strawberry fluoride toothpaste, packaged in cartons labeled as hello wild strawberry fluoride toothpaste were incorrectly filled in tubes labeled as hello fresh watermelon fluoride free toothpaste.
Published
August 23, 2023
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: November 9, 2023Historical recordClass III

Lipari Foods Operating Company, LLC.

Product
IO Inspired Organics brand Organic Raw Walnut Halves & Piece…
Reason
undeclared walnuts in ingredient and contains statement
Published
August 23, 2023
Distribution
AL, FL, IL, IN, KY, MI, NY, OH, PA, WI,…

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FDA Recall United States TerminatedTerminated: December 21, 2023Historical recordClass I

Richin Trading Inc

Product
Tim Heung Yuen Black Melon Seed 6 oz., 12 oz. Ingredients:…
Reason
Undeclared allergens; soy and wheat
Published
August 23, 2023
Distribution
U.S. distribution to the following: CA,…

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FDA Recall United States TerminatedTerminated: September 17, 2024Historical recordClass III

Commercial Bakeries

Product
Simply MI-Delicious MI-DEL Swedish Style Ginger Snaps Net Wt…
Reason
Undeclared peanut
Published
August 23, 2023
Distribution
Distributed to distribution centers in I…

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FDA Recall United States TerminatedTerminated: September 17, 2024Historical recordClass III

Commercial Bakeries

Product
Trader Joe's Joe-Joe's Chocolate Vanilla Creme Flavored Wit…
Reason
Undeclared peanut
Published
August 23, 2023
Distribution
Distributed to distribution centers in I…

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FDA Recall United States TerminatedTerminated: September 17, 2024Historical recordClass III

Commercial Bakeries

Product
Trader Joe's Gluten Free Joe-Joe's Chocolate Vanilla Creme…
Reason
Undeclared peanut
Published
August 23, 2023
Distribution
Distributed to distribution centers in I…

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FDA Recall United States TerminatedTerminated: September 17, 2024Historical recordClass III

Commercial Bakeries

Product
Gluten Free MI-DEL Swedish Style Ginger Snaps Net Wt. 8 oz (…
Reason
Undeclared peanut
Published
August 23, 2023
Distribution
Distributed to distribution centers in I…

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FDA Recall United States TerminatedTerminated: September 17, 2024Historical recordClass III

Commercial Bakeries

Product
Benton's 100 Calorie Snack Packs Baked Chocolate Wafer Snack…
Reason
Undeclared peanut
Published
August 23, 2023
Distribution
Distributed to distribution centers in I…

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FDA Recall United States TerminatedTerminated: August 15, 2023Historical recordClass II

Get Fresh Produce, Inc.

Product
Garden Cut Romaine 1x1 Chopped 6/2 LB (product number 9386)…
Reason
Product may be contaminated with deer feces.
Published
August 23, 2023
Distribution
Illinois and Florida

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FDA Recall United States TerminatedTerminated: September 17, 2024Historical recordClass III

Commercial Bakeries

Product
Trader Joe's Tiniest Chocolate Chip Cookies Net Wt. 8 oz (22…
Reason
Undeclared peanut
Published
August 23, 2023
Distribution
Distributed to distribution centers in I…

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FDA Recall United States TerminatedTerminated: September 17, 2024Historical recordClass III

Commercial Bakeries

Product
Ruxton Chocolates Manning Brand Pumpkin Creme Cookies 19.5 o…
Reason
Undeclared peanut
Published
August 23, 2023
Distribution
Distributed to distribution centers in I…

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FDA Recall United States TerminatedTerminated: September 17, 2024Historical recordClass III

Commercial Bakeries

Product
Annie's Homegrown Gluten Free Bunny Grahams Cocoa & Vanilla…
Reason
Undeclared peanut
Published
August 23, 2023
Distribution
Distributed to distribution centers in I…

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FDA Recall United States TerminatedTerminated: August 15, 2023Historical recordClass II

Get Fresh Produce, Inc.

Product
Garden Cut Lettuce Greek Mix Salad (product number 10149) 10…
Reason
Product may be contaminated with deer feces.
Published
August 23, 2023
Distribution
Illinois and Florida

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FDA Recall United States TerminatedTerminated: January 10, 2024Historical recordClass II

Daily Meals Corp

Product
VEROCCA, Locally Handmade, ALFAJOR
Reason
Undeclared Allergen - Wheat, Milk, and Soybean Oil
Published
August 23, 2023
Distribution
Florida

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FDA Recall TerminatedTerminated: February 26, 2024Historical recordClass III

Dofetilide Capsules 500 mcg (0.5mg), 60-count bottle, Rx Only, Manufactured by Sun Pharmaceutical Industries Limited, Survey No. 259/15, Dadra-396 191, (U.T of D & NH), India, Distributed by: Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512. NDC 47335-063-86

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason
Out of Specification result observed in content uniformity testing
Published
August 16, 2023
Distribution
Nationwide

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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.

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