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Recall totals

All FDA and USDA recalls in Public Health Trace, June 2012 to November 2026.

37,449
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,872
Class I recallsReasonable probability of serious health consequences
24,509
Class II recallsTemporary or medically reversible health consequences
2,932
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 2,096 recalls
Most affected stateHawaii 200 recalls mention this state

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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)

  • 1,956 recalls have been announced year to date.
  • Oct 2026 was 4% higher than the previous complete period (Sep 2026: 209).
  • The highest complete period was Jun 2026 (300).
  • Nov 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 II24,509
Class I9,872
Class III2,932
Not Yet Classified2
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Recalls by class
ClassRecalls
Class II24,509
Class I9,872
Class III2,932
Not Yet Classified2

Showing 9,641–9,660 of 21,307 recalls

FDA Recall United States TerminatedTerminated: February 27, 2020Historical recordClass II

Wegmans Food Markets, Inc.

Product
Signature Crab Cake, Signature Crab Cake (2 pk), and Signatu…
Reason
Products contain undeclared soy.
Published
January 22, 2020
Distribution
Multiple states

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FDA Recall United States TerminatedTerminated: March 26, 2020Historical recordClass III

Bob's Red Mill Natural Foods, Inc.

Product
Garbanzo Beans or Chickpeas, sold under brand Bob's Red Mill…
Reason
Product is recalled due to the potential presence of glyphosate.
Published
January 22, 2020
Distribution
Garbanzo Beans were distributed in CA, C…

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FDA Recall United States TerminatedTerminated: March 26, 2020Historical recordClass III

Bob's Red Mill Natural Foods, Inc.

Product
13 Bean Soup Mix is sold under Bob's Red Mill brand, packag…
Reason
Product is recalled due to the potential presence of glyphosate.
Published
January 22, 2020
Distribution
Garbanzo Beans were distributed in CA, C…

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FDA Recall United States TerminatedTerminated: March 25, 2020Historical recordClass I

Fresh Unlimited Inc

Product
Chef Salad Kit: 8lbs packaged in cardboard box
Reason
Eggs used in the manufacture of the products may be contaminated with Listeria monocytogenes
Published
January 22, 2020
Distribution
Salad kits were sent to Logistics/Distri…

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FDA Recall United States TerminatedTerminated: March 25, 2020Historical recordClass I

Fresh Unlimited Inc

Product
Cobb Salad Kit: 8lbs packaged in cardboard box
Reason
Eggs used in the manufacture of the products may be contaminated with Listeria monocytogenes
Published
January 22, 2020
Distribution
Salad kits were sent to Logistics/Distri…

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FDA Recall United States TerminatedTerminated: March 25, 2020Historical recordClass I

Fresh Unlimited Inc

Product
Garden Salad Kit: 7lbs packaged in cardboard box
Reason
Eggs used in the manufacture of the products may be contaminated with Listeria monocytogenes
Published
January 22, 2020
Distribution
Salad kits were sent to Logistics/Distri…

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FDA Recall United States TerminatedTerminated: October 8, 2020Historical recordClass I

Gourmet International Ltd.

Product
Butler's Dark Chocolate with Irish Whisky, 3.52oz bar, UPC 8…
Reason
undeclared milk
Published
January 22, 2020
Distribution
CA CT IL IN MD…

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FDA Recall United States TerminatedTerminated: April 13, 2020Historical recordClass I

Veggie Noodle Co

Product
Cece's Veggie Co. brand Fresh Veggie Ramen with Chicken Brot…
Reason
Potential to be contaminated with Listeria monocytogenes
Published
January 22, 2020
Distribution
Multiple states

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FDA Recall TerminatedTerminated: September 28, 2022Historical recordClass III

SURE 48hr Confidence Unscented Original Solid Anti-Perspirant & Deodorant Net Wt 2.7 oz (76g) NDC# 41595-5513-2 UPC 8 83484 71794 3 Made in Canada and Distributed by Idelle Labs, Ltd., El Paso, TX 79912

by Idelle Labs

Reason
Labeling Product Contains Undeclared API: Active Ingredient on label is not the active ingredient in the product.
Published
January 15, 2020
Distribution
Nationwide

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FDA Recall TerminatedTerminated: September 28, 2022Historical recordClass III

SURE 48hr Confidence Regular Original Solid Anti-Perspirant & Deodorant Net Wt 2.7 oz (76g) NDC# 41595-5514-1 UPC 8 83484 717936 6 Made in Canada and Distributed by Idelle Labs, Ltd., El Paso, TX 79912

by Idelle Labs

Reason
Labeling Product Contains Undeclared API: Active Ingredient on label is not the active ingredient in the product.
Published
January 15, 2020
Distribution
Nationwide

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FDA Recall TerminatedTerminated: September 28, 2022Historical recordClass III

SURE 48hr Confidence Nourishing Coconut invisible solid Antiperspirant & Deodorant Net Wt 2.6 oz (73g) NDC# 41595-5547-1 UPC 8 83484 31020 5 Made in Canada and Distributed by Idelle Labs, Ltd., El Paso, TX 79912

by Idelle Labs

Reason
Labeling Product Contains Undeclared API: Active Ingredient on label is not the active ingredient in the product.
Published
January 15, 2020
Distribution
Nationwide

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FDA Recall TerminatedTerminated: September 28, 2022Historical recordClass III

SURE 48 hr Confidence Unscented invisible solid Anti-Perspirant & Deodorant, Net Wt. 2.6 oz (73g) NDC# 41595-5509-2 UPC 8 83484 71717 2 Made in Canada and Distributed by Idelle Labs, Ltd., El Paso, TX 79912

by Idelle Labs

Reason
Labeling Product Contains Undeclared API: Active Ingredient on label is not the active ingredient in the product.
Published
January 15, 2020
Distribution
Nationwide

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FDA Recall TerminatedTerminated: October 22, 2020Historical recordClass II

Blisovi Fe 1.5/30 (norethindrone acetate and ethinyl estradiol tablets USP and ferrous fumarate tablets 75mg), Rx Only, Distributed by: Lupin Pharmaceuticals Inc Baltimore, MD 21202, Manufactured for: Lupin Limited Pithampur 454775 INDIA 240875, NDC 68180-866-11

by Lupin Pharmaceuticals Inc.

Reason
Failed Tablet/Capsule Specifications: Complaints related to crumbling of tablets when popped out of the blister pack.
Published
January 15, 2020
Distribution
Nationwide

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FDA Recall United States OngoingHistorical recordClass II

TFI Holding dba Grey Ghost Bakery

Product
GREY GHOST BAKERY scratch-made cookies LEMON SUGAR NET WT 1.…
Reason
The product contains undeclared sulfites.
Published
January 15, 2020
Distribution
Product was shipped to the following sta…

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FDA Recall United States TerminatedTerminated: February 4, 2020Historical recordClass I

Reichel Foods Inc.

Product
Pro2Snax To The Max snack tray containing Sweet Gala Apples,…
Reason
Products are being recalled due to Listeria monocytogenes contamination.
Published
January 15, 2020
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: February 4, 2020Historical recordClass I

Reichel Foods Inc.

Product
Pro2Snax To The Max snack tray containing Sliced Apples, Har…
Reason
Products are being recalled due to Listeria monocytogenes contamination.
Published
January 15, 2020
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: May 21, 2020Historical recordClass II

Wayfare Health Foods LLC

Product
Plant Based WayFare Butterscotch Pudding Organic Dairy Free,…
Reason
Product is recalled due to consumer complaints for bloating of package, off flavors (sourness, tart), and textural issues (grittiness, lumpiness).
Published
January 15, 2020
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: May 21, 2020Historical recordClass II

Wayfare Health Foods LLC

Product
Plant Based WayFare Vanilla Pudding Organic Dairy Free, Item…
Reason
Product recalled due to consumer complaints for bloating of package, off flavors (sourness, tart), and textural issues (grittiness, lumpiness).
Published
January 15, 2020
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: May 21, 2020Historical recordClass II

Wayfare Health Foods LLC

Product
Plant Based WayFare Chocolate Pudding Organic Dairy Free, It…
Reason
Product recalled due to consumer complaints for bloating of package, off flavors (sourness, tart), and textural issues (grittiness, lumpiness).
Published
January 15, 2020
Distribution
Nationwide

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FDA Recall TerminatedTerminated: August 9, 2022Historical recordClass II

MYORISAN (isotretinoin capsules, USP), 20mg, packaged in 30-count Capsules (3 x 10 Prescription Packs) per box, Rx only, Distributed by: VersaPharm Inc. - An Akorn Company, Lake Forset, IL 60045; NDC 61748-302-13.

by Akorn, Inc.

Reason
Unit Dose Mispackaging: Customer complaint that a carton labeled as Myorisan 20 mg Capsules, USP erroneously contained one 10-count blister card of the 40 mg product in addition to two 10-count blister cards of the 20 mg product.
Published
January 8, 2020
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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