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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
Download CSV
Recalls by class
ClassRecalls
Class II24,509
Class I9,872
Class III2,932
Not Yet Classified2

Showing 8,621–8,640 of 21,307 recalls

FDA Recall United States TerminatedTerminated: November 24, 2020Historical recordClass II

EAGLE FAMILY FOODS GROUP LLC

Product
Nature's Promise Organic Lightly Salted Popcorn, 6 oz. bag,…
Reason
Foreign material, pieces of glass may be in the product
Published
October 7, 2020
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: November 24, 2020Historical recordClass II

EAGLE FAMILY FOODS GROUP LLC

Product
Cretors Organic Extra Virgin Olive Oil Popcorn, 4.4 oz. bag,…
Reason
Foreign material, pieces of glass may be in the product
Published
October 7, 2020
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: November 24, 2020Historical recordClass II

EAGLE FAMILY FOODS GROUP LLC

Product
365 Everyday Value Organic Classic Salted Popcorn, 6 oz. bag…
Reason
Foreign material, pieces of glass may be in the product
Published
October 7, 2020
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: November 24, 2020Historical recordClass II

EAGLE FAMILY FOODS GROUP LLC

Product
365 Whole Foods Market Organic Reduced fat &Sodium Popcorn,…
Reason
Foreign material, pieces of glass may be in the product
Published
October 7, 2020
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: November 24, 2020Historical recordClass II

EAGLE FAMILY FOODS GROUP LLC

Product
365 Whole Foods Market Organic White Cheddar Popcorn, 4 oz.…
Reason
Foreign material, pieces of glass may be in the product
Published
October 7, 2020
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: November 17, 2020Historical recordClass II

Hale And Hearty Soups, LLC

Product
WILD MUSHROOM BARLEY soup; Manufactured By: Hale & Hearty So…
Reason
Product may contain pieces of maggots.
Published
October 7, 2020
Distribution
Multiple states

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FDA Recall TerminatedTerminated: February 8, 2022Historical recordClass I

Red-E Tablet, Proprietary Blend 3000 mg**, packaged in 1-count plastic bag stapled with cardboard labeling.

by The Protein Shoppe

Reason
Marketed Without An Approved NDA/ANDA: product found to be tainted with sildenafil, an FDA approved drug for the treatment of male erectile dysfunction, making this an unapproved drug fro which the safety and efficacy have not been established and therefore subject to recall.
Published
September 30, 2020
Distribution
Nationwide

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FDA Recall TerminatedTerminated: May 22, 2023Historical recordClass II

Albuterol Sulfate Inhalation Aerosol, 90 mcg per actuation, 200 metered inhalations, Manufactured by: Catalent Pharma Solutions, 160 N Pharma Drive, Morrisville, NC 27560, Distributed by: Perrigo, Allegan, MI 49010 NDC 45802-088-01

by Perrigo Company PLC

Reason
Defective Delivery System: Sustained trend of failure to dispense complaints.
Published
September 30, 2020
Distribution
Nationwide

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FDA Recall TerminatedTerminated: May 19, 2022Historical recordClass I

Leafree Instant Hand Sanitizer Aloe Vera (ethyl alcohol 70% v/v), Kills 99.99% Germs, EDIBLE ALCOHOL, a) 100 mL bottles, UPC code 6970495860325, b) 300 mL bottles, UPC code 6970495860318, and c) 500 mL bottles, UPC code 6970495860301, Exclusively Distributed by: Corgiomed LLC, McLean, VA 22102, USA, Made in China.

by CORGIOMED LLC

Reason
Marketed without an Approved NDA/ANDA; product labeled as Edible Alcohol rendering the product an unapproved new drug and misbranded.
Published
September 30, 2020
Distribution
NC and MD

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FDA Recall United States TerminatedTerminated: December 8, 2020Historical recordClass II

Gilster-Mary Lee Corp.

Product
Cadia Organic Unsalted Microwave Popcorn, Net Wt. 8.4 oz (2…
Reason
Popcorn ingredient was recalled due to foreign matter: tempered glass between 3 mm and 7 mm in size
Published
September 30, 2020
Distribution
Distributed to grocery stores in the fol…

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FDA Recall United States TerminatedTerminated: December 8, 2020Historical recordClass II

Gilster-Mary Lee Corp.

Product
Microwave popcorn packaged in the following ways: 1) Full…
Reason
Popcorn ingredient was recalled due to foreign matter: tempered glass between 3 mm and 7 mm in size
Published
September 30, 2020
Distribution
Distributed to grocery stores in the fol…

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FDA Recall United States TerminatedTerminated: December 8, 2020Historical recordClass II

Gilster-Mary Lee Corp.

Product
Buttered microwave popcorn packaged in the following ways:…
Reason
Popcorn ingredient was recalled due to foreign matter: tempered glass between 3 mm and 7 mm in size
Published
September 30, 2020
Distribution
Distributed to grocery stores in the fol…

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FDA Recall United States TerminatedTerminated: December 8, 2020Historical recordClass II

Gilster-Mary Lee Corp.

Product
Light microwave popcorn packaged in the following ways: 1…
Reason
Popcorn ingredient was recalled due to foreign matter: tempered glass between 3 mm and 7 mm in size
Published
September 30, 2020
Distribution
Distributed to grocery stores in the fol…

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FDA Recall United States TerminatedTerminated: December 8, 2020Historical recordClass II

Gilster-Mary Lee Corp.

Product
Lightly salted microwave popcorn packaged in the following w…
Reason
Popcorn ingredient was recalled due to foreign matter: tempered glass between 3 mm and 7 mm in size
Published
September 30, 2020
Distribution
Distributed to grocery stores in the fol…

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FDA Recall United States OngoingHistorical recordClass III

Freshouse Produce

Product
Fresh from the Start Red B Potatoes, 3lb mesh bag, UPC 33383…
Reason
The firm received positive Environmental sampling results for Listeria monocytogenes.
Published
September 30, 2020
Distribution
Product was shipped to the following sta…

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FDA Recall United States OngoingHistorical recordClass II

Freshouse Produce

Product
Wegmans Valencia Oranges, 4lb mesh bag, UPC 77890 52363
Reason
The firm received positive Environmental sampling results for Listeria monocytogenes.
Published
September 30, 2020
Distribution
Product was shipped to the following sta…

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FDA Recall United States OngoingHistorical recordClass II

Freshouse Produce

Product
Freshouse Limes, 2lb mesh bag, UPC 33383 14683 & Nature Prom…
Reason
The firm received positive Environmental sampling results for Listeria monocytogenes.
Published
September 30, 2020
Distribution
Product was shipped to the following sta…

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FDA Recall United States OngoingHistorical recordClass II

Freshouse Produce

Product
Lemons, 2lb mesh bag sold under the brand names of Fresh fro…
Reason
The firm received positive Environmental sampling results for Listeria monocytogenes.
Published
September 30, 2020
Distribution
Product was shipped to the following sta…

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FDA Recall TerminatedTerminated: November 8, 2023Historical recordClass I

Nature Throid, 1.5 Grain (97.5 mg) Thyroid USP [Liothyronine (T3) 13.5 mcg, Levothyroxine (T4) 57 mcg], packaged in a) 30-count bottles (NDC 64727-3305-4), b) 60-count bottles (NDC 64727-3305-5), c) 90-count bottles (NDC 64727-3305-6), and 100-count bottles (NDC 64727-3305-1), Rx only, Manufactured by: RLC Labs Phoenix, AZ 85024, NDC 64727-3305-1

by RLC Labs Inc.

Reason
Subpotent Drug: FDA analysis found product to be subpotent
Published
September 23, 2020
Distribution
Nationwide

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FDA Recall TerminatedTerminated: November 8, 2023Historical recordClass I

Nature Throid, 2 Grain (130 mg) Thyroid USP [Liothyronine (T3) 18 mcg, Levothyroxine (T4) 76 mcg], packaged in a) 30-count bottles (NDC 64727-3308-4) and b)100-count bottles (NDC 64727-3308-1), Rx only, Manufactured by: RLC Labs Phoenix, AZ 85024

by RLC Labs Inc.

Reason
Subpotent Drug: FDA analysis found product to be subpotent
Published
September 23, 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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