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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

Newest recallhttps://www.fsis.usda.gov/recalls-alerts/fsis-issues-public-health-alert-meat-and-poultry-products-due-misbranding-andPublished November 6, 2026

Most affected stateHawaii 200 recalls mention this state

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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated November 8, 2026 ET

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

Recalls by class
Class	Recalls
Class II	24,509
Class I	9,872
Class III	2,932
Not Yet Classified	2

Recalls by class
Class	Recalls
Class II	24,509
Class I	9,872
Class III	2,932
Not Yet Classified	2

FDA Recall TerminatedTerminated: April 18, 2019Historical recordClass II

TravelEase, Homeopathic Oral Spray, 1.38 fl. oz (41ml), Manufactured for Sprayology Gaithersburg. MD 20879NDC 61096-0007-1. and Tester NDC 61096-1007-1

by Sprayology

Reason: CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.
Published: November 7, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: April 18, 2019Historical recordClass II

SleepEase, Homeopathic Oral Spray, 1.38 fl. oz (41ml), Manufactured for Sprayology Gaithersburg. MD 20879.NDC 61096-0001-1 and Tester NDC 6196-1001-1

by Sprayology

Reason: CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.
Published: November 7, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: April 18, 2019Historical recordClass II

DigestivEase, Homeopathic Oral Spray, 1.38 fl. oz (41ml), Manufactured for Sprayology Gaithersburg. MD 20879.NDC 61096-0005-1

by Sprayology

Reason: CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.
Published: November 7, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: April 18, 2019Historical recordClass II

Cold + Flu Relief, Homeopathic Oral Spray, 1.38 fl. oz (41ml), Manufactured for Sprayology Gaithersburg. MD 20879. NDC 61096-0002-1

by Sprayology

Reason: CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.
Published: November 7, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: April 18, 2019Historical recordClass II

AllergEase, Homeopathic Oral Spray, 1.38 fl. oz (41ml), Manufactured for Sprayology Gaithersburg. MD 20879. NDC 61096-0003-1

by Sprayology

Reason: CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.
Published: November 7, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: April 18, 2019Historical recordClass II

Bone Builder, Homeopathic Oral Spray, 1.38 fl. oz (41ml), Manufactured for Sprayology Gaithersburg. MD 20879. NDC 61096-0012-1 and Tester NDC 61096-1012-1

by Sprayology

Reason: CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.
Published: November 7, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: April 18, 2019Historical recordClass II

MenoPower, Homeopathic Oral Spray, 1.38 fl. oz (41ml), Manufactured for Sprayology Gaithersburg. MD 20879. NDC 61096-0014-1 and Tester NDC 61096-1014

by Sprayology

Reason: CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.
Published: November 7, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: April 18, 2019Historical recordClass II

Woman Power, Homeopathic Oral Spray, 1.38 fl. oz (41ml), Manufactured for Sprayology Gaithersburg. MD 20879 NDC 61096-0034-1 and Tester NDC 61096-1034-1

by Sprayology

Reason: CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.
Published: November 7, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: April 18, 2019Historical recordClass II

Brain Power,Homeopathic Oral Spray, 1.38 fl. oz (41ml), Manufactured for Sprayology Gaithersburg. MD 20879. NDC 61096-0033-1

by Sprayology

Reason: CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.
Published: November 7, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: April 18, 2019Historical recordClass II

Man Power, Homeopathic Oral Spray, 1.38 fl. oz (41ml), Manufactured for Sprayology Gaithersburg. MD 20879. NDC 61096-0025-1 and Tester NDC 61096-1025-1

by Sprayology

Reason: CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.
Published: November 7, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: April 18, 2019Historical recordClass II

Rejuvenation Plus, Homeopathic Oral Spray, 1.38 fl. oz (41ml), Manufactured for Sprayology Gaithersburg. MD 20879 NDC 61096-0035-1

by Sprayology

Reason: CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.
Published: November 7, 2018
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: February 25, 2019Historical recordClass II

Bakkavor Foods USA, Inc.

Product: Trader Joe's Tomato & Basil Hummus Dip, 7 oz. plastic contai…
Reason: Hummus was recalled due to potential Salmonella and/or Listeria monocytogenes contamination
Published: November 7, 2018
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: February 25, 2019Historical recordClass II

Bakkavor Foods USA, Inc.

Product: Trader Joe's Hummus quartet; 20 oz. plastic container; Spic…
Reason: Hummus was recalled due to potential Salmonella and/or Listeria monocytogenes contamination
Published: November 7, 2018
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: March 11, 2019Historical recordClass II

World Variety Produce Inc.

Product: Melissa's Hatch Chile Clean Snax, with Chia and flaxseed; 6.…
Reason: Firm discovered that Hatch Chile Clean Snax lists peanuts in the ingredient list but does not list peanuts under the allergen information.
Published: November 7, 2018
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: November 15, 2018Historical recordClass II

Wegmans Food Markets, Inc.

Product: Wegmans Hummus, NET WT 32 OZ (2 LB) 908g, UPC: 77890-26221 a…
Reason: Product contains foreign material (plastic).
Published: November 7, 2018
Distribution: Wegmans stores in NY, MA, NJ, PA, MD, VA…

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FDA Recall United States TerminatedTerminated: February 14, 2019Historical recordClass I

CFS West Holdings Inc

Product: Houlihan's Creamy Garlic Ranch Dressing potentially labeled…
Reason: A complaint received from a customer that a case of Creamy Ranch with Garlic was mislabeled as Horseradish Sauce. The ranch dressing contains the major food allergen of milk which is not declared on the label for the horseradish sauce.
Published: November 7, 2018
Distribution: Distributed to distributors in IL, MD, a…

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FDA Recall United States TerminatedTerminated: November 14, 2018Historical recordClass I

SLR FOOD Distribution, Inc.

Product: SUGAR MELON CANDY / WAX GOURD The product comes in a 7.04oz…
Reason: Product contains undeclared sulfites.
Published: November 7, 2018
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: January 30, 2019Historical recordClass II

Lone Star Bakery, Inc

Product: Veggie Pie packaged in a paper carton, Net Wt 6 OZ, Keep Fro…
Reason: Potential to contain a foreign object.
Published: November 7, 2018
Distribution: Texas, Indiana, Maryland, California and…

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FDA Recall United States TerminatedTerminated: January 30, 2019Historical recordClass II

Lone Star Bakery, Inc

Product: Spinach and Mushroom Pie, Net Wt. 6 OZ, packaged in a paper…
Reason: Potential to contain a foreign object.
Published: November 7, 2018
Distribution: Texas, Indiana, Maryland, California and…

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FDA Recall TerminatedTerminated: September 30, 2020Historical recordClass II

Bumetanide Tablets, USP, 2 mg, 100-count bottle, Rx only, Manufactured by: Upser-Smith Laboratories, LLC, Maple Grove, MN 55369, NDC 0832-0542-11

by Upsher Smith Laboratories, Inc.

Reason: Failed impurities/ degradation specifications: Product is Out of Specification for an unspecified degradation product.
Published: October 31, 2018
Distribution: Nationwide

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Data last updated: November 8, 2026 ET

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.