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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

State: MD ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated November 9, 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

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

FDA Recall TerminatedTerminated: December 4, 2018Historical recordClass I

FIFTY SHADES 6000 capsule, Proprietary Raw Material 4550, 1-capsule packets, distributed by Express Pac Trading, UPC 4026666146056

by Gadget Island, Inc

Reason: Marketed without an Approved NDA/ANDA: undeclared Active Pharmaceutical Ingredients sildenafil, desmethyl carbodenafil and tadalafil.
Published: December 13, 2017
Distribution: Nationwide

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FDA Recall TerminatedTerminated: December 4, 2018Historical recordClass I

PapaZen 3300 capsule, Proprietary Blend 1800mg, 1-capsule packets, distributed by FX Power San Diego, CA 92108, UPC 718122032587

by Gadget Island, Inc

Reason: Marketed without an Approved NDA/ANDA: undeclared Active Pharmaceutical Ingredients sildenafil, desmethyl carbodenafil and tadalafil.
Published: December 13, 2017
Distribution: Nationwide

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FDA Recall TerminatedTerminated: December 4, 2018Historical recordClass I

RHINO 7 Platinum 5000, capsule, Proprietary Material: 750mg, 1-capsule packets, distributed by Fifty Shades Bayside, NY 11361, UPC 617135861224

by Gadget Island, Inc

Reason: Marketed without an Approved NDA/ANDA: undeclared Active Pharmaceutical Ingredients sildenafil, desmethyl carbodenafil and tadalafil.
Published: December 13, 2017
Distribution: Nationwide

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FDA Recall TerminatedTerminated: May 2, 2019Historical recordClass I

Pravastatin Sodium Tablets, USP, 40 mg, 30-count bottle, Rx only, Packaged for: International Laboratories, LLC. St. Petersburg, FL 33710, NDC 54458-925-16

by International Laboratories, Inc.

Reason: Labeling: Label mix-up, the product labeled as Pravastatin sodium tablets 40 mg was filled with Bupropion hydrochloride XL Tablets 300 mg.
Published: December 13, 2017
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: January 5, 2018Historical recordClass III

Clover Hill Dairy

Product: Clover Hill Dairy, Soft Ricotta
Reason: The firm had a deviation from the Standard of Procedure in the manufacture of Clover Hill Dairy, Soft Ricotta. The facility was temporarily storing whey in a raw milk silo, without cleaning and sanitizing the silo after raw milk use. The firm recalled the Clover Hill Dairy, Soft Ricotta.
Published: December 13, 2017
Distribution: One distributer located in Virginia as w…

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FDA Recall United States TerminatedTerminated: April 2, 2018Historical recordClass II

Plow And Hearth

Product: 89291 Cashew Tower (Plow and Hearth Chocolate Covered Cashew…
Reason: Plow and Hearth was notified by a manufacture of their product labeled as chocolate covered cashews were actually salted peanuts. The firm has decided to initiate a recall of the product. (Undeclared Allergen Issue).
Published: December 13, 2017
Distribution: The firms sells their product via online…

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FDA Recall United States TerminatedTerminated: February 12, 2018Historical recordClass II

JP's Delicacies LLC

Product: Holi Aioli, Lemon Basil 12oz bottle
Reason: JP s Delicacies LLC of Bloomfield NJ discovered during a walk thru of area stores, bulging bottles of Holi Aioli, Lemon Basil, 12oz Bottle, expiration date of 7/18/18. The firm has decided to initiated a recall because the products do not meet the firm s manufacturer standards.
Published: December 13, 2017
Distribution: Wegmans Stores NY, MA, NJ,VA,MD,PA

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FDA Recall United States TerminatedTerminated: May 31, 2018Historical recordClass I

Health Matters America Inc.

Product: Organic traditions brand DARK CHOCOLATE ALMONDS WITH CHILI,…
Reason: The imported products were found to contain undeclared milk (casein) based on analyses by the Canadian Food Inspection Agency (CFIA).
Published: December 13, 2017
Distribution: Retail stores located in Arizona, Califo…

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FDA Recall United States TerminatedTerminated: May 31, 2018Historical recordClass I

Health Matters America Inc.

Product: Organic traditions brand DARK CHOCOLATE ALMONDS, NET WT. 3.5…
Reason: The imported products were found to contain undeclared milk (casein) based on analyses by the Canadian Food Inspection Agency (CFIA).
Published: December 13, 2017
Distribution: Retail stores located in Arizona, Califo…

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FDA Recall United States TerminatedTerminated: May 31, 2018Historical recordClass I

Health Matters America Inc.

Product: Organic traditions brand DARK CHOCOLATE HAZELNUTS WITH CHILI…
Reason: The imported products were found to contain undeclared milk (casein) based on analyses by the Canadian Food Inspection Agency (CFIA).
Published: December 13, 2017
Distribution: Retail stores located in Arizona, Califo…

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FDA Recall United States TerminatedTerminated: May 31, 2018Historical recordClass I

Health Matters America Inc.

Product: Organic traditions brand DARK CHOCOLATE HAZELNUTS, NET WT.…
Reason: The imported products were found to contain undeclared milk (casein) based on analyses by the Canadian Food Inspection Agency (CFIA).
Published: December 13, 2017
Distribution: Retail stores located in Arizona, Califo…

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FDA Recall United States TerminatedTerminated: January 9, 2018Historical recordClass II

H. A. R. Maspeth Corp.

Product: WOLDONG WORLD'S BEST KIMCHI WHOLE CABBAGE KIMCHI PREMIUM 3LB…
Reason: Product contains undeclared sesame seeds.
Published: December 13, 2017
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: July 3, 2019Historical recordClass II

Leclerc Foods USA

Product: Fit & Active Chocolatey Chip Protein Meal Bars; UPC: 41498 1…
Reason: Firm received reports of flexible pieces of yellow plastic found in Fit & Active Chocolatey Chip Protein Meal Bars.
Published: December 13, 2017
Distribution: Connecticut, Delaware, Florida, Georgia,…

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FDA Recall TerminatedTerminated: September 1, 2020Historical recordClass II

Paroxetine Tablets USP, 30 mg, a) 30 count (NDC 68382-099-06), b) 500 count (NDC 68382-099-05), and c) 1000 count (NDC 68382-099-10) count bottles, Rx Only, Manufactured by: Cadila Healthcare Ltd, Ahmedabad, India Distributed by: Zydus Pharmaceuticals USA, Inc., Pennington, NJ 08534

by Zydus Pharmaceuticals USA Inc

Reason: Presence of Foreign Tablets/Capsules: Risperidone Tablets were found in bottle of Paroxetine Tablets
Published: December 6, 2017
Distribution: Nationwide

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FDA Recall TerminatedTerminated: August 9, 2019Historical recordClass II

Vertra Elemental Resistance (Octyl Methoxycinnamate 6%, Oxybenzone 5%, Titanium Dioxide 6.3%, Zinc Oxide 9.9%) Sun Protection Cream, SPF 50+, Net. Wt. 2.8 oz (80 g) tube in a carton, Distributed by Vertra/EAI-JR286, 20100 S Vermont Ave, Torrance, CA 90502, Made In Australia, UPC 8 94140 00103 0.

by EAI-JR286 INC

Reason: CGMP Deviations: products manufactured in a manner that may impact product quality that includes but is not limited to failed viscosity.
Published: December 6, 2017
Distribution: Nationwide

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FDA Recall TerminatedTerminated: May 11, 2020Historical recordClass II

Liothyronine Sodium Tablets, USP 25 mcg ,100-count bottles, Rx Only, Distributed by Perrigo Minneapolis, MN 55427, NDC 0574-0222-01

by Mayne Pharma Inc

Reason: Failed Dissolution Specifications.
Published: December 6, 2017
Distribution: Nationwide

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FDA Recall TerminatedTerminated: April 15, 2019Historical recordClass III

Duloxetine Delayed-Release Capsules USP, 30 mg, 30-count bottles, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202 United States, Manufactured by: Lupin Limited Goa 403 722 India, NDC 68180-295-06, UPC 368180295068

by Lupin Pharmaceuticals Inc.

Reason: Failed Dissolution Specification
Published: December 6, 2017
Distribution: Nationwide

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FDA Recall TerminatedTerminated: July 3, 2018Historical recordClass II

Clozapine Tablets USP, 100 mg, 500 count bottles, Rx only, Manufactured in Israel by: TEVA PHARMACEUTICALS IND, LTD, Jerusalem Israel, Manufactured For: TEVA PHARMACEUTICALS USA, North Wales, PA, NDC 00093-7772-05

by Teva Pharmaceuticals USA

Reason: Failed Tablet/Capsule Specifications; potential presence of broken tablets.
Published: December 6, 2017
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: July 23, 2021Historical recordClass II

Ahold Usa

Product: Ahold-Own Brands Whole Kernel Sweet Corn, 16 oz. Plastic Ba…
Reason: Ahold U.S.A., Inc. was notified by the Virginia Department of Agriculture that one of three retail samples of Whole Kernel Corn, 16 oz. tested positive for Listeria Monocytogenes on 11/13/2017. The firm has decided to initiate a recall of the product .
Published: December 6, 2017
Distribution: The firm distributed product to the foll…

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FDA Recall United States TerminatedTerminated: June 4, 2018Historical recordClass II

Reese Pharmaceutical Company

Product: Orange Flavor Immune Support Dietary Supplement Effervescent…
Reason: The label does not list "Sodium" in the ingredient statement.
Published: December 6, 2017
Distribution: Product was shipped to the following sta…

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Data last updated: November 9, 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.