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Recall totals

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

37,142

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,799

Class I recallsReasonable probability of serious health consequences

24,349

Class II recallsTemporary or medically reversible health consequences

2,891

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 2,072 recalls

Newest recallhttps://www.fsis.usda.gov/recalls-alerts/fontanini-foods-llc-recalls-raw-frozen-pork-sausage-products-due-possible-foreignPublished September 25, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 28, 2026 ET

Summary (Year to date)

1,527 recalls have been announced year to date.
Aug 2026 was 24% lower than the previous complete period (Jul 2026: 240).
The highest complete period was Jun 2026 (297).
Sep 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,349
Class I	9,799
Class III	2,891
Not Yet Classified	1

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Recalls by class
Class	Recalls
Class II	24,349
Class I	9,799
Class III	2,891
Not Yet Classified	1

FDA Recall Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical recordClass II

Levetiracetam Oral Solution, USP, 100 mg/mL, packaged in a 16 fl oz (473 mL) bottle, Rx only, Manufactured for: Camber Pharmaceuticals, Inc., Piscataway, NJ 08854, By: Hetero, Hetero Labs Limited, Jeedimetla,Hyderabad - 500 055, India, NDC 31722-574-47

by Hetero Labs, Ltd. - Unit III

Reason: Presence of foreign substance (screw)
Published: December 6, 2017
Distribution: NJ

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FDA Recall Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical recordClass I

Yorgo Food's Inc.

Product: Party Tray: Yorgo's Foods PARTY TRAY ORIGINAL HOMMUS NET WT.…
Reason: Product may be contaminated with Listeria monocytogenes.
Published: December 6, 2017
Distribution: NY and NJ

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FDA Recall United States Terminated Historical recordClass I

Yorgo Food's Inc.

Product: Yorgo's Foods SUNDRIED TOMATO and BASIL HOMMUS NET WT 8 OZ (…
Reason: Product may be contaminated with Listeria monocytogenes.
Published: December 6, 2017
Distribution: NY and NJ

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FDA Recall United States Terminated Historical recordClass I

Yorgo Food's Inc.

Product: Yorgo's Foods TZATZIKI NET WT 8 OZ (227g) UPC: 7 56248 10053…
Reason: Product may be contaminated with Listeria monocytogenes.
Published: December 6, 2017
Distribution: NY and NJ

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FDA Recall United States Terminated Historical recordClass I

Yorgo Food's Inc.

Product: Yorgo's VEGAN HOPPIN SALAD NET WT. 12 OZ (340g) UPC: 7 56248…
Reason: Product may be contaminated with Listeria monocytogenes.
Published: December 6, 2017
Distribution: NY and NJ

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Data last updated: September 28, 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.