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Recall totals

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

37,066

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,786

Class I recallsReasonable probability of serious health consequences

24,313

Class II recallsTemporary or medically reversible health consequences

2,876

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 recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/whole-foods-market-issues-allergy-alert-undeclared-egg-cabricharme-cheesePublished September 11, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 12, 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	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

FDA Recall United States Terminated Historical recordClass II

Joseph Epstein Food Enterprises, Inc. dba MamaMancini's

Product: Mama Mancini s Stuffed Shells with Sauce and Mozzarella Chee…
Reason: Products have the potential to be contaminated with Listeria monocytogenes.
Published: December 18, 2024
Distribution: The recalled product was distributed to…

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FDA Recall United States Terminated Historical recordClass I

F&S Produce West LLC

Product: Mediterranean Inspired Party Tray; Sell by dates 11/27/2024-…
Reason: Mediterranean party tray contains tzatziki sauce made with potentially contaminated (Salmonella) cucumbers.
Published: December 18, 2024
Distribution: 187 retail locations in AZ, CA, ID, MT,…

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FDA Recall United States Terminated Historical recordClass II

House Of Flavors, Inc.

Product: Giant Eagle churned Butter Pecan Reduced Fat 48FLOZ, UPC 030…
Reason: Undeclared soy (soy lecithin).
Published: December 18, 2024
Distribution: Retail stores in MD, OH, PA, and WV

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FDA Recall United States Terminated Historical recordClass II

Piazza Produce (dba CIBUS Fresh)

Product: CIBUS Fresh, Jack & Olive, Sprig and Sprout branded Autumn T…
Reason: Spreadable brie, 2/3lb used in sandwich was recalled by manufacturer due to possible Listeria monocytogenes contamination
Published: December 18, 2024
Distribution: IL IN KY MO OH TN

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FDA Recall United States Ongoing Historical recordClass II

Tipp Distributors, Inc. dba Novamex

Product: Jarritos Coconut Water 17.5 fl oz cans- 12 cans per carton
Reason: The hermetic seal on the lid of the cans may be compromised
Published: December 18, 2024
Distribution: Only in the US. States: AL, AR, DE, FL,…

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FDA Recall United States Terminated Historical recordClass II

Deseret Biologicals Inc

Product: DesBio lunaSOMM Natural Sleep Support Dietary Supplement ca…
Reason: Product contains undeclared soy lecithin.
Published: December 18, 2024
Distribution: Nationwide

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FDA Recall United States Ongoing Historical recordClass II

NESTLE HEALTH SCIENCE

Product: Nestle Health Services Nutren 2.0 kCal/mL, Calorically Dense…
Reason: Labeling Error. Nutren 2.0 UltraPak pouches were mislabeled with an Isosource 1.5 label.
Published: December 18, 2024
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass II

SUGAR FOODS LLC

Product: Fresh Gourmet TORTILLA STRIPS SANTA FE SYTLE NET WT 3.5 OZ (…
Reason: Undeclared Wheat. The firm was notified by a consumer that they found crispy onions in the packaging of the tortilla strips. The onions contain wheat which is not listed on the packaging for the tortilla strips.
Published: December 18, 2024
Distribution: Product was shipped to the following sta…

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FDA Recall Terminated Historical recordClass II

Lisdexamfetamine Dimesylate Capsules, 10 mg, 100 Capsules per bottle, Rx only, Distributed by: Lannet Company, Philadelphia, PA 19136, NDC: 0527-4661-37

by Lannett Company Inc.

Reason: Failed Content Uniformity Specifications: Product failed to meet the action limits for stratified content uniformity.
Published: December 11, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Cinacalcet Tablets, 90 mg, 30-count bottle, Rx only, Manufactured for: AvKARE, Pulaski, TN 38478, NDC 42291-461-30

by AvKARE

Reason: CGMP deviations: Presence of Nitrosamine Drug Substance Related Impurity (NDSRI), N-Nitroso-Cinacalcet above acceptable intake limit.
Published: December 11, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Cinacalcet Tablets, 60 mg, 30-count bottle, Rx only, Manufactured for: AvKARE, Pulaski, TN 38478, NDC 42291-460-30

by AvKARE

Reason: CGMP deviations: Presence of Nitrosamine Drug Substance Related Impurity (NDSRI), N-Nitroso-Cinacalcet above acceptable intake limit.
Published: December 11, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Cinacalcet Tablets, 30 mg, 30-count bottle, Rx only, Manufactured for: AvKARE, Pulaski, TN 38478, NDC 42291-459-30

by AvKARE

Reason: CGMP deviations: Presence of Nitrosamine Drug Substance Related Impurity (NDSRI), N-Nitroso-Cinacalcet above acceptable intake limit.
Published: December 11, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Duloxetine DR Capsules USP 60 mg, a) 30 count (NDC 57237-019-30), b) 90 count NDC 57237-019-90 and c) 1000 count (NDC 57237-019-99) bottles, Distributed by: Rising Pharmaceuticals, Inc., East Brunswick, NJ

by Rising Pharma Holding, Inc.

Reason: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above recommended interim limit
Published: December 11, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Duloxetine Delayed-Release Capsules USP, 30 mg, a) 30 count (NDC 57237-018-30), b) 90 count (NDC 57237-018-90) and c) 1000 count (NDC 57237-018-99) bottles, Rx only, Distributed by: Rising Pharma Holdings, Inc., East Brunswick, NJ

by Rising Pharma Holding, Inc.

Reason: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above recommended interim limit
Published: December 11, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Duloxetine Delayed-Release Capsules USP, 20 mg, 60 count bottles, Rx only, Distributed by: Rising Pharma Holdings, Inc., East Brunswick, NJ NDC 57237-017-60

by Rising Pharma Holding, Inc.

Reason: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above recommended interim limit
Published: December 11, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Sunitinib Malate Capsules, 25 mg, 28-count bottles, Rx Only, Manufactured for: AvKARE, Pulaski, TN 38478. NDC 42291-902-28

by AvKARE

Reason: Labeling: Label Mix-Up
Published: December 11, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Sunitinib Malate Capsules, 12.5 mg, 28-count bottles, Rx Only, Manufactured for: AvKARE, Pulaski, TN 38478. NDC 42291-901-28

by AvKARE

Reason: Labeling: Label Mix-Up
Published: December 11, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass III

Esomeprazole Magnesium for Delayed-Release Oral Suspension 40 mg, 30 Single-Dose Packets, Rx Only, Manufactured by: Zydus Lifesciences Ltd. Ahmedabad, India, Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534, NDC 68382-849-94. Packaged in sachets

by Zydus Pharmaceuticals (USA) Inc

Reason: Labeling: Not Elsewhere Classified - Wrong NDC number
Published: December 11, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Diltiazem Hydrochloride Extended-Release Capsules, USP 120mg, Twice-a-Day Dosage, Rx Only, 100 Capsules per bottle, Mfd for: Northstar Rx LLC, Memphis, TN, Mfd by: Glenmark Pharmaceuticals Limited, Pithampur, Madhya Pradesh India, NDC 16714-555-01.

by Glenmark Pharmaceuticals Inc., USA

Reason: cGMP Deviations: Presence of N-nitroso-Desmethyl-Diltiazem impurity above FDA recommended interim limit.
Published: December 11, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Diltiazem Hydrochloride Extended-Release Capsules, USP 90mg, Twice-a-Day Dosage, Rx Only, 100 Capsules per bottle, Mfd for: Northstar Rx LLC, Memphis, TN, Mfd by: Glenmark Pharmaceuticals Limited, Pithampur, Madhya Pradesh India, NDC 16714-554-01.

by Glenmark Pharmaceuticals Inc., USA

Reason: cGMP Deviations: Presence of N-nitroso-Desmethyl-Diltiazem impurity above FDA recommended interim limit.
Published: December 11, 2024
Distribution: Nationwide

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Data last updated: September 12, 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.