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Recall totals

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

37,271

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,852

Class I recallsReasonable probability of serious health consequences

24,397

Class II recallsTemporary or medically reversible health consequences

2,897

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 2,085 recalls

Newest recallhttps://www.fsis.usda.gov/recalls-alerts/kayem-foods-inc--recalls-meat-and-poultry-products-due-possible-temperature-abusePublished October 17, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated October 19, 2026 ET

Summary (Year to date)

1,739 recalls have been announced year to date.
Sep 2026 was 15% higher than the previous complete period (Aug 2026: 182).
The highest complete period was Jun 2026 (300).
Oct 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,397
Class I	9,852
Class III	2,897
Not Yet Classified	2

Recalls by class
Class	Recalls
Class II	24,397
Class I	9,852
Class III	2,897
Not Yet Classified	2

FDA Recall CompletedHistorical recordClass II

BD ChloraPrep Clear, 2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (IPA) Sterile Solution, 0.03mL (1 ml) each, 60 applicators in carton, applicator is sterile if package is intact. CareFusion 213, LLC, El Paso, TX 79912, subsidiary of Becton, Dickinson and Co., NDC 54365-400-31 REF 930480 Product is packaged in the following manner: There is one (1) sterile applicator (sponge) per pouch. Each inner carton contains sixty (60) pouches. There are four (4) inner cartons per shipping case (total of 240 pouches per case).

by CareFusion 213, LLC

Reason: Stability data does not support expiry: Shelf-life of the impacted lots of BD ChloraPrep" Clear 1 mL Applicator cannot be substantiated beyond 12-months although labeled with 36-month expiry. Stability studies indicate that the impacted lots, if stored at 30¿C/75% relative humidity continuously beyond 12 months, may exhibit growth of Aspergillus penicillioides.
Published: September 27, 2023
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: January 10, 2025Historical recordClass III

Great Lakes Cheese, Inc.

Product: HEB Easy Melt Salsa Queso, with Tomatoes, Jalapeno Peppers &…
Reason: Refrigerated pasteurized process cheese products may not be refrigerated at customer level due to labeled refrigeration requirements varying on finished product labels.
Published: September 27, 2023
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: January 10, 2025Historical recordClass III

Great Lakes Cheese, Inc.

Product: Pasteurized Prepared Cheese Product, Queso Blanco, Half the…
Reason: Refrigerated pasteurized process cheese products may not be refrigerated at customer level due to labeled refrigeration requirements varying on finished product labels.
Published: September 27, 2023
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: January 10, 2025Historical recordClass III

Great Lakes Cheese, Inc.

Product: Hill Country Fare Melt'n Cheese, Pasteurized Prepared Cheese…
Reason: Refrigerated pasteurized process cheese products may not be refrigerated at customer level due to labeled refrigeration requirements varying on finished product labels.
Published: September 27, 2023
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: January 10, 2025Historical recordClass III

Great Lakes Cheese, Inc.

Product: Pasteurized Process Cheese Spread packaged under the followi…
Reason: Refrigerated pasteurized process cheese products may not be refrigerated at customer level due to labeled refrigeration requirements varying on finished product labels.
Published: September 27, 2023
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: January 10, 2025Historical recordClass III

Great Lakes Cheese, Inc.

Product: Harris Tetter Cheesy Melt, Pasteurized Prepared Cheese Produ…
Reason: Refrigerated pasteurized process cheese products may not be refrigerated at customer level due to labeled refrigeration requirements varying on finished product labels.
Published: September 27, 2023
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: January 10, 2025Historical recordClass III

Great Lakes Cheese, Inc.

Product: Pasteurized Prepared Cheese Product packaged under the follo…
Reason: Refrigerated pasteurized process cheese products may not be refrigerated at customer level due to labeled refrigeration requirements varying on finished product labels.
Published: September 27, 2023
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: January 10, 2025Historical recordClass III

Great Lakes Cheese, Inc.

Product: Great Value Melt'n Dip Easy Melt Cheese, Reduced Fat Pasteur…
Reason: Refrigerated pasteurized process cheese products may not be refrigerated at customer level due to labeled refrigeration requirements varying on finished product labels.
Published: September 27, 2023
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: January 10, 2025Historical recordClass III

Great Lakes Cheese, Inc.

Product: Pasteurized Prepared Cheese Product, packaged under the foll…
Reason: Refrigerated pasteurized process cheese products may not be refrigerated at customer level due to labeled refrigeration requirements varying on finished product labels.
Published: September 27, 2023
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: January 10, 2025Historical recordClass III

Great Lakes Cheese, Inc.

Product: Pasteurized Process Cheese Spread packaged under the followi…
Reason: Refrigerated pasteurized process cheese products may not be refrigerated at customer level due to labeled refrigeration requirements varying on finished product labels.
Published: September 27, 2023
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: January 10, 2025Historical recordClass III

Great Lakes Cheese, Inc.

Product: giant eagle Easy Melt, Pasteurized Prepared Cheese Spread.…
Reason: Refrigerated pasteurized process cheese products may not be refrigerated at customer level due to labeled refrigeration requirements varying on finished product labels.
Published: September 27, 2023
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: January 10, 2025Historical recordClass III

Great Lakes Cheese, Inc.

Product: Cheese Spread Pasteurized Process packaged under the followi…
Reason: Refrigerated pasteurized process cheese products may not be refrigerated at customer level due to labeled refrigeration requirements varying on finished product labels.
Published: September 27, 2023
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: February 10, 2025Historical recordClass II

Mount Franklin Foods LLC DBA Azar Nut Co.

Product: 1. 7 Select Cashews Halves & Pieces Honey Roasted, Net Wt 3…
Reason: Potential to contain undeclared soy and/or wheat allergen due to mislabeling.
Published: September 27, 2023
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: February 10, 2025Historical recordClass II

Mount Franklin Foods LLC DBA Azar Nut Co.

Product: Circle K Honey Roasted Peanuts, Net Wt 2.5 oz, UPC 194283102…
Reason: Potential to contain undeclared soy and/or wheat allergen due to mislabeling.
Published: September 27, 2023
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: February 10, 2025Historical recordClass II

Mount Franklin Foods LLC DBA Azar Nut Co.

Product: 1. Circle K Get Up Trail Mix, Net Wt 2 oz, UPC 194283102893…
Reason: Potential to contain undeclared soy and/or wheat allergen due to mislabeling.
Published: September 27, 2023
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: February 10, 2025Historical recordClass II

Mount Franklin Foods LLC DBA Azar Nut Co.

Product: Circle K Sweet & Spicy Mix, Net Wt 7 oz; UPC 194283104613
Reason: Potential to contain undeclared soy and/or wheat allergen due to mislabeling.
Published: September 27, 2023
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: February 10, 2025Historical recordClass II

Mount Franklin Foods LLC DBA Azar Nut Co.

Product: Power Snacks Honey Roasted Sunflower Kernels, Net Wt 1 oz; U…
Reason: Potential to contain undeclared soy and/or wheat allergen due to mislabeling.
Published: September 27, 2023
Distribution: Nationwide

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FDA Recall TerminatedTerminated: April 30, 2026Historical recordClass I

WEFUN Capsules 825 mg, 1x10 blister pack per carton, Manufactured by WEFUN Brooklyn NY 11204 www.eshoponlineusa.com Bar Code X00358V0O5

by Hua Da Trading, Inc. dba Wefun Inc.

Reason: Marketed Without an Approved NDA/ANDA: FDA analysis found the product to be tainted with sildenafil, an ingredient found in a FDA approved product for the treatment of male sexual enhancement, making this an unapproved drug.
Published: September 20, 2023
Distribution: Nationwide

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FDA Recall TerminatedTerminated: July 26, 2024Historical recordClass II

Sucralfate Oral Suspension 1g per 10mL, FOR ORAL ADMINISTRATION ONLY (414 mL bottle), Rx Only, Manufactured and Distributed by: VistaPharm, Inc. Largo, FL 33771, NDC 66689-305-16

by VistaPharm LLC

Reason: Superpotent/Subpotent single ingredient Drug: Out of Specification Assay results
Published: September 20, 2023
Distribution: Nationwide

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FDA Recall TerminatedTerminated: April 8, 2025Historical recordClass II

Pantoprazole Sodium for Injection 40mg per vial, Single dose vials NDC 71839-122-01 Packaged as (a) 10 Single-dose vials, NDC 71839-122-10; (b) 25 Single-dose vials, NDC 71839-122-25; Rx Only, Mfd. in India for and Distributed by: BE Pharmaceuticals Inc. 203 New Edition Court Cary, NC 27511.

by BE PHARMACEUTICALS AG

Reason: Lack of Assurance of Sterility: Powder discoloration due to small crack in some vials.
Published: September 20, 2023
Distribution: Nationwide

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Data last updated: October 19, 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.