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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: WA ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated October 18, 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

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

FDA Recall United States TerminatedTerminated: November 26, 2024Historical recordClass III

Lemonland Food Corp

Product: Item FLD1004A, Seasoned Dried Whiting, distributed in plasti…
Reason: Soybean Sauce is declared but Wheat is not declared.
Published: October 23, 2024
Distribution: Distributed in WA

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FDA Recall United States TerminatedTerminated: November 26, 2024Historical recordClass I

Lemonland Food Corp

Product: Item FLD1000BA, Perilla Leaves in Soy Sauce, distributed in…
Reason: Soybean Sauce is declared but Wheat and Fish (Anchovy) are not declared.
Published: October 23, 2024
Distribution: Distributed in WA

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FDA Recall United States TerminatedTerminated: November 26, 2024Historical recordClass III

Lemonland Food Corp

Product: Item FLD1000AA, Seasoned Sesame Leaves or Seasoned Perilla L…
Reason: Undeclared Monosodium Glutamate
Published: October 23, 2024
Distribution: Distributed in WA

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FDA Recall United States TerminatedTerminated: November 26, 2024Historical recordClass II

Lemonland Food Corp

Product: Item FLD1000A, Perilla Leaves in Soybean Paste, distributed…
Reason: Soybean Paste is declared but Wheat and Sesame Seeds are not declared.
Published: October 23, 2024
Distribution: Distributed in WA

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FDA Recall United States TerminatedTerminated: November 26, 2024Historical recordClass I

Lemonland Food Corp

Product: Item FLD4006, Potato Salad, distributed in plastic clamshell…
Reason: Mayonnaise is declared but Soybean Oil and Egg are not declared.
Published: October 23, 2024
Distribution: Distributed in WA

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FDA Recall United States TerminatedTerminated: February 11, 2025Historical recordClass I

Nuts.com

Product: S'mores Bites, 1 yummy pound, Distributed by Nuts.com, Cranf…
Reason: Undeclared Allergen, milk - a mix-up between the product description and the ingredient list. Milk Chocolate was listed in the product description but was missing from the ingredient list.
Published: October 23, 2024
Distribution: The adulterated product was distributed…

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FDA Recall United States TerminatedTerminated: June 23, 2025Historical recordClass II

Hydration Labs Inc. dba Bevi

Product: Flavor#115 Electrolytes, Net Contents 3.78L, #740-0115, GTIN…
Reason: Product is labeled as electrolytes but is actually caffeine
Published: October 23, 2024
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: January 29, 2025Historical recordClass III

Walmart Inc

Product: Great Value Cherry Mixed Fruit, 4 oz, 4 Count and 12 count p…
Reason: FD&C Red No 3 was not declared as an ingredient.
Published: October 23, 2024
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: January 29, 2025Historical recordClass III

Walmart Inc

Product: Great Value Diced Peaches, Mandarin Segments, & Cherry Mixed…
Reason: FD&C Red No 3 was not declared as an ingredient.
Published: October 23, 2024
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: November 7, 2024Historical recordClass II

Pacific Coast Fresh CO

Product: King Harvest Spinach Hummus, perishable and refrigerated, pa…
Reason: Recall initiated due to potential plastic fragments.
Published: October 23, 2024
Distribution: Distributed in OR and WA.

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FDA Recall OngoingHistorical recordClass II

Ryaltris (olopatadine hydrochloride and mometasone fluorate) Nasal Spray, 665 mcg/25 mcg per spray, 240 Metered Sprays/bottle, 29 g net fill weight, Distr. by Hikma Specialty USA Inc., Columbus, OH 43328, hikma, Glenmark Specialty SA. NDC 59467-700-27.

by Glenmark Pharmaceuticals Inc., USA

Reason: Defective Delivery System: The dip tube is clogged causing the spray not to work.
Published: October 9, 2024
Distribution: Nationwide

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FDA Recall TerminatedTerminated: July 29, 2025Historical recordClass I

Veklury (remdesivir) for injection, 100 mg/vial, Single-Dose Vial, Rx only, Manufactured for: Gilead Sciences, Inc., Foster City, CA 94404, NDC 61958-2901-2

by Gilead Sciences, Inc.

Reason: Presence of Particulate Matter: Presence of glass particle.
Published: October 9, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass I

Gold Hard Steel Plus Liquid, 2 FL OZ bottles, UPC 787188873199

by Supercore Products Group Inc.

Reason: Marketed without an approved NDA/ANDA: FDA analysis found products to be tainted with undeclared acetaminophen and sildenafil.
Published: October 9, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass I

Hard Steel Capsules packaged in 1 count blister packs in boxes of 10, 20 and 30, Manufactured in U.S.A.

by Supercore Products Group Inc.

Reason: Marketed without an approved NDA/ANDA: FDA analysis found products to be tainted with undeclared acetaminophen and sildenafil.
Published: October 9, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass III

Ciclopirox Gel 0.77%, For Dermatologic Use Only, Not for Use in Eyes, Rx Only, a) 30 gm Tube, NDC 68462-0455-35; b) 45 gm Tube, NDC 68462-0455-47; c) 100 gm Tube, NDC 68462-0455-94, Manufactured by: Glenmark Pharmaceuticals, Ltd., Colvale-Bardez, Goa 403513, India, Manufactured for: Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ 07430.

by Glenmark Pharmaceuticals Inc., USA

Reason: Defective Container: Firm received complaints of broken tube at the seal.
Published: October 9, 2024
Distribution: Nationwide

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FDA Recall TerminatedTerminated: July 1, 2026Historical recordClass II

Atorvastatin Calcium Tablets, USP, 40mg, Rx only, 1000 Tablets per bottle, Manufactured for: Nivagen Pharmaceuticals, Inc. Sacramento, CA 95827, USA, Manufactured by: Umedica Laboratories Pvt Ltd., Vapi Gujarat 396195, India, NDC: 75834-257-01.

by Nivagen Pharmaceuticals Inc

Reason: Presence of Foreign Tablets/Capsules: A Carbamazepine Extended-Release 400 mg tablet was found in a 1000-count bottle of Atorvastatin Calcium Tablets, USP 40 mg.
Published: October 9, 2024
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: October 24, 2024Historical recordClass II

Mac & Co

Product: Mini Raspberry Lemon Coffee Cake, net wt. 13.5oz. UPC 8 572…
Reason: Undeclared walnut and wheat. Mini Squash Harvest Loaf (UPC 8 55324 00505 3) was mis-labeled as Mini Raspberry Lemon Coffee Cake (UPC 8 57297 00745 4) and therefore wheat flour and walnuts are not declared on label.
Published: October 9, 2024
Distribution: Distributed in WA only

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FDA Recall United States TerminatedTerminated: December 13, 2024Historical recordClass II

Blue Tape Sriracha

Product: Blue Tape Sriracha sauce is refrigerated condiment, packaged…
Reason: Acidified product was manufactured by firm without ODA license.
Published: October 9, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Mycophenolic Acid Delayed-Release Tablets USP, 360 mg, Rx Only, 120 Tablets per bottle, Manufactured by Alkem Laboratories, LTD, INDIA; Distributed by Ascend Laboratories, LLC, Parsippany, NJ 07054, NDC 67877-427-12.

by Ascend Laboratories, LLC

Reason: Failed Dissolution Specifications
Published: October 2, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Infla-650 Herbal Dietary Supplement, 700mg, packaged in pouches containing 60 capsules, Distributed by: Guru Inc., 4370 Lawrenceville Hwy NW, P.O. Box 2204, Lilburn, GA 30047-1100, USA. Ph.: 872 216 1566, http://www.dalayurevda.com, Made in India, UPC: 042535355019

by Guru Inc.

Reason: Marketed without an approved NDA/ANDA: FDA analysis found product to be tainted with undeclared acetaminophen, diclofenac, and phenylbutazone.
Published: October 2, 2024
Distribution: Nationwide

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Data last updated: October 18, 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.