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Recall totals

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

37,118

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,793

Class I recallsReasonable probability of serious health consequences

24,343

Class II recallsTemporary or medically reversible health consequences

2,887

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/gf-blends-recalls-truly-aip-all-purpose-flour-and-bread-mix-and-eat-gangster-flat-bread-pizza-mixPublished September 18, 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 September 22, 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	24,343
Class I	9,793
Class III	2,887
Not Yet Classified	1

Recalls by class
Class	Recalls
Class II	24,343
Class I	9,793
Class III	2,887
Not Yet Classified	1

FDA Recall United States Terminated Historical recordClass II

Olive Bakery

Product: Peanut Butter bread packages contain two bread pastries fill…
Reason: Label declares flour but does not declare wheat. Product contains Non-Dairy Cream but label does not declare this sub-ingredient Soy Lecithin.
Published: September 4, 2019
Distribution: distributed in OR and WA

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FDA Recall United States Terminated Historical recordClass II

Olive Bakery

Product: Cream Horns packages contain one bread pastry filled with no…
Reason: Label declares flour but does not declare wheat. Label declares Non-Dairy Whipped Cream but does not declare its sub-ingredients Soy Lecithin.
Published: September 4, 2019
Distribution: distributed in OR and WA

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FDA Recall United States Terminated Historical recordClass II

Olive Bakery

Product: Bavarian bread packages contain two bread pastries filled wi…
Reason: Label declares flour but does not declare wheat. Product contains Non-Dairy Cream but label does not declare this sub-ingredient Soy Lecithin.
Published: September 4, 2019
Distribution: distributed in OR and WA

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FDA Recall United States Terminated Historical recordClass II

Olive Bakery

Product: Mocha Cream bread packages contain two bread pastries and ea…
Reason: Label declares flour but does not declare wheat. Almond is visible through a clear package but label does not declare almond. Product also contains Non-Dairy Cream but label does not declare this sub-ingredient Soy Lecithin.
Published: September 4, 2019
Distribution: distributed in OR and WA

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FDA Recall United States Terminated Historical recordClass II

Olive Bakery

Product: Cream bread packages contain two bread pastries filled with…
Reason: Label declares flour but does not declare wheat. Product contains Non-Dairy Cream but label does not declare this sub-ingredient Soy Lecithin.
Published: September 4, 2019
Distribution: distributed in OR and WA

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FDA Recall United States Terminated Historical recordClass II

Olive Bakery

Product: Peanut Crunch bread packages contain two bread pastries with…
Reason: Label declares flour but does not declare wheat.
Published: September 4, 2019
Distribution: distributed in OR and WA

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FDA Recall United States Terminated Historical recordClass II

Olive Bakery

Product: White Bean bread is filled with white bean paste filling an…
Reason: Label declares flour but does not declare wheat.
Published: September 4, 2019
Distribution: distributed in OR and WA

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FDA Recall United States Terminated Historical recordClass II

Olive Bakery

Product: Green Bean bread topped with black sesame seeds, packaged to…
Reason: Label declares flour but does not declare wheat.
Published: September 4, 2019
Distribution: distributed in OR and WA

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FDA Recall United States Terminated Historical recordClass II

Olive Bakery

Product: Red Bean bread package contains two bread pastries filled wi…
Reason: Label declares flour but does not declare wheat.
Published: September 4, 2019
Distribution: distributed in OR and WA

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FDA Recall United States Terminated Historical recordClass II

PreGel America, Inc.

Product: PreGel Lemon 50 4.4 lb (2kg) bag, Ingredients: dextrose, cit…
Reason: Undeclared Milk. The firm received a complaint that there was milk in the product. The product ingredient statement does not include milk.
Published: September 4, 2019
Distribution: Product was shipped to the following sta…

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FDA Recall United States Terminated Historical recordClass II

AWERS Inc

Product: Grained Salmon Caviar 95g (Sockeye Salmon Caviar), refrigera…
Reason: Grained salmon caviar, refrigerated, was recalled due to a potential to be contaminated with Clostridium botulinum.
Published: September 4, 2019
Distribution: Distributed in California, New York, Ore…

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FDA Recall United States Terminated Historical recordClass II

WHOLE FOODS MARKET

Product: 365 Organic Maple & Brown Sugar Pecan Instant Oatmeal 2.3 o…
Reason: Undeclared pecans
Published: September 4, 2019
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass II

Confectionery Arts International, LLC

Product: All colors and sizes of Confectionery Arts International, LL…
Reason: Borosilicate glass material found in FDA Sample.
Published: September 4, 2019
Distribution: Distributed in 26 states: NC, IN, KY, FL…

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FDA Recall Terminated Historical recordClass II

Ketamine 50 mg/5 mL in 0.9% Sodium Chloride Injection for IV or IM Use (concentration = 10 mg/mL), 6 mL Syringe, Rx Only, SCA Pharmaceuticals, Windsor, CT 06095, NDC 70004-0430-09.

by SCA Pharmaceuticals, LLC

Reason: Lack of Assurance of Sterility.
Published: August 28, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Clear Eyes Redness Relief Hand Pocket Pal Tray Display; each display (UPC 6 78112 25418 7) contains 48 each of Clear eyes REDNESS RELIEF (Glycerin 0.25%, Naphazoline hydrochloride 0.012%) eye drops, 0.2 FL OZ (6 mL) bottle, Handy Pocket Pal (UPC 6 78112 25418 7); Distributed by Medtech Products Inc., Tarrytown, NY 10591 A Prestige Brands Company.

by Medtech Products, Inc.

Reason: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance controls over critical systems in the manufacturing facility that could impact the product quality of the finished products.
Published: August 28, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Clear eyes REDNESS RELIEF (Glycerin 0.25%, Naphazoline hydrochloride 0.012%) eye drops, Handy Pocket Pal, 0.2 FL OZ (6 mL) bottle, Distributed by Select Corporation, Carrolton, TX 75007; Medtech Products Inc., Tarrytown, NY 10591, A Prestige Brands Company, UPC 6 55708 01039 6.

by Medtech Products, Inc.

Reason: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance controls over critical systems in the manufacturing facility that could impact the product quality of the finished products.
Published: August 28, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Clear Eyes Redness Relief Handy Pocket Pal Club Pak Display; each display (case UPC 30300742541283) contains 48 each of Clear eyes REDNESS RELIEF (Glycerin 0.25%, Naphazoline hydrochloride 0.012%) eye drops, 0.2 FL OZ (6 mL) bottle, Handy Pocket Pal (UPC 6 78112 25418 7); Distributed by Medtech Products Inc., Tarrytown, NY 10591; A Prestige Brands Company.

by Medtech Products, Inc.

Reason: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance controls over critical systems in the manufacturing facility that could impact the product quality of the finished products.
Published: August 28, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Clear Eyes Maximum Itchy Eye Relief Sidekick Floor Stand Display; each display (case UPC 10678112736383) contains 12 each of Clear eyes MAXIMUM ITCHY EYE RELIEF (Glycerin 0.25%, Naphazoline hydrochloride 0.012%, Zinc Sulfate 0.25%) eye drops, 0.5 FL OZ (15 mL) bottle, (UPC 6 78112 65920 3), Distributed by Medtech Products Inc., Tarrytown, NY 10591, A Prestige Brands Company.

by Medtech Products, Inc.

Reason: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance controls over critical systems in the manufacturing facility that could impact the product quality of the finished products.
Published: August 28, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Clear Eyes Maximum Redness Relief Club Pack Display; each display contains 18 3-Pack bottles (UPC 6 78112 10859 6) of Clear eyes MAXIMUM REDNESS RELIEF (Glycerin 0.5%, Naphazoline hydrochloride 0.03%) eye drops, 0.5 FL OZ (15 mL) bottle, (UPC 6 78112 66577 8); Distributed by Medtech Products Inc., Tarrytown, NY 10591, A Prestige Brands Company.

by Medtech Products, Inc.

Reason: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance controls over critical systems in the manufacturing facility that could impact the product quality of the finished products.
Published: August 28, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Clear Eyes Maximum Itchy Eye Relief Sidekick Floor Stand Display; each display contains 12 each of Clear eyes MAXIMUM ITCHY EYE RELIEF (Glycerin 0.25%, Naphazoline hydrochloride 0.012%, Zinc Sulfate 0.25%) eye drops, 0.5 FL OZ (15 mL) bottle, (UPC 6 78112 65920 30; Distributed by Medtech Products Inc., Tarrytown, NY 10591, A Prestige Brands Company, case UPC 10678112106995.

by Medtech Products, Inc.

Reason: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance controls over critical systems in the manufacturing facility that could impact the product quality of the finished products.
Published: August 28, 2019
Distribution: Nationwide

View recall →

Data last updated: September 22, 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.