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Recall totals

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

37,223

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,844

Class I recallsReasonable probability of serious health consequences

24,370

Class II recallsTemporary or medically reversible health consequences

2,896

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 2,073 recalls

Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/frutas-y-hortalizas-del-sur-sa-expands-recalls-include-additional-lots-great-value-frozen-organicPublished October 2, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated October 6, 2026 ET

Summary (Year to date)

1,725 recalls have been announced year to date.
Sep 2026 was 7% 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	24,370
Class I	9,844
Class III	2,896
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,370
Class I	9,844
Class III	2,896
Not Yet Classified	2

FDA Recall Terminated Historical recordClass III

CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15, 1 FL. OZ.LIQ./30 ml bottle within a carton, Clinique Labs., Dist. New York, N.Y., 10022; New York, London W1K 3BQ; Paris, UPC No. 20714-48241-1, Shade 06 (D-G)

by Clinique International

Reason: Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and octisalate, are below the specifications for assay.
Published: September 7, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15, 1 FL. OZ.LIQ./30 ml bottle within a carton, Clinique Labs., Dist. New York, N.Y., 10022; New York, London W1K 3BQ; Paris, UPC No. 20714-48240-4, Shade 05 (D-G)

by Clinique International

Reason: Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and octisalate, are below the specifications for assay.
Published: September 7, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15, 1 FL. OZ.LIQ./30 ml bottle within a carton, Clinique Labs., Dist. New York, N.Y., 10022; New York, London W1K 3BQ; Paris, UPC No. 20714-47479-9, Shade 04 (M-N)

by Clinique International

Reason: Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and octisalate, are below the specifications for assay.
Published: September 7, 2016
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15, 1 FL. OZ.LIQ./30 ml bottle within a carton, Clinique Labs., Dist. New York, N.Y., 10022; New York, London W1K 3BQ; Paris, UPC No. 20714-47478-2, Shade 03 (MF-N)

by Clinique International

Reason: Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and octisalate, are below the specifications for assay.
Published: September 7, 2016
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15, 1 FL. OZ.LIQ./30 ml bottle within a carton, Clinique Labs., Dist. New York, N.Y., 10022; New York, London W1K 3BQ; Paris, UPC No. 20714-47477-5, Shade 02 (VF-N)

by Clinique International

Reason: Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and octisalate, are below the specifications for assay.
Published: September 7, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15, 1 FL. OZ.LIQ./30 ml bottle within a carton, Clinique Labs., Dist. New York, N.Y., 10022; New York, London W1K 3BQ; Paris, UPC No. 20714-47476-8, Shade 01 (VF-N)

by Clinique International

Reason: Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and octisalate, are below the specifications for assay.
Published: September 7, 2016
Distribution: Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

Hampton Creek Foods

Product: JUST Blueberry Muffin Mix; NET WT 23.3 oz. (1 lb 7.3 oz) 66…
Reason: Firm received a positive test result for Salmonella in Coconut Milk powder which was used in the manufacturing on six cake and muffin mixes.
Published: September 7, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

International Foodsource, LLC

Product: IFS Web Bulk Pistachio Raw Shelled 80% Wholes Net Wt. 30 lb.…
Reason: Raw pistachios may be contaminated with Salmonella which was determined through FDA contract laboratory testing.
Published: September 7, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Eastland Food Corporation

Product: Euro Custard Cake, Plastic wrapped cardboard container (Net…
Reason: The New York Department of Agriculture and Markets tested the Euro Custard Cake an detected that the product contained milk. The label did not declare milk and list it as an allergen on the label. Eastland Food Corporation became aware of these results on June 21 when FDA visited it facility. Eastland Food Corporation performed an investigation into the matter and determine late on June 22 that a single lot (310 cases) of product was missing this information. To this point no adverse incidents have been reported due to the mislabeling. Health risk assessment, people who have an allergy or severe sensitivity to milk run the risk of a serious or life threatening allergic reaction if they consume the affected Euro Custard Cakes under the mistaken assumption that it does not contain milk.
Published: September 7, 2016
Distribution: The cases in the lot were distributed to…

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FDA Recall United States Terminated Historical recordClass I

Hampton Creek Foods

Product: JUST Yellow Cake Mix; NET WT 20 z. (1 lb 4oz) 567 g); UPC…
Reason: Firm received a positive test result for Salmonella in Coconut Milk powder which was used in the manufacturing on six cake and muffin mixes.
Published: September 7, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Hampton Creek Foods

Product: JUST Chocolate Chunk Muffin Mix; NET WT 20.8 oz. (1 lb 4.8…
Reason: Firm received a positive test result for Salmonella in Coconut Milk powder which was used in the manufacturing on six cake and muffin mixes.
Published: September 7, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Let's Do Lunch, Inc.

Product: Chicken Double Dogs on Whole Grain Bun Product ID 809021
Reason: Potential Listeria monocytogenes contamination.
Published: September 7, 2016
Distribution: U.S. distribution to the following; CA,…

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FDA Recall United States Terminated Historical recordClass II

Carfagnas Inc

Product: Carfagnas Spicy Chili Ready Sauce in 32 oz. glass jars.
Reason: Acidified process not on file with the FDA
Published: September 7, 2016
Distribution: Ohio only

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FDA Recall United States Terminated Historical recordClass I

J&D's Down Home Enterprises, Inc.

Product: Original Bacon Flavored Seasoning Salt, Big Pig brand, 16oz…
Reason: Original Bacon Flavored Seasoning Salt, Big Pig brand, is recalled due to a potential to be contaminated with E. coli O121.
Published: September 7, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Minnie Marie Bakers, Inc. dba Awrey's Bakery

Product: Deep Chocolate Sheet Cake 8x12 28.125 lb case 20, 22.5 o…
Reason: Products may contain undeclared tree nuts (walnuts). People who have an allergy or severe sensitivity to tree nuts run the risk of serious or life-threatening allergic reaction if they consume these products.
Published: September 7, 2016
Distribution: Ohio

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FDA Recall United States Terminated Historical recordClass I

Minnie Marie Bakers, Inc. dba Awrey's Bakery

Product: Chocolate Roll Cake 15x24 22 lb case 8, 2 lb 12 oz cakes…
Reason: Products may contain undeclared tree nuts (walnuts). People who have an allergy or severe sensitivity to tree nuts run the risk of serious or life-threatening allergic reaction if they consume these products.
Published: September 7, 2016
Distribution: Ohio

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FDA Recall United States Terminated Historical recordClass I

Let's Do Lunch, Inc.

Product: Chili Dog, Low Fat/Low Sodium Product ID 952000
Reason: Potential Listeria monocytogenes contamination.
Published: September 7, 2016
Distribution: U.S. distribution to the following; CA,…

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FDA Recall United States Terminated Historical recordClass I

Let's Do Lunch, Inc.

Product: All American Cheeseburger Product ID 470007
Reason: Potential Listeria monocytogenes contamination.
Published: September 7, 2016
Distribution: U.S. distribution to the following; CA,…

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FDA Recall United States Terminated Historical recordClass I

Let's Do Lunch, Inc.

Product: Chicken Patty Sandwich on a Whole Grain Bun Product ID 4000…
Reason: Potential Listeria monocytogenes contamination.
Published: September 7, 2016
Distribution: U.S. distribution to the following; CA,…

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FDA Recall United States Terminated Historical recordClass I

Let's Do Lunch, Inc.

Product: BBQ Rib Sandwich Product ID C46007, 460007
Reason: Potential Listeria monocytogenes contamination.
Published: September 7, 2016
Distribution: U.S. distribution to the following; CA,…

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Data last updated: October 6, 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.