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Recall totals

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

37,205

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,841

Class I recallsReasonable probability of serious health consequences

24,366

Class II recallsTemporary or medically reversible health consequences

2,892

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/gias-foods-inc-recalls-bettergoods-authentic-italian-lemon-alfredo-fettuccine-because-possible-0Published October 1, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated October 2, 2026 ET

Summary (Year to date)

1,714 recalls have been announced year to date.
Sep 2026 was 3% higher than the previous complete period (Aug 2026: 182).
The highest complete period was Jun 2026 (297).
Oct 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,366
Class I	9,841
Class III	2,892
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,366
Class I	9,841
Class III	2,892
Not Yet Classified	2

FDA Recall United States Terminated Historical recordClass II

Pharmavite

Product: Nature Made(R) D3 1000IU, 300 count, UPC 0-31604-02683-7
Reason: Specific lots of Nature Made(R) Vitamin D tablets may exceed specifications for yeast/mold.
Published: September 14, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Pharmavite

Product: Nature Made(R) adult gummies Hair.Skin.Nails, 90 count, UPC…
Reason: Specific lots of Nature Made(R) adult gummies Hair.Skin.Nails may exceed specifications total viable plate count.
Published: September 14, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Schulze & Burch Biscuit Co

Product: Aldi's Millville protein chew bars, peanut, dark chocolate &…
Reason: A supplier of one of the ingredients in the protein chewy bars informed firm of Listeria Monocytogenes positive.
Published: September 14, 2016
Distribution: The product was shipped to Aldi Inc. , 1…

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FDA Recall United States Terminated Historical recordClass II

Pharmavite

Product: Nature Made(R) adult gummies Multi, 150 count, UPC 0-31604-0…
Reason: Specific lots of Nature Made(R) product may have possible Salmonella contamination.
Published: September 14, 2016
Distribution: Nationwide

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FDA Recall United States Completed Historical recordClass II

Geneva Foods, LLC

Product: Lysander's All Natural Spicy Bourbon Flavor Rub; for beef, c…
Reason: Product contains undeclared allergens soy and wheat. Also does not declare sulfites.
Published: September 14, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Pharmavite

Product: Nature Made (R) Super B-Complex, KEY B VITAMINS + VITAMIN C,…
Reason: Lot No. 1173146, exp. JUL 2017 of Nature Made(R) product may have possible Staphylococcus aureus contamination. Lot No 1204001, exp. MAR 2018 of Nature Made(R) product may have possible Salmonella contamination.
Published: September 14, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Pharmavite

Product: Nature Made(R) Super B-Complex, KEY B VITAMINS + VITAMIN C,…
Reason: Specific lots of Nature Made(R) product may have possible Staphylococcus aureus contamination.
Published: September 14, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Pharmavite

Product: Nature Made(R) D3 1000IU, 125 count, UPC 0-31604-02793-3
Reason: Specific lots of Nature Made(R) Vitamin D tablets may exceed specifications for yeast/mold.
Published: September 14, 2016
Distribution: Nationwide

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FDA Recall United States Completed Historical recordClass II

Geneva Foods, LLC

Product: Lysander's Premium Teriyaki Marinade, 1 oz (28 g), polypropy…
Reason: Product contains undeclared allergens soy and wheat. Also does not declare sulfites.
Published: September 14, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Schnucks Markets Corporate Office

Product: Maytag Blue cheese cut and wrapped in clear plastic wrap at…
Reason: Product may be contaminated with Listeria monocytogenes.
Published: September 14, 2016
Distribution: Product was distributed to MO, IL, and I…

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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. 20714-48241-1, 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

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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. 20714-47478-2, 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

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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. 20714-47477-5, 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

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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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Data last updated: October 2, 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.