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Recall totals

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

37,115

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/so-delicious-dairy-freer-issues-voluntary-recall-salted-caramel-cluster-non-dairy-frozen-dessertPublished September 15, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 16, 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

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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

Taylor Farms Northwest, LLC

Product: Taylor Farms Jicama Sticks, Refrigerated & Ready To Eat prod…
Reason: Metal fragment. A piece of metal about 3/4 inch was found in retail package.
Published: December 14, 2022
Distribution: Distributed in Washington only.

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FDA Recall United States Terminated Historical recordClass II

Betty Buzz LLC

Product: Betty Buzz Sparkling Grapefruit - Non-alcoholic Beverage & M…
Reason: Beverage has off-odor
Published: December 14, 2022
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Nestle-USA, Inc. (Corporate Office)

Product: Nestle Toll House Edible Chocolate Chip Cookie Dough package…
Reason: Potential of foreign material within product.
Published: December 14, 2022
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass I

GREEN DAY PRODUCE

Product: Enoki Mushroom Net wt. 200g (7.05 oz.) 25 units per case UPC…
Reason: Product found to be contaminated with Listeria monocytogenes
Published: December 14, 2022
Distribution: Product was distributed to 18 distributo…

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FDA Recall Terminated Historical recordClass III

Sodium Sulfacetamide 10% Sulfur 4% Cleansing Pads, Net weight 3.7g (60 cleansing pads Net weight 3.7 g each per carton,) Rx Only, Manufactured For: Acella Pharmaceuticals, LLC Alpharetta, GA 300025, NDC 42192-113-60

by Acella Pharmaceuticals, LLC

Reason: Subpotent drug: Out of specification for assay at the end-of-shelf-life 24-month period.
Published: December 7, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Allergy Relief D, Fexofenadine HCL 60mg/Antihistamine, Pseudoephedrine HCL 120mg/Nasal Decongestant, Extended-Release Tablets USP, packaged as (a) 20 count carton NDC 49032-273-20; (b) 30 count carton, NDC49032-273-30; Distributed by: Walmart Inc., Bentonville, AR 72716, Product of India

by Dr. Reddy's Laboratories, Inc.

Reason: Failed dissolution specifications
Published: December 7, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Desmopressin Acetate Tablets 0.2mg, 100-count bottles, RX Only, Distributed by: Avet Pharmaceuticals Inc. East Brunswick, NJ 08816, NDC 23155-490-01

by Heritage Pharmaceuticals Inc

Reason: Subpotent Drug
Published: December 7, 2022
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Daytrana (methylphenidate transdermal system), Delivers 15 mg over 9 hours, (1.6 mg/hr), 30 patches per box, Rx only, Manufactured for Noven Therapeutics, LLC, Miami, FL 33186; By Noven Pharmaceuticals, Inc., Miami, FL 33186, NDC 68968-5553-3.

by Noven Pharmaceuticals Inc

Reason: Defective Delivery System: Recalled lot was found to be out of specification for shear. Shear is an attribute related to the adhesive properties of the transdermal patches.
Published: December 7, 2022
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

fayeon distributors inc.

Product: Choi Heong Yuen Bakery Almond Cakes in round metal container…
Reason: Product may contain undeclared milk
Published: December 7, 2022
Distribution: A total of 20 customers received this pr…

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FDA Recall United States Terminated Historical recordClass II

Amys Kitchen Inc

Product: Amy's Kitchen Gluten Free Bean and Cheese Burrito 5.5 oz. in…
Reason: Product may contain foreign material: pieces of plastic
Published: December 7, 2022
Distribution: Product was distributed to the following…

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FDA Recall United States Terminated Historical recordClass III

Perfect Day Inc

Product: Coolhaus Dairy Free Cookie Dough Lyfe Frozen Dessert Sandwic…
Reason: Presence of coliform found in 3rd party lab samples
Published: December 7, 2022
Distribution: Product was shipped only to consignee, K…

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FDA Recall Terminated Historical recordClass III

Phenytoin Sodium Injection, USP, 250 mg/5 mL, NDC 42192-614-05, packaged in 10 x 5 mL vials per carton, NDC 42192-614-30, Rx only, Manufactured for: Acella Pharmaceuticals, LLC Alpharetta, GA 30005

by Acella Pharmaceuticals, LLC

Reason: Labeling: Not elsewhere classified; the product is being recalled because of customer complaints that the primary vial label was missing a barcode.
Published: November 30, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Phenytoin Sodium Injection, USP 100 mg/2 mL, NDC 42192-614-02, packaged in 10 x 2 mL vials per carton, NDC 42192-614-10, Rx only, Manufactured for: Acella Pharmaceuticals, LLC Alpharetta, GA 30005

by Acella Pharmaceuticals, LLC

Reason: Labeling: Not elsewhere classified; the product is being recalled because of customer complaints that the primary vial label was missing a barcode.
Published: November 30, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Pantoprazole Sodium for Delayed-Release Oral Suspension40 mg suspension in apple juice or applesauce only Each packet contains 40 mg pantoprazole equivalent to 45.1 mg of pantoprazole sodium USP (sesquihydrate), Rx Only, distributed by: Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512, manufactured by: Sun Pharmaceutical Industries Limited Mohali, INDIA, NDC 62756-071-60

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason: Discoloration
Published: November 30, 2022
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Sodexo, DBA Nourish

Product: Nourish Inc. brand Fruit Snack Pack SNACK ATTACK 6.48 oz. Ap…
Reason: Undeclared peanut allergen
Published: November 30, 2022
Distribution: Product was distributed to 4 customers,…

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FDA Recall United States Completed Historical recordClass I

Seed Ranch Flavor Co

Product: Everything But The Sushi & Dumplings, 5 fl. oz. (148 mL) gla…
Reason: Three sauces contain undeclared soy.
Published: November 30, 2022
Distribution: Nationwide

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FDA Recall United States Completed Historical recordClass I

Seed Ranch Flavor Co

Product: Umami Everyday Savory Spice, 5 fl. oz. (148 mL) glass bottle…
Reason: Three sauces contain undeclared soy.
Published: November 30, 2022
Distribution: Nationwide

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FDA Recall United States Completed Historical recordClass I

Seed Ranch Flavor Co

Product: Umami Everyday Sauce, 5 fl. oz. (148 mL) glass bottle, UPC 8…
Reason: Three sauces contain undeclared soy.
Published: November 30, 2022
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

DAISO CALIFORNIA WAREHOUSE

Product: Tiramisu Twist Cookie 3.4 oz. packaged in a gold bag with a…
Reason: Tiramisu Twist Cookies were found to have tree nuts not declared on the label
Published: November 30, 2022
Distribution: Product is distributed to Daiso retail l…

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FDA Recall United States Terminated Historical recordClass II

G FUEL LLC

Product: GFUEL brand Watermelon Limeade Energy Drink; 16 fl. oz.; rea…
Reason: Product label does not declare the correct amount of caffeine.
Published: November 30, 2022
Distribution: Nationwide

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Data last updated: September 16, 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.