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Research historical outbreak investigations and the full recall archive, with charts, trends, and advanced filters. Looking for what's happening right now instead? See current Health Alerts.

Recall totals

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

37,204
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
Most affected stateHawaii 200 recalls mention this state

Download matching recalls as CSV

CSV exports include up to 5,000 matching rows (applying your current filters), not the full dataset if it's larger.

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Recalls announced by month (Year to date)

A chart of recalls grouped by month.

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Source: FDA and USDA public dataLast updated

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).
Recalls by class

A bar chart of the total number of recalls in this dataset by recall class.

Recalls by class
ClassRecalls
Class II24,366
Class I9,841
Class III2,892
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,366
Class I9,841
Class III2,892
Not Yet Classified2

Showing 12,461–12,480 of 19,967 recalls

FDA Recall United States Terminated Historical recordClass I

CFS West Holdings Inc

Product
BBQ Sauce, 200/0.88 oz Net Wt 11 lbs, Packed exclusively for…
Reason
Products potentially contain undeclared egg.
Published
November 22, 2017
Distribution
Product distributed to distributors in A…

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FDA Recall United States Terminated Historical recordClass I

CFS West Holdings Inc

Product
West Creek Original BBQ Sauce, Net Contents 1 Gal, Distribut…
Reason
Products potentially contain undeclared egg.
Published
November 22, 2017
Distribution
Product distributed to distributors in A…

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FDA Recall United States Terminated Historical recordClass I

CFS West Holdings Inc

Product
West Creek Sweet BBQ Sauce, Net Contents 1 Gal, Distributed…
Reason
Products potentially contain undeclared egg.
Published
November 22, 2017
Distribution
Product distributed to distributors in A…

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FDA Recall United States Terminated Historical recordClass I

CFS West Holdings Inc

Product
Monarch Worcestershire Sauce, Net 1 gallon, Distributed by U…
Reason
Products potentially contain undeclared egg.
Published
November 22, 2017
Distribution
Product distributed to distributors in A…

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FDA Recall United States Terminated Historical recordClass I

doTERRA International, LLC

Product
Slim & Sassy¿ TrimShake Vanilla, SKU 35180001, 1 lb 5.9 oz,…
Reason
doTERRA is voluntarily recalling unexpired Slim & Sassy¿ TrimShake - Chocolate and Slim & Sassy¿ TrimShake Vanilla mixes due to an undeclared milk allergen.
Published
November 22, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

CFS West Holdings Inc

Product
Texas Roadhouse Barbecue Sauce, NET 3/2 gallon, Mfg. exclusi…
Reason
Products potentially contain undeclared egg.
Published
November 22, 2017
Distribution
Product distributed to distributors in A…

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FDA Recall United States Terminated Historical recordClass II

Ruckers Makin Batch Candies

Product
dark chocolate peanuts, 8.5 oz.
Reason
Rucker s Wholesale & Service Co . initiated a voluntary recall on 10/31/2017 of Uncle Buck's and Family Choice Dark Chocolate Peanuts following a supplier's recall due to undeclared allergen milk.
Published
November 22, 2017
Distribution
Domestic: AL AZ CA CO IA ID IL LA…

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FDA Recall United States Terminated Historical recordClass II

Aurora Products, Inc.

Product
Dark Chocolate Turbinado Almonds w/ Sea Salt packaged in :…
Reason
Product contains undeclared milk
Published
November 22, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Aurora Products, Inc.

Product
Dark Chocolate Coffee beans packaged in Bulk 4 oz. Plasti…
Reason
Product contains undeclared milk
Published
November 22, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Aurora Products, Inc.

Product
Dark Chocolate Cranberries packaged in: Bulk 3.5 oz. Pl…
Reason
Product contains undeclared milk
Published
November 22, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Aurora Products, Inc.

Product
Aurora Brand Dark Chocolate Cherries packaged in: 8.5 oz.…
Reason
Product contains undeclared milk
Published
November 22, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Aurora Products, Inc.

Product
Dark Chocolate Almonds packaged in: 4 oz. Plastic Pouch,…
Reason
Product contains undeclared milk
Published
November 22, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Doan's Pain Relieving Cream with 4% Lidocaine Plus Menthol, (lidocaine 4%, menthol 1%), Net Wt. 2.75 oz. (77.3 g) Tube, Distributed by: Ducere Pharma, LLC New Hope, PA 18938 USA --- UPC 849648000023

by Dr. Reddy's Laboratories, Inc.

Reason
Labeling: Incorrect or Missing Lot and/or Exp Date; lot number on the secondary packaging doesnt match the lot number printed on the bottle
Published
November 15, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Betadine Solution Swabstick Povidone-Iodine Solution USP, 10% Dist.by: Purdue Products LP. Stamford, CT 06901-3431 NDC 67618-153-01

by Purdue Pharma, LP

Reason
Subpotent Drug: The laminate used to make the pouches was reversed such that the aluminum layer was in contact with the product causing an exothermic reaction between the free iodine and the aluminum.
Published
November 15, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

21ST CENTURY SNACK FOODS

Product
21st CENTURY SNACK FOODS DARK CHOCOLATE ALMONDS Roasted Almo…
Reason
Product contains undeclared milk.
Published
November 15, 2017
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

Stonyfield Farm

Product
Stonyfield ORGANIC O'soy Strawberry on the bottom SOY YOGURT…
Reason
Product may contain undeclared milk.
Published
November 15, 2017
Distribution
Multiple states

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FDA Recall Terminated Historical recordClass II

Dutasteride and Tamsulosin HCl Capsules, 0.5 mg/ 0.4 mg, packaged in a) 30-count bottle (NDC 0591-3771-30), b) 90-count bottle (NDC 0591-3771-19), Rx only, Manufactured by: Actavis Laboratories FL, Inc. Fort Lauderdale, FL 33314 USA; Distributed by: Actavis Pharma, Inc. Parsippany, NJ 07054 USA.

by Teva Pharmaceuticals USA

Reason
Failed dissolution specifications; all lots within expiry are being recalled due to out of specification dissolution results.
Published
November 8, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

ROCuronium Bromide 10 mg per mL, 5 mL Fill in single dose syringe, (50 mg / 5 mL Total Dose) Rx Only SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205, NDC 70004-850-09

by SCA Pharmaceuticals, LLC

Reason
Lack Of Assurance Of Sterility.
Published
November 8, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Calcium GLUCOnate 2 g added to 0.9% Sodium Chloride 50 mL Bag, Each bag contains 9.3 mEq Ca++ Rx Only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205, NDC 70004-0510-30

by SCA Pharmaceuticals, LLC

Reason
Lack Of Assurance Of Sterility.
Published
November 8, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

PHENYLephrine HCl 100 mcg per mL In 0.9% Sodium Chloride 10 mL Fill Volume in a Single Dose Syringe (1,000 mcg / 10 ml Total Dose), Rx Only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR, NDC 70004-0810-12

by SCA Pharmaceuticals, LLC

Reason
Lack Of Assurance Of Sterility.
Published
November 8, 2017
Distribution
Nationwide

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Data last updated:

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.