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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.

37,142
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,799
Class I recallsReasonable probability of serious health consequences
24,349
Class II recallsTemporary or medically reversible health consequences
2,891
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 recallhttps://www.fsis.usda.gov/recalls-alerts/fontanini-foods-llc-recalls-raw-frozen-pork-sausage-products-due-possible-foreignPublished September 25, 2026
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)

  • 1,527 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

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

Recalls by class
ClassRecalls
Class II24,349
Class I9,799
Class III2,891
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,349
Class I9,799
Class III2,891
Not Yet Classified1

Showing 12,421–12,440 of 18,028 recalls

FDA Recall United States Terminated Historical recordClass II

Schreiber Food International

Product
Ambrosia Quality Foods Brand 4/1 gallon Worcestershire Sauce…
Reason
Ambrosia brand 4/1 Gallon Worcestershire Sauce may contain undeclared peanuts.
Published
February 1, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

HCG (Chorionic Gonadotropin Lyopholized) II, 1000 unit vial, Rx only, Prepared by Town & Country, Compounding & Consultation Services, 106 Prospect St - 1st FL, Ridgewood, NJ 07459

by Town and Country Compounding and Consultation Services, LLC

Reason
Subpotent Drug: due to failed potency results of 74% (spec. 80-125%).
Published
January 25, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Donepezil Hydrochloride Tablets, 10 mg, packaged in a) 30-count bottles (NDC 0781-5275-31) and b) 1000-count bottles (NDC 0781-5275-10), Rx only, Manufactured in India by Sandoz Private Ltd for Sandoz Inc., Princeton, NJ 08540.

by Sandoz Inc

Reason
Subpotent Drug: out of specification results for assay test.
Published
January 25, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Clindamycin Phosphate and Benzoyl Peroxide Gel, 1.2%/5%, 45 g tubes, Rx Only, Manufactured by Perrigo, Yeruham, Israel, Distributed by Perrigo, Allegan, MI --- NDC 45802-736-84, UPC 345802736840

by L. Perrigo Company

Reason
Microbial Contamination of Non-Sterile Product; small number of tubes may include the presence of mold on the cap
Published
January 25, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Novacort Gel Sample Packets (2% hydrocortisone acetate, 1% pramoxine HCl), 10-count Carton of 1.0 g sample packets), NDC 69646-704-38 (10 ct. Carton of 1gm samples) / NDC 69646-704-01 (Individual 1gm Samples within Carton), Rx Only, Novum Pharma LLC, Chicago, IL 60654

by Novum Pharma, LLC

Reason
Subpotent Drug: Out of specification result for pramoxine hydrochloride
Published
January 25, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Pentasa (mesalamine) Controlled-Release Capsules, 250 mg, 240 count bottle, Rx only, Manufactured for Shire US Inc., Lexington, MA --- NDC 54092-189-81

by Shire PLC

Reason
Presence of Foreign Tablets/Capsules; 500 mg capsules were found in bottles labeled to contain 250 mg capsules
Published
January 25, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Risedronate Sodium Delayed-release Tablets, 35 mg, Once-a-Week, 1 tablet per blister (NDC 0093-5509-19), packaged in 4 blisters per carton (NDC 0093-5509-44), Rx only, TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454.

by Teva Pharmaceuticals USA

Reason
Failed Dissolution Specifications
Published
January 25, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Herr Foods, Inc.

Product
Dried Smoke Chipotle Flavored Kettle Cooked Potato Chips 2.…
Reason
Herrs Foods is announcing a product recall on Chipotle flavored Kettle Potato Chips under the Herrs and the Peddlers Pantry Brand, 2.0 oz. due to possible health risk. These products were flavored with Chipotle seasoning that contained a milk ingredient . The milk ingredient is being recalled due to a potential risk of Salmonella contamination.
Published
January 25, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Herr Foods, Inc.

Product
Smoked Chipotle Flavored Kettle Cooked Potato Chips 2.625 o…
Reason
Herrs Foods is announcing a product recall on Chipotle flavored Kettle Potato Chips under the Herrs and the Peddlers Pantry Brand, 2.625 oz., and 8.0 oz. due to possible health risk. These products were flavored with Chipotle seasoning that contained a milk ingredient. The milk ingredient is being recalled due to a potential risk of Salmonella contamination.
Published
January 25, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Daytrana (methylphenidate transdermal system) Transdermal Patch, 30 mg over 9 hours (3.3 mg/hr), packaged in 30-count patches per box, Rx only, Manufactured by Noven Therapeutics, LLC, Miami, FL 33186; By Noven Pharmaceuticals, Inc., Miami, FL 33186, NDC 68968-5555-3.

by Noven Pharmaceuticals, Inc.

Reason
Defective Delivery System: Out of Specification (OOS) results for the mechanical peel force (MPF) and and/or the z-statistic values.
Published
January 18, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Daytrana (methylphenidate transdermal system) Transdermal Patch, 20 mg over 9 hours (2.2 mg/hr), packaged in 30-count patches per box, Rx only, Manufactured by Noven Therapeutics, LLC, Miami, FL 33186; By Noven Pharmaceuticals, Inc., Miami, FL 33186, NDC 68968-5554-3.

by Noven Pharmaceuticals, Inc.

Reason
Defective Delivery System: Out of Specification (OOS) results for the mechanical peel force (MPF) and and/or the z-statistic values.
Published
January 18, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Daytrana (methylphenidate transdermal system) Transdermal Patch, 10 mg over 9 hours (1.1mg/hr), packaged in- 30 count per box, Rx only, Manufactured by Noven Therapeutics, LLC, Miami, FL 33186; By Noven Pharmaceuticals, Inc, Miami, FL 33186, NDC 68968-5552-3

by Noven Pharmaceuticals, Inc.

Reason
Defective Delivery System: Out of Specification (OOS) results for the mechanical peel force (MPF) and and/or the z-statistic values.
Published
January 18, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Cytotec (misoprostol) Tablets, 200 mcg, 100 Tablets blister pack (10X10), For in-institution use only, Rx only, Distributed by G.D. Searle, Division of Pfizer, Inc., NY, NY --- NDC 0025-1461-34

by Pfizer Inc.

Reason
Failed Impurities/Degradations Specifications; Out of specification results for two known degradation products and total impurities at 18 months
Published
January 18, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Williams-Sonoma

Product
Williams-Sonoma Meyer Lemon Poppy Quick bread mix, NET WT. 1…
Reason
Williams Sonoma was notified by their contract manufacturer that high heat non fat dry milk powder that is now under recall for Salmonella was used in production of one of their quick bread mixes.
Published
January 18, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

All American Seasonings, Inc.

Product
Super Nacho (No-Pho, Gluten Free). Product Code: T4034. 50 l…
Reason
Products have been recalled due to potential for Salmonella contamination.
Published
January 18, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

All American Seasonings, Inc.

Product
Xtra Sharp Cheese Sauce. Product Code: T4015. 37.5 lb bags
Reason
Products have been recalled due to potential for Salmonella contamination.
Published
January 18, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

All American Seasonings, Inc.

Product
Triple Cheese Blend - No Color. Product Code: T4008. 50 lb b…
Reason
Products have been recalled due to potential for Salmonella contamination.
Published
January 18, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

All American Seasonings, Inc.

Product
Chedder and Sour Cream ASI. Product Code: T3937. 33 lb bags
Reason
Products have been recalled due to potential for Salmonella contamination.
Published
January 18, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

All American Seasonings, Inc.

Product
Jalapeno Popper ASI. Product Code: T3934. 33 lb bags
Reason
Products have been recalled due to potential for Salmonella contamination.
Published
January 18, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

All American Seasonings, Inc.

Product
French Onion Seasoning ASI. Product Code: T3933. 33 lb bags
Reason
Products have been recalled due to potential for Salmonella contamination.
Published
January 18, 2017
Distribution
Nationwide

View recall →

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.