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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 15,561–15,580 of 21,156 recalls

FDA Recall United States Terminated Historical recordClass I

Treehouse Foods

Product
UPC 4130300137, Essential Everyday Trail Mix Bars, Best By/…
Reason
TreeHouse Foods is recalling products that may be impacted by sunflower seeds contaminated with Listeria monocytogenes.
Published
October 12, 2016
Distribution
US: AL, AZ, AR, CA, CO, CT, FL, IL, IN,…

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FDA Recall United States Terminated Historical recordClass I

Treehouse Foods

Product
UPC 071725711533, Natures Harvest Southwest Trail MixBest By…
Reason
TreeHouse Foods is recalling products that may be impacted by sunflower seeds contaminated with Listeria monocytogenes.
Published
October 12, 2016
Distribution
US: AL, AZ, AR, CA, CO, CT, FL, IL, IN,…

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FDA Recall United States Terminated Historical recordClass I

Treehouse Foods

Product
UPC 071725714688, Raisin and Nut Trail Mix, Best By/Date Co…
Reason
TreeHouse Foods is recalling products that may be impacted by sunflower seeds contaminated with Listeria monocytogenes.
Published
October 12, 2016
Distribution
US: AL, AZ, AR, CA, CO, CT, FL, IL, IN,…

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FDA Recall United States Terminated Historical recordClass I

Treehouse Foods

Product
UPC 071725728166, Natures Harvest Afternoon Snack Blend, Be…
Reason
TreeHouse Foods is recalling products that may be impacted by sunflower seeds contaminated with Listeria monocytogenes.
Published
October 12, 2016
Distribution
US: AL, AZ, AR, CA, CO, CT, FL, IL, IN,…

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FDA Recall United States Terminated Historical recordClass I

Treehouse Foods

Product
UPC 070038614142, Best Choice Mountain Trail Mix, Best By/…
Reason
TreeHouse Foods is recalling products that may be impacted by sunflower seeds contaminated with Listeria monocytogenes.
Published
October 12, 2016
Distribution
US: AL, AZ, AR, CA, CO, CT, FL, IL, IN,…

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FDA Recall United States Terminated Historical recordClass I

Treehouse Foods

Product
Sunflower Kernels packaged in the following brands and sizes…
Reason
TreeHouse Foods is recalling products that may be impacted by sunflower seeds contaminated with Listeria monocytogenes.
Published
October 12, 2016
Distribution
US: AL, AZ, AR, CA, CO, CT, FL, IL, IN,…

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FDA Recall Terminated Historical recordClass III

Lansoprazole Delayed-Release Capsules, USP, 30 mg, packaged in 100-count cartons of 10 x 10 unit dose blister cards, Rx only, Manufactured by: Dr. Reddy's Laboratories, Inc., 200 Somerset Corporate Blvd Floor 7, Bridgewater, NJ 08807, NDC 63739-0555-10

by Mckesson Packaging Services

Reason
Labeling: Label mix-up. The inner packaging was properly labeled Omeprazole DR 40mg Capsules, but the outer secondary packaging was mislabeled Lansoprazole Delayed-Release 30mg Capsules.
Published
October 5, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

PREMARIN (conjugated estrogen tablets, USP) 1.25 mg, 1000- count bottle, Rx only, Distributed by: Wyeth Pharmaceuticals Inc. A subsidiary of Pfizer Inc. Philadelphia, PA 19101, NDC 0046-1104-91

by Pfizer Inc.

Reason
Labeling: Incorrect or Missing Lot and/or Exp Date: Bottles were incorrectly labeled with an expiry date of 11/17; the correct date is 09/17.
Published
October 5, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Senna Syrup (sennosides) 8.8 mg, 8 fl. oz. (237 mL) bottle, Distributed by: Major Pharmaceuticals, 31778 Enterprise Drive, Livonia, MI 48150, NDC 0904-6289-09.

by Pharmatech LLC

Reason
CGMP Deviations: Recall initiated as a precautionary measure due to a potential risk of product contamination with the bacteria B. cepacia.
Published
October 5, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Senexon Liquid (sennosides) 8.8 mg, 8 fl oz. (237 mL) bottle, Distributed by: Rugby Laboratories, 31778 Enterprise Drive, Livonia, MI 48150, NDC 0536-1000-59.

by Pharmatech LLC

Reason
CGMP Deviations: Recall initiated as a precautionary measure due to a potential risk of product contamination with the bacteria B. cepacia.
Published
October 5, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Diocto Syrup (docusate sodium), 60 mg/15 mL, One Pint (473 mL) bottle, Dist. by: Rugby Laboratories, 31778 Enterprise Drive, Livonia, MI 48150, NDC 0536-1001-85.

by Pharmatech LLC

Reason
CGMP Deviations: Recall initiated as a precautionary measure due to a potential risk of product contamination with the bacteria B. cepacia.
Published
October 5, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Aller-Chlor (chlorpheniramine maleate) Syrup, USP, 2 mg in each 5 mL, 4 fl oz (120 mL) bottle, Distributed by: Rugby Laboratories, 31778 Enterprise Drive, Livonia, MI 48150, NDC 0536-1025-47.

by Pharmatech LLC

Reason
CGMP Deviations: Recall initiated as a precautionary measure due to a potential risk of product contamination with the bacteria B. cepacia.
Published
October 5, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Ninjacof-A (acetaminophen, chlophedianol HCl, pyrilamine maleate) Liquid, 160 mg/12.5 mg/12.5 mg in each 5 mL, 16 fl oz (473 mL) bottle, Manufactured for: Centurion Labs, LLC, Birmingham, AL 35243, NDC 23359-033-16.

by Pharmatech LLC

Reason
CGMP Deviations: Recall initiated as a precautionary measure due to a potential risk of product contamination with the bacteria B. cepacia.
Published
October 5, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Ninjacof (chlophedianol HCl and pyrilamine maleate) Liquid, 12.5 mg/12.5 mg in each 5 mL, 16 fl oz (473 mL) bottle, Manufactured for: Centurion Labs, LLC, Birmingham, AL 35243, NDC 23359-032-16.

by Pharmatech LLC

Reason
CGMP Deviations: Recall initiated as a precautionary measure due to a potential risk of product contamination with the bacteria B. cepacia.
Published
October 5, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Sennazon (sennosides) Syrup, 8.8 mg, 8 fl. oz. (237 mL) bottle, Mfd. for: Bayshore Pharmaceuticals, Tampla, FL 33619, NDC 76518-100-08.

by Pharmatech LLC

Reason
CGMP Deviations: Recall initiated as a precautionary measure due to a potential risk of product contamination with the bacteria B. cepacia.
Published
October 5, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Lamotrigine Tablets, USP, 150 mg, 500-count Tablets per bottle, Rx only, Manufactured by: Unichem Laboratories LTD., Pilerne Ind. Estate, Pilerne, Bardez, Goa 403 511 India; Marketed by: Unichem Pharmaceuticals (USA), Inc ., Rochelle Park, NJ 07662; NDC 29300-113-05.

by UNICHEM PHARMACEUTICALS USA INC

Reason
Tablets/Capsules Imprinted With Wrong ID: incorrect imprint debossed on the tablets.
Published
October 5, 2016
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Global Garlic, Inc.

Product
Ducal Apple Nectar, 5.3 oz cans.
Reason
Florida Department of Agriculture and Consumer Services surveillance sample tested positive for arsenic above 10 ppb.
Published
October 5, 2016
Distribution
FL, GA, IA, IL, NC, RI, TN, TX, VA, & WA…

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FDA Recall United States Terminated Historical recordClass I

Grassfields Cheese, LLC

Product
Crofters 12 pound wheels, Six pound half wheels, and wedges…
Reason
contamination with Shiga toxin-producing E. coli (STEC), a bacteria that can cause serious illness in humans. E.coli infection symptoms vary by individual, but often include severe stomach cramps, diarrhea (often bloody), and vomiting. If there is fever, it usually is not very high (less than 101¿F/less than 38.5¿C). Most people get better within 57 days. Some infections are very mild, but others are severe or even life-threatening. Around 510% of those diagnosed with Shiga-toxin producing E.coli infections develop a potentially life-threatening complication known as hemolytic uremic syndrome (HUS). Signs that a person is developing HUS include decreased frequency of urination, feeling very tired, and losing pink color in cheeks and inside the lower eyelids. Persons with HUS should be hospitalized because their kidneys may stop working and they may develop other serious problems. Most persons with HUS recover within a few weeks, but some suffer permanent damage or die.
Published
October 5, 2016
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

Grassfields Cheese, LLC

Product
Polkton Corners 12 pound wheels, Six pound half wheels, and…
Reason
contamination with Shiga toxin-producing E. coli (STEC), a bacteria that can cause serious illness in humans. E.coli infection symptoms vary by individual, but often include severe stomach cramps, diarrhea (often bloody), and vomiting. If there is fever, it usually is not very high (less than 101¿F/less than 38.5¿C). Most people get better within 57 days. Some infections are very mild, but others are severe or even life-threatening. Around 510% of those diagnosed with Shiga-toxin producing E.coli infections develop a potentially life-threatening complication known as hemolytic uremic syndrome (HUS). Signs that a person is developing HUS include decreased frequency of urination, feeling very tired, and losing pink color in cheeks and inside the lower eyelids. Persons with HUS should be hospitalized because their kidneys may stop working and they may develop other serious problems. Most persons with HUS recover within a few weeks, but some suffer permanent damage or die.
Published
October 5, 2016
Distribution
Multiple states

View recall →

FDA Recall United States Terminated Historical recordClass I

Grassfields Cheese, LLC

Product
Fait Fras 12 pound wheels, Six pound half wheels, and wedge…
Reason
contamination with Shiga toxin-producing E. coli (STEC), a bacteria that can cause serious illness in humans. E.coli infection symptoms vary by individual, but often include severe stomach cramps, diarrhea (often bloody), and vomiting. If there is fever, it usually is not very high (less than 101¿F/less than 38.5¿C). Most people get better within 57 days. Some infections are very mild, but others are severe or even life-threatening. Around 510% of those diagnosed with Shiga-toxin producing E.coli infections develop a potentially life-threatening complication known as hemolytic uremic syndrome (HUS). Signs that a person is developing HUS include decreased frequency of urination, feeling very tired, and losing pink color in cheeks and inside the lower eyelids. Persons with HUS should be hospitalized because their kidneys may stop working and they may develop other serious problems. Most persons with HUS recover within a few weeks, but some suffer permanent damage or die.
Published
October 5, 2016
Distribution
Multiple states

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.