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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
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 13,621–13,640 of 18,563 recalls

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 I

Top Taste, Inc

Product
Frozen cinnamon rolls packaged under the following labels:…
Reason
The ingredient statement on the product labels list egg as an ingredient but fails to list eggs in the "Contains" information.
Published
October 5, 2016
Distribution
Distribution was made to MN, ND, and NE.

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FDA Recall United States Terminated Historical recordClass I

Bounce Life Style HQ

Product
Bounce Energy Ball Cashew & Pecan Vitality Lift, each loose…
Reason
Bounce Energy Ball Cashew & Pecan Vitality Lift is recalled because it has the potential to be contaminated with Listeria monocytogenes. This product contains sunflower kernels that were recalled by supplier SunOpta.
Published
October 5, 2016
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Bounce Life Style HQ

Product
Australia -Cashew Cinnamon - Caf¿ Bounce, each bulk bag cont…
Reason
Cashew Cinnamon - Caf¿ Bounce is recalled because it has the potential to be contaminated with Listeria monocytogenes. This product contains sunflower kernels that were recalled by supplier SunOpta.
Published
October 5, 2016
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Bounce Life Style HQ

Product
US - Bounce Apple Cinnamon Protein Punch Energy Balls (old n…
Reason
Apple Cinnamon Protein Punch Energy Ball product is recalled because it has the potential to be contaminated with Listeria monocytogenes. This product contains sunflower kernels that were recalled by supplier SunOpta.
Published
October 5, 2016
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Faribault Foods, Inc

Product
No-Salt-Added Black Beans, 15 oz. (425 g), packaged under th…
Reason
Faribault Foods is recalling 15 oz.No-Salt-Added Black Beans due to potential presence of plastic and/or metal pieces.
Published
October 5, 2016
Distribution
Multiple states

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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.