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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.

37,118
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/gf-blends-recalls-truly-aip-all-purpose-flour-and-bread-mix-and-eat-gangster-flat-bread-pizza-mixPublished September 18, 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 II24,343
Class I9,793
Class III2,887
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,343
Class I9,793
Class III2,887
Not Yet Classified1

Showing 8,661–8,680 of 18,163 recalls

FDA Recall Terminated Historical recordClass II

CVS Health Children's Mucus Relief Chest Congestion Plus Cough Dextromethorphan HBr Cough Suppressant Guaifenesin Expectorant Mixed Berry Flavor 20 Singe-Use Vials Per Carton 0.17 fl. oz. (5 mL), Distributed by: CVS Pharmacy, Inc. One CVS Drive, Woonsocket, RI 02895, NDC 69842-260-01, UPC 050428597675

by Unipharma, Llc.

Reason
CGMP Deviations: Recall as a precautionary measure due to potential risk of product contamination with the bacteria B. cepacia.
Published
May 22, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

CVS Health Children's Pain & Fever Acetaminophen 160 mg/5 mL Pain reliever/Fever reducer Single-Use Vials Cherry Flavor 20 Single-Use Vials per carton 0.17 fl. oz. (5 mL), Distributed by: CVS Pharmacy, Inc. One CVS Drive, Woonsocket, RI 02895, NDC 69842-0258-01, UPC 050428601891

by Unipharma, Llc.

Reason
CGMP Deviations: Recall as a precautionary measure due to potential risk of product contamination with the bacteria B. cepacia.
Published
May 22, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

Titanium 4000, capsule, 4000 mg, 1 count blister card, 30 blister display boxt, distributed by Titanium 4000 UPC 86077000020

by D.B.P. Distribution

Reason
Marketed without an approved NDA/ANDA: undeclared sildenafil and tadalafil.
Published
May 22, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Relpax (eletriptan HBr) 40 mg, a) 12 tablets 2 cards x six 40 mg tablets per blister pack, NDC 0049-2340-05; b) 6 tablets 1 card x six 40 mg tablets per blister pack, NDC 0049-2340-45, Rx Only, Made in Ireland, Distributed by Roerig, Division of Pfizer Inc, NY NY 10017.

by Pfizer Inc.

Reason
Labeling: Label Error on Declared Strength: an artwork error on the secondary packaging of Relpax 40 mg Tablets, indicates that each tablet contains eletriptan hydrobromide equivalent to 20mg eletriptan, instead of 40mg, on one side of the carton.
Published
May 22, 2019
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

AmeriHerb International Inc

Product
Goldenseal herb c/s, Hydrastis Canadensis, Not for use durin…
Reason
Dried spice and herb products potentially contaminated with generic E. coli.
Published
May 22, 2019
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

AmeriHerb International Inc

Product
Lemon balm leaf c/s, Melissa officinalis, 1# Net, AmeriHerb…
Reason
Dried spice and herb products potentially contaminated with generic E. coli.
Published
May 22, 2019
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

AmeriHerb International Inc

Product
Mullein leaf c/s, Verbascum Thapsus, 1# Net, AmeriHerb LLC,…
Reason
Dried spice and herb products potentially contaminated with generic E. coli.
Published
May 22, 2019
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

AmeriHerb International Inc

Product
Dill weed c/s, Anethum graveolens, 1# Net, AmeriHerb LLC, Am…
Reason
Dried spice and herb products potentially contaminated with generic E. coli.
Published
May 22, 2019
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

AmeriHerb International Inc

Product
Blessed thistle herb c/s, Centaurea benedicus, Not for use d…
Reason
Dried spice and herb products potentially contaminated with generic E. coli.
Published
May 22, 2019
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

AmeriHerb International Inc

Product
Parsley flakes, Petroselinum sativum, 1# Net, AmeriHerb LLC,…
Reason
Dried spice and herb products potentially contaminated with generic E. coli.
Published
May 22, 2019
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass III

Barlean's Llc

Product
Item FG 10079, Barleans, Flax Oil, 100 Softgels per bottle.…
Reason
Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.
Published
May 22, 2019
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass III

Barlean's Llc

Product
Item FG 10191, Barlean s Ideal CBD Hemp Oil Softgel, 900 mg…
Reason
Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.
Published
May 22, 2019
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass III

Barlean's Llc

Product
Item FG 10190, Barleans Full Spectrum Hemp Extract, 60 Softg…
Reason
Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.
Published
May 22, 2019
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass III

Barlean's Llc

Product
Item FG 10149, Barlean s, Omega Man, 120 Softgels per bottle…
Reason
Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.
Published
May 22, 2019
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass III

Barlean's Llc

Product
Item FG 10146, Barlean s, Essential Woman, 120 count Softgel…
Reason
Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.
Published
May 22, 2019
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass III

Barlean's Llc

Product
Item FG 10116, Barlean s, Master Blend Total Omega 3.6.9 Lem…
Reason
Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.
Published
May 22, 2019
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass III

Barlean's Llc

Product
Item FG 10106, Barlean s, Olive Leaf Complex, 120 Softgels p…
Reason
Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.
Published
May 22, 2019
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass III

Barlean's Llc

Product
Item FG 10089, Barlean s, Fish Oil Omega-3 EPA/DHA Orange F…
Reason
Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.
Published
May 22, 2019
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass III

Barlean's Llc

Product
Item FG 10085, Barleans, Ultra EPA-DHA Fish Oil 1,300 mg Ome…
Reason
Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.
Published
May 22, 2019
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass III

Barlean's Llc

Product
Item FG 10084, Barlean s, Ultra EPA Fish Oil 1250 mg Omega-3…
Reason
Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.
Published
May 22, 2019
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.