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Recall totals

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

37,341
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,860
Class I recallsReasonable probability of serious health consequences
24,450
Class II recallsTemporary or medically reversible health consequences
2,901
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 2,095 recalls
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/haifa-smoked-fish-recalls-cold-smoked-sprats-due-potential-health-riskPublished October 27, 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)

  • 1,739 recalls have been announced year to date.
  • Sep 2026 was 15% higher than the previous complete period (Aug 2026: 182).
  • The highest complete period was Jun 2026 (300).
  • Oct 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 II24,450
Class I9,860
Class III2,901
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,450
Class I9,860
Class III2,901
Not Yet Classified2

Showing 8,241–8,260 of 17,454 recalls

FDA Recall TerminatedTerminated: April 26, 2021Historical 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 TerminatedTerminated: June 12, 2019Historical 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 TerminatedTerminated: June 12, 2019Historical 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 TerminatedTerminated: June 12, 2019Historical 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 TerminatedTerminated: June 12, 2019Historical 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

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FDA Recall United States TerminatedTerminated: June 12, 2019Historical 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

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FDA Recall United States TerminatedTerminated: June 12, 2019Historical 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

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FDA Recall United States TerminatedTerminated: October 15, 2020Historical 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 TerminatedTerminated: October 15, 2020Historical 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 TerminatedTerminated: October 15, 2020Historical 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

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FDA Recall United States TerminatedTerminated: October 15, 2020Historical 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

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FDA Recall United States TerminatedTerminated: October 15, 2020Historical 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

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FDA Recall United States TerminatedTerminated: October 15, 2020Historical 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

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FDA Recall United States TerminatedTerminated: October 15, 2020Historical 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

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FDA Recall United States TerminatedTerminated: October 15, 2020Historical 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

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FDA Recall United States TerminatedTerminated: October 15, 2020Historical 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

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FDA Recall United States TerminatedTerminated: October 15, 2020Historical 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

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FDA Recall United States TerminatedTerminated: October 15, 2020Historical recordClass III

Barlean's Llc

Product
Item FG 10083, Barlean's, Ultra DHA Fish Oil Omega-3, Lemona…
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 TerminatedTerminated: October 15, 2020Historical recordClass III

Barlean's Llc

Product
Item FG 10037, Barlean s Cod Liver Oil Omega 3 EPA/DHA with…
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 TerminatedTerminated: March 13, 2020Historical recordClass II

Back Roads Food Company

Product
Back Roads Granola: Nut Free Best by date: 01/11/20-02/2/20…
Reason
Products may contain pieces of aluminum.
Published
May 22, 2019
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.

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