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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 November 2026.

37,449
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,872
Class I recallsReasonable probability of serious health consequences
24,509
Class II recallsTemporary or medically reversible health consequences
2,932
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 2,096 recalls
Newest recallhttps://www.fsis.usda.gov/recalls-alerts/fsis-issues-public-health-alert-meat-and-poultry-products-due-misbranding-andPublished November 6, 2026
Most affected stateHawaii 200 recalls mention this state

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Download matching recalls as CSV

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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)

  • 1,956 recalls have been announced year to date.
  • Oct 2026 was 4% higher than the previous complete period (Sep 2026: 209).
  • The highest complete period was Jun 2026 (300).
  • Nov 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 II24,509
Class I9,872
Class III2,932
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,509
Class I9,872
Class III2,932
Not Yet Classified2

Showing 9,101–9,120 of 18,373 recalls

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

View recall →

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

View recall →

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

View recall →

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

View recall →

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

View recall →

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

View recall →

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

View recall →

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

View recall →

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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FDA Recall United States TerminatedTerminated: March 13, 2020Historical recordClass II

Back Roads Food Company

Product
Back Roads Granola: Maple Spice Best by date: 01/11/20-02/2…
Reason
Products may contain pieces of aluminum.
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: Maple Pecan Best by date: 01/11/20-02/…
Reason
Products may contain pieces of aluminum.
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: Coconut Ginger Best by date: 01/11/20-…
Reason
Products may contain pieces of aluminum.
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: Coconut Crunch Best by date: 01/11/…
Reason
Products may contain pieces of aluminum.
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: Original Best by date: 01/11/20-02/2…
Reason
Products may contain pieces of aluminum.
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: Gluten Free Best by date: 01/11/20-02/…
Reason
Products may contain pieces of aluminum.
Published
May 22, 2019
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: March 13, 2020Historical recordClass II

Back Roads Food Company

Product
Back Roads Granola: Dark Chocolate Pecan Best by date: 01/1…
Reason
Products may contain pieces of aluminum.
Published
May 22, 2019
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: March 13, 2020Historical recordClass II

Back Roads Food Company

Product
Back Roads Granola: Ancient Grains Best by date: 01/11/20-0…
Reason
Products may contain pieces of aluminum.
Published
May 22, 2019
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: June 20, 2023Historical recordClass I

Mycophenolate Mofetil for Injection, USP 500 mg, 4 Single Dose Vials, Rx Only, Distributed by: Par Pharmaceutical Chestnut Ridge, NY 10977 NDC 342023-172-044

by Par Pharmaceutical, Inc.

Reason
Presence of Particulate Matter; glass fragment observed in one vial of reconstituted product
Published
May 15, 2019
Distribution
Nationwide

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FDA Recall TerminatedTerminated: August 14, 2019Historical recordClass I

FENTANYL Transdermal System, 12 mcg/h, five (12 mcg/h) systems per carton, Rx only, Distributed by: Alvogen, Inc., Pine Brook, NJ 07058; Manufactured by: 3M Drug Delivery Systems, St. Paul, MN 55107, NDC 47781-423-47.

by Alvogen, Inc

Reason
Product Mix-Up: Customer complaint that their carton labeled as Fentanyl Transdermal Systems, 12 mcg/h contained five patches labeled and containing 50 mcg/h.
Published
May 15, 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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