Skip to main content
Get Alerts

Data Explorer

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.

37,116
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/saratoga-potato-chips-issues-allergy-alert-undeclared-soy-j-higgs-loaded-bacon-and-cheddar-potatoPublished September 16, 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.

Filters
Recall details
Location
Date range
Sort results
Clear filters
Metric
View
Recalls announced by month (Year to date)

A chart of recalls grouped by month.

Download CSV

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 8,601–8,620 of 18,020 recalls

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 →

FDA Recall United States Terminated Historical 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 Terminated Historical 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

View recall →

FDA Recall United States Terminated Historical 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

View recall →

FDA Recall United States Terminated Historical 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

View recall →

FDA Recall United States Terminated Historical 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

View recall →

FDA Recall United States Terminated Historical 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

View recall →

FDA Recall United States Terminated Historical 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

View recall →

FDA Recall United States Terminated Historical 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

View recall →

FDA Recall United States Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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

View recall →

FDA Recall Terminated Historical 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

View recall →

FDA Recall Terminated Historical recordClass II

Ketorolac Tromethamine Injection, USP, 60 mg per 2 mL (30 mg per mL), 2 mL Vials, Rx only, Mfd. for Sagent Pharmaceuticals, Schaumburg, IL 60195, NDC: 25021-701-02

by Sagent Pharmaceuticals Inc

Reason
Lack of Sterility Assurance: Microbial growth detected during a routine simulation of the manufacturing process, which represents the potential introduction of microorganisms into the products.
Published
May 15, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Carvedilol Tablets, USP, 6.25 mg, 500 count bottles, Rx Only Manufactured by: Cadila Healthcare Ltd., India Distributed by: Zydus Pharmaceuticals (USA) Inc. Pennington, NJ USA 08534 NDC 68382-093-05

by Zydus Pharmaceuticals USA Inc

Reason
Labeling; Label Mix-up; report received of one bottle labeled as Acyclovir Tablets USP 400 mg actually contained Carvedilol Tablets 6.25 mg
Published
May 15, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Acyclovir Tablets, USP, 400 mg, 100 count bottles, Rx Only Manufactured by: Cadila Healthcare Ltd., India Distributed by: Zydus Pharmaceuticals (USA) Inc. Pennington, NJ USA 08534 NDC 68382-791-01

by Zydus Pharmaceuticals USA Inc

Reason
Labeling; Label Mix-up; report received of one bottle labeled as Acyclovir Tablets USP 400 mg actually contained Carvedilol Tablets 6.25 mg
Published
May 15, 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.