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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 October 2026.

37,205
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,841
Class I recallsReasonable probability of serious health consequences
24,366
Class II recallsTemporary or medically reversible health consequences
2,892
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 2,073 recalls
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/gias-foods-inc-recalls-bettergoods-authentic-italian-lemon-alfredo-fettuccine-because-possible-0Published October 1, 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)

  • 1,714 recalls have been announced year to date.
  • Sep 2026 was 3% higher than the previous complete period (Aug 2026: 182).
  • The highest complete period was Jun 2026 (297).
  • 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 II24,366
Class I9,841
Class III2,892
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,366
Class I9,841
Class III2,892
Not Yet Classified2

Showing 14,901–14,920 of 20,441 recalls

FDA Recall United States Terminated Historical recordClass I

Troyer Cheese Inc

Product
BACKROAD COUNTRY PEANUT BUTTER PRETZELS, Net Wt. 7 oz (198g)…
Reason
The product has been recalled because it has the potential to be contaminated with Listeria monocytogenes.
Published
December 21, 2016
Distribution
Prodeuct was shipped to the following st…

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FDA Recall United States Terminated Historical recordClass I

Troyer Cheese Inc

Product
BACKROAD COUNTRY HONEY ISLAND CRUNCH MIX ,Net Wt. 9 oz (256g…
Reason
The product has been recalled because it has the potential to be contaminated with Listeria monocytogenes.
Published
December 21, 2016
Distribution
Prodeuct was shipped to the following st…

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FDA Recall United States Terminated Historical recordClass I

Back To Nature Foods, Llc

Product
Back to Nature Mini Chocolate Chunk Cookies, 6 - 1.25oz (35g…
Reason
Produces contains undeclared milk.
Published
December 21, 2016
Distribution
Products distributed to the following st…

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FDA Recall United States Terminated Historical recordClass I

Back To Nature Foods, Llc

Product
Back to Nature Chocolate Chunk Cookies, 9.5 oz (269g) . pouc…
Reason
Produces contains undeclared milk.
Published
December 21, 2016
Distribution
Products distributed to the following st…

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FDA Recall United States Terminated Historical recordClass I

Back To Nature Foods, Llc

Product
Back to Nature, Gluten Free, Dark Chocolate Coconut Granola,…
Reason
Produces contains undeclared milk.
Published
December 21, 2016
Distribution
Products distributed to the following st…

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FDA Recall United States Terminated Historical recordClass I

Back To Nature Foods, Llc

Product
Back to Nature, Gluten-Free, Chocolate Delight Granola, 11 o…
Reason
Produces contains undeclared milk.
Published
December 21, 2016
Distribution
Products distributed to the following st…

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FDA Recall United States Terminated Historical recordClass I

American Blue Ribbon Holdings DBA Legendary Baking

Product
Ultimate Chocolate Chip Cookie Dough Pie, refrigerated/froze…
Reason
Product incorporated cookie dough that was potentially contaminated with Listeria Monocytogenes.
Published
December 21, 2016
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass II

Waymouth Farms, Inc

Product
Good Sense Trail Mix, Cranberries 'N More, Net Wt. 6 oz. (17…
Reason
Good Sense Cranberries 'N More, 6 oz., may contain undeclared pecans, walnuts, wheat, milk and soy.
Published
December 21, 2016
Distribution
AR, IA, IL, KS, LA, MN, MO, ND, NE, NY,…

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FDA Recall United States Terminated Historical recordClass I

Troyer Cheese Inc

Product
BACKROAD COUNTRY CRANBERRY NUT DELIGHT MIX, Net Wt. 9 oz (25…
Reason
The product has been recalled because it has the potential to be contaminated with Listeria monocytogenes.
Published
December 21, 2016
Distribution
Prodeuct was shipped to the following st…

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FDA Recall Terminated Historical recordClass II

USCG Boat Response Kit - Product Code 80-0353, North American Rescue

by North American Rescue LLC.

Reason
Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
Published
December 14, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Aid Backpack Kit - Product Code 85-0917, North American Rescue

by North American Rescue LLC.

Reason
Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
Published
December 14, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Mini Resupply Trauma Kit - Product Code 85-0835, North American Rescue

by North American Rescue LLC.

Reason
Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
Published
December 14, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Amphibious Trauma Kit - Product Code 85-0639, North American Rescue

by North American Rescue LLC.

Reason
Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
Published
December 14, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

K-9 Trauma Field Kit - Product Code 80-0211, 80-0304, 80-0209, 80-0210, 80-0300, 80-0301, North American Rescue

by North American Rescue LLC.

Reason
Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
Published
December 14, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Advance Trauma Kit - Product Code 85-0742, 85-0746, 85-0745, 85-0639, 85-0744, 85-0744, 85-0741, North American Rescue

by North American Rescue LLC.

Reason
Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
Published
December 14, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Range Trauma Kit - Product Code 85-1274, North American Rescue

by North American Rescue LLC.

Reason
Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
Published
December 14, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Range Trauma Kit ORG - Product Code 80-0213, 80-0299, 80-0298, North American Rescue

by North American Rescue LLC.

Reason
Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
Published
December 14, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Range Trauma Kit Hardcase - Product Code 85-0889, North American Rescue

by North American Rescue LLC.

Reason
Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
Published
December 14, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

SODIUM FERRIC GLUCONATE COMPLEX IN SUCROSE INJECTION, 62.5mg elemental iron/5mL, 10 (5mL vials) per shelf pack, Rx only, Mfd: Hikma Farmaceutica (Portugal,) SA Distributed by: Westward Eatowntown NJ 07724 USA, Shelf pack NDC 0143-9570-10, Unit dose NDC 0143-9570-01

by West-Ward Pharmaceuticals Corp.

Reason
Subpotent Drug: Product has an an out of specification in iron assay analysis found during 18 month stability testing.
Published
December 14, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Qnasl (beclomethasone dipropionate) Nasal Aerosol 80 Mcg, 50 Metered Sprays, Rx only, Manufactured for Teva Respiratory, LLC, Horsham, PA 19044, By: 3M Drug Delivery Systems, Northridge, CA 91324, NDC 59310-210-13.

by Teva Pharmaceuticals USA

Reason
Failed Content Uniformity: Product was out of specification for spray content uniformity obtained during stability testing.
Published
December 14, 2016
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.