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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.

37,204
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
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 15,761–15,780 of 20,558 recalls

FDA Recall United States Terminated Historical recordClass I

Let's Do Lunch, Inc.

Product
Cafe Favorites Oven Roasted Turkey Breast & Cheese Melt on…
Reason
Potential Listeria monocytogenes contamination.
Published
August 17, 2016
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

Let's Do Lunch, Inc.

Product
Cafe Favorites Oven Roasted Turkey Breast & Cheese Deli Fla…
Reason
Potential Listeria monocytogenes contamination.
Published
August 17, 2016
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

Let's Do Lunch, Inc.

Product
Integrated Food Service Turkey Breast & Cheese Sandwich on…
Reason
Potential Listeria monocytogenes contamination.
Published
August 17, 2016
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Betamethasone Acetate / Betamethasone Sodium Phosphate Injectable Suspension, 7 mg/ mL,10 mL Multi-Dose vial for injection, Rx Only, Isomeric Pharmacy Solution, 2401 Foothill Dr., Salt Lake City, UT 84109

by Isomeric Pharmacy Solution, LLC

Reason
Lack of processing controls: Isomeric Pharmacy Solution, LLC is recalling Betamethasone Acetate / Betamethasone Sodium Phosphate 7 mg/mL INJ SUSP because of the potential of drug clumps in the vial of the sterile drug product and larger particle sizes.
Published
August 10, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Children's Qnasl 40 mcg (beclomethasone dipropionate) Nasal Aerosol, 40 mcg per spray, 60 Metered Sprays per canister, 4.9g Net Contents, Rx only; Professional Sample; Manufactured for Teva Respiratory, LLC, Horsham, PA 19044; By: 3M Drug Delivery Systems, Northridge, CA 91324; NDC 59310-206-08.

by Teva North America

Reason
Failed Content Uniformity Specifications: out of specification test result for spray content uniformity.
Published
August 10, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Oxygen Nasal Wash (purified water, xylitol, stabilized oxygen, sodium chloride) solution, .75 oz (22mL) bottle, Distributed by: Let's Talk Health, Chula Vista, CA 91914.

by Let's Talk Health, Inc.

Reason
Marketed Without An Approved NDA/ANDA: product is an unapproved drug due to nasal decongestant claims as well as not complying with the nasal decongestant final monograph.
Published
August 10, 2016
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Creative Snacks Co., LLC

Product
Creative Snacks Brain Food, 3.5 oz. Snack Bag, UPC 816512015…
Reason
Potential presence of Listeria Monocytogenes
Published
August 10, 2016
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

Creative Snacks Co., LLC

Product
Creative Snacks Co. Roasted, Salted Sunflower Seeds, 10 lb.…
Reason
Potential presence of Listeria Monocytogenes
Published
August 10, 2016
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass II

S-L Snacks NC, LLC

Product
Lance Oyster Crackers, Dist. by Snyder's-Lance, Inc., Charlo…
Reason
May contain low levels of peanut residue.
Published
August 10, 2016
Distribution
AL, FL, GA, IL, IN, IA, KS, KY, LA, MD,…

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FDA Recall United States Terminated Historical recordClass I

Inner Health Group, Inc dba Michael's Naturopathic Programs

Product
Michael's Naturopathic Programs Cholesterol Metabolism Facto…
Reason
May contain undeclared milk (in the form of calcium caseinate) and soy.
Published
August 10, 2016
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

The Kroger Co

Product
Kroger DELUXE ICE CREAM S'MORES 48 FL OZ (1.5 QT) 1.4 ML ING…
Reason
The firm was notified that the product was manufactured with an ingredient that may contain low levels of peanut reside which is not declared in the ingredient statement.
Published
August 10, 2016
Distribution
Product was shipped to the following sta…

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FDA Recall United States Terminated Historical recordClass I

Ach Food Companies Inc

Product
Salad topping labeled under the following brand names: (Pr…
Reason
Product manufactured with ingredient which may be contaminated with Listeria monocytogenes.
Published
August 10, 2016
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Honey Bunchie, LLC

Product
Honey Bunchies Gourmet Honey Bars, 1.9 oz. snack bar contain…
Reason
Honey Bunchie, LLC is initiating a voluntary recall of a limited number of Honey Bunchies Gourmet Honey Bars that contain SunOpta sunflower kernels that have the potential of contamination with Listeria monocytogenes.
Published
August 10, 2016
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Club Chef LLC

Product
Diced and sliced yellow onions. 2.5 lb & 5 lb clear plastic…
Reason
The firm was notified by a customer that the whole uncut product test positive for Listeria
Published
August 10, 2016
Distribution
Product was shipped to the following sta…

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FDA Recall United States Terminated Historical recordClass I

Creative Snacks Co., LLC

Product
Creative Snacks Co. Roasted, No Salt Sunflower Seeds, 9 oz.…
Reason
Potential presence of Listeria Monocytogenes
Published
August 10, 2016
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

Creative Snacks Co., LLC

Product
Creative Snacks Co. Sunny Day Splendor, 10 lb. bulk, UPC 816…
Reason
Potential presence of Listeria Monocytogenes
Published
August 10, 2016
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

Creative Snacks Co., LLC

Product
Fresh Market Healthy Snackin, 25 lb. bulk, UPC n/a
Reason
Potential presence of Listeria Monocytogenes
Published
August 10, 2016
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

Creative Snacks Co., LLC

Product
Creative Snacks Co. Hold the Salt!, 10 lb. bulk, UPC 8165120…
Reason
Potential presence of Listeria Monocytogenes
Published
August 10, 2016
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

Creative Snacks Co., LLC

Product
Plentiful Planet Heart Smart Mix, 25 lb. bulk, UPC 030684710…
Reason
Potential presence of Listeria Monocytogenes
Published
August 10, 2016
Distribution
Multiple states

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FDA Recall Terminated Historical recordClass III

mitoXANTRONE Injection USP (concentrate), 20 mg/10 mL (2 mg/mL), 10 mL Multiple Dose Vial packaged in a carton, Rx only, Teva Parenteral Medicines, Inc., Irvine, CA 92618, NDC 0703-4685-01.

by Teva North America

Reason
Failed Impurities/Degradation Specifications: High out of specification results for Impurity D.
Published
August 3, 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.