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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.

36,949
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,732
Class I recallsReasonable probability of serious health consequences
24,263
Class II recallsTemporary or medically reversible health consequences
2,873
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 2,071 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)

  • 1,458 recalls have been announced year to date.
  • Aug 2026 was 53% 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 II24,263
Class I9,732
Class III2,873
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,263
Class I9,732
Class III2,873
Not Yet Classified1

Showing 1–20 of 36,949 recalls

FDA Recall United States Status not reported 2026 record

Foods Alive Recalls Organic Moringa Leaf Powder Because of Possible Health Risk

Reason
Foods Alive Inc of Angola, IN, is recalling its 8-ounce packages of organic moringa leaf powder because they have the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened
Published
September 4, 2026

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FDA Recall United States Status not reported 2026 record

SUPPLX.com Issues Voluntary Nationwide Recall of Business Pill and Branch Manager for Men Due to Undeclared Yohimbine

Reason
Grant-Valkaria, Florida - SUPPLX.com is voluntarily recalling Business Pill and Branch Manager for Men, products marketed as dietary supplements for male sexual enhancement, because FDA laboratory analysis confirmed that both products contain yohimbine that is not declared on the product labels.
Published
September 3, 2026

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FDA Recall United States Status not reported 2026 record

American Regent, Inc. Issues Voluntary Nationwide Recall of Three Lots of Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) Due to the Presence of Particulate Matter and Lack of Assurance of Sterility

Reason
FOR IMMEDIATE RELEASE – September 3, 2026 – New Albany, OH, American Regent, Inc. is conducting a nationwide voluntary recall of three lots of Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) multi dose vials to the consumer level. Customer complaints were received for leaking and cracked vials, re
Published
September 3, 2026

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FDA Recall United States Status not reported 2026 record

Frutas y Hortalizas del Sur S.A. Expands Recall to Include One Lot of Great Value Frozen Organic Triple Berry Blend Because of Potential Contamination with Escherichia coli O145:H28 (E. coli O145)

Reason
September 02, 2026. Frutas y Hortalizas del Sur S.A., San Carlos, Chile expands its July 3, 2026, recall of frozen organic IQF blueberries to include one lot of Great Value frozen Organic Triple Berry Blend 10 OZ because of potential contamination with Escherichia coli O145:H28 (E. coli O145).
Published
September 2, 2026

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FDA Recall United States Status not reported 2026 record

Crystal Temptations Issues Allergy Alert on Undeclared Milk in Chocolatey Eyeballs

Reason
Crystal Temptations of North Arlington, NJ is recalling Halloween Chocolatey Eyeballs because they contain undeclared MILK allergens. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume these products.
Published
August 31, 2026

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FDA Recall United States Status not reported 2026 record

LMSI LLC/Kofinas Olive Oil Issues a Voluntary Recall of its Garlic Mediterranean Infused Extra Virgin Olive Oil for Using a Garlic Essential Oil Not Approved for Culinary Use

Reason
Cincinnati, OH (Aug. 29, 2026) - LMSI LLC/ Kofinas Olive Oil is issuing a voluntary recall of its Garlic Mediterranean infused extra virgin olive oil for using a garlic essential oil not approved for culinary use. The flavored oil was bottled in glass bottles in 500 ml, 250 ml, and 100 ml sizes.
Published
August 31, 2026

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FDA Recall United States Status not reported 2026 record

Northwest Naturals Voluntarily Recalls Two Raw Pet Food Products Because of Possible Salmonella & Listeria Monocytogenes Health Risk

Reason
Northwest Naturals of Portland, Oregon is voluntarily recalling 53 cases (1,272 lbs.) of Northwest Naturals Frozen Chicken Recipe (cat food 2 lbs. bag) and 19 cases (684 lbs.) of Northwest Naturals Frozen Raw Diet for Dogs Chicken Recipe (6 lbs. bag) in the two lots identified due to Salmonella and
Published
August 29, 2026

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FDA Recall United States Status not reported 2026 record

Everything Sprouts, LLC Expands Voluntarily Recall to Include Robust Radish Mix Due to Potential E. Coli and Salmonella Risk

Reason
Everything Sprouts, LLC, based in Minneapolis, MN is expanding its voluntary recall of sprouts to include certain lots of Robust Radish Sprout Mix because it has the potential to be contaminated with Shiga toxin producing Escherichia coli (STEC) or Salmonella bacteria.
Published
August 28, 2026

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FDA Recall United States Status not reported 2026 record

Panorama Produce Recalls Mangoes Due to Possible Salmonella Contamination

Reason
MAMARONECK, NY, AUG. 28, 2026 - Panorama Produce is recalling 302 boxes of size 9 (nine) mangoes because they may be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. H
Published
August 28, 2026

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USDA FSIS Recall United States Status not reported 2026 record

Shanghai Ravioli Corporation Recalls Not Ready-To-Eat Frozen Buffalo Chicken Products Produced Without the Benefit of Inspection

Reason
<img align="left" hspace="5" src="https://www.fsis.usda.gov/sites/default/files/2023-04/Icon-Recalls.png"/> WASHINGTON, Aug. 26, 2026 - Shanghai Ravioli Corporation, in Boston, Mass., is recalling approximately 24,900 pounds of frozen, not ready-to-eat (NRTE) Buffalo chicken products that were produced without the benefit...
Published
August 26, 2026

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FDA Recall United States Status not reported 2026 record

Revival Animal Health, LLC Voluntarily Recalls Feline Milk Replacers Due to Inconsistent Levels of Vitamins and Trace Minerals

Reason
Revival Animal Health of Orange City, IA is recalling Breeder’s Edge® and Shelter’s Choice® Feline Milk Replacers due to low, levels of potassium, copper, folic acid, choline and/or pyridoxine (vitamin B6).
Published
August 26, 2026

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FDA Recall United States Status not reported 2026 record

Jaime’s Foods ATX Issues Allergy Alert on Undeclared Egg Allergen in Jaime’s Spanish Village Jalapeno Ranch

Reason
Jaime’s Foods ATX of Austin, TEXAS is recalling Jaime’s Spanish Village Jalapeno Ranch because it contains undeclared eggs. People who have an allergy or severe sensitivity to eggs run the risk of serious or life-threatening allergic reaction if they consume this product.
Published
August 25, 2026

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FDA Recall United States Status not reported 2026 record

The Better Bakehouse Snack Company is Recalling Certain Lots of Donutful Chocolate Dipped Vanilla Cake Donuts to Undeclared Milk Allergen

Reason
Las Vegas, NV – August 24, 2026 – The Better Bakehouse Snack Company is recalling certain lots of Donutful Chocolate Dipped Vanilla Cake Donuts because the product may contain undeclared milk. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening aller
Published
August 25, 2026

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FDA Recall United States Status not reported 2026 record

Everything Sprouts, LLC Recalls Alfalfa Sprouts Due to Potential E. Coli and Salmonella Risk

Reason
Everything Sprouts, LLC, based in Minneapolis, MN is recalling certain lots of Alfalfa Sprouts because it has the potential to be contaminated with Shiga toxin producing Escherichia coli (STEC) or Salmonella bacteria.Shiga toxin-producing Escherichia coli (STEC) are organisms that can cause serious
Published
August 22, 2026

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FDA Recall Ongoing 2026 recordClass I

Optiray Imaging Bulk Package-350, Ioversol Injection 74%, 350 mg/mL Organically Bound Iodine, 500 mL Multiple-Dose Vial, Rx only, Sterile Solution, Manufactured by: Liebel-Flarsheim Company LLC, Raleigh, NC 27616, Made in USA, NDC 0019-1333-65.

by Liebel-Flarsheim Company LLC

Reason
Presence of Particulate Matter: comprising polyethylene and other plastic materials, stainless steel and glass.
Published
August 19, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass I

Glutathione (MDV), 200 mg/mL, 30 mL vial, each mL contains Glutathione 200 mg, Ascorbic Acid 20 mg, Benzyl Alcohol 1.5%, Na Hydroxide (Ph Adjust) in sterile water for injection, VMC.

by Victory Medical Center Pharmacy

Reason
Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin.
Published
August 19, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass I

Kian Pee Wan Capsules, 30-count bottles

by Buy-Herbal

Reason
Marketed Without an Approved NDA/ANDA: Product contains undeclared drug ingredients dexamethasone and cyproheptadine.
Published
August 19, 2026
Distribution
Product was sold to individual consumers…

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FDA Recall Ongoing 2026 recordClass II

CLINDAMYCIN PALMITATE HYDROCHLORIDE FOR ORAL SOLUTION, USP, 75 mg/5 mL, Rx Only, 100 mL, Distributed by: Avet Pharmaceuticals Inc., East Brunswick, NJ 08816, NDC 23155-603-51

by Heritage Pharmaceuticals Inc

Reason
Presence of Foreign Substance: presence of particles and white flakes in the reconstituted bottles.
Published
August 19, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

CLEAR EYES Maximum Itchy Eye Relief, 0.5 fl oz (15 mL) per dropper bottle, Sterile, Dist. by Medtech Products Inc., Tarrytown, NY 10591, a Prestige Consumer Healthcare Company. NDC: 67172-999-01 UPC 6 78112 65920 3

by Prestige Brands Holdings

Reason
Lack of assurance of sterility. The recall is due to potential contamination
Published
August 19, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

SILDENAFIL CITRATE USP, 1.00KG, 1.00KG-bag Net Wt. Rx only " For Prescription Compounding Only", Shoolin Pharma Chem LLP, Block/Survey no 408, B/H Ratnamani Tubes, Near Maruti Inox, Indrad, Kadi, Mahesania, Gujarat, 382715, India, (CAS NO. 171599-83-0) NDC 85702-001-08.

by Shoolin Pharma Chem LLP

Reason
CGMP Deviations:Noted during FDA inspection
Published
August 19, 2026
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.