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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.

37,139
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,799
Class I recallsReasonable probability of serious health consequences
24,349
Class II recallsTemporary or medically reversible health consequences
2,891
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
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)

  • 1,527 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 II24,349
Class I9,799
Class III2,891
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,349
Class I9,799
Class III2,891
Not Yet Classified1

Showing 12,041–12,060 of 20,954 recalls

FDA Recall United States Terminated Historical recordClass I

The King Arthur Flour Company, Inc.

Product
King Arthur Flour, 100% Organic, Finely Ground, Coconut Flou…
Reason
Coconut flour tested positive for Salmonella.
Published
April 11, 2018
Distribution
Multiple states

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FDA Recall Terminated Historical recordClass III

24-HOUR Oral Care q4 Kit with Ballard* Technology, containing 2 Toothbrush Packs with CHG Solution, Chlorhexidine Gluconate Oral Rinse, 0.12%, 15 mL unit dose cup (NDC 50383-720-15), Rx Only, Hi-Tech Pharmacal Co., Inc. Amityville, NY 11701; Kit Manufactured by Halyard Health, Inc., 5405 Windward Parkway, Alpharetta, GA 30004; Distributed in the USA by Halyard Sales, LLC, Alpharetta, GA 30004, Product 97014.

by Akorn, Inc.

Reason
Subpotent Drug: Product crystallization with accompanying low out of specification results for chlorhexidine assay.
Published
April 4, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

24-HOUR Oral Care q2 Kit with Ballard* Technology, containing 2 Toothbrush Packs with CHG Solution, Chlorhexidine Gluconate Oral Rinse, 0.12%, 15 mL unit dose cup (NDC 50383-720-15), Rx Only, Hi-Tech Pharmacal Co., Inc. Amityville, NY 11701; Kit Manufactured by Halyard Health, Inc., 5405 Windward Parkway, Alpharetta, GA 30004; Distributed in the USA by Halyard Sales, LLC, Alpharetta, GA 30004, Product 97012.

by Akorn, Inc.

Reason
Subpotent Drug: Product crystallization with accompanying low out of specification results for chlorhexidine assay.
Published
April 4, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Chlorhexidine Gluconate Oral Rinse, 0.12%, 15 mL unit dose cups (NDC 50383-720-15) packaged in 100-count (10 x 10) cups per case pack (NDC 50383-720-18 or 50383-720-19), Rx Only, Hi-Tech Pharmacal Co., Inc., Amityville, NY 11701.

by Akorn, Inc.

Reason
Subpotent Drug: Product crystallization with accompanying low out of specification results for chlorhexidine assay.
Published
April 4, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Fosphenytoin Sodium Injection, USP 500 mg PE*/10 mL, Made in India. Distributed by: Amneal Biosciences, Bridgewater, NJ 08807, NDC 70121-1390-1

by Amneal Pharmaceuticals

Reason
Presence of particulate matter
Published
April 4, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Evamist (estradiol transdermal spray), 1.53mg estradiol/spray, 0.27 fl oz (8.1 mL) per bottle, Rx Only, Manufactured for Perrigo, Minneapolis, MN 55427. NDC: 0574-2067-27

by Paddock Laboratories, LLC.

Reason
Defective Delivery System: Potential that cracks in the vial neck near the crimp may result in product evaporation and/or leaking and the inability to properly dispense product.
Published
April 4, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Indomethacin Capsules USP, 50 mg, 100-count bottle, Rx Only, Manufactured by: Glenmark Pharmaceuticals Ltd., Colvale-Bardez, Goa 403513, India; Manufactured for: Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ 07430, NDC 68462-302-01.

by Glenmark Pharmaceuticals Inc., USA

Reason
Labeling: Incorrect Instructions: bottles incorrectly labeled with the usual adult dosage of "One or two capsules 2 or 3 times a day." rather than the correct usual adult dosage of "One capsule 2 or 3 times a day.
Published
April 4, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Flucanazole Injection, USP 200 mg in in 100 mL (2 mg/mL), 10 Single Dose Flexible Containers, Rx Only, Manufactured for: Claris Lifesciences, Inc. North Brunswick, NJ 08902 By; Claris Injectables Ltd. Gujarat, India --- NDC 36000-006-10

by Renaissance Lakewood, LLC

Reason
Superpotent and Failed Stability Specifications; out of specification results for assay and water vapor permeability
Published
April 4, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Pinks Bakery Seattle, Inc.

Product
Variety Pack, Marsee Baking brand, eight 3.2oz cookies indiv…
Reason
Coconut is listed in the ingredient statement but is not declared in the Contains statement
Published
April 4, 2018
Distribution
distributed in OR and WA.

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FDA Recall United States Terminated Historical recordClass II

Pinks Bakery Seattle, Inc.

Product
Hippie Cookie, Marsee Baking brand, six 3.2oz cookies indivi…
Reason
Coconut is listed in the ingredient statement but is not declared in the Contains statement
Published
April 4, 2018
Distribution
distributed in OR and WA.

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FDA Recall United States Ongoing Historical recordClass I

Piggie Park Enterprises Inc

Product
Maurice's Honey Southern Gold BBQ Sauce; Net Wt. 18 oz. bott…
Reason
Undeclared soy and wheat ingredients
Published
April 4, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Taylor Farms California Foodservice, Inc.

Product
Taylor Farms 3/8" Diced Yellow Onion 4/5# bags - 20 lb, corr…
Reason
Firm was notified by direct customer of a confirmed positive result for Salmonella ssp. after routine testing of the diced onion product.
Published
April 4, 2018
Distribution
OK, OH, MI, MN, IA, CA, KS, WI, PA, OR,…

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FDA Recall United States Terminated Historical recordClass II

Oregon Wild Berries, Inc.

Product
Mushroom Condensed Soup, brand Chef Edwin's, packaged in gla…
Reason
Mushroom Condensed Soup, packaged in glass pint Kerr jars, is recalled due to under-processed or the venting schedule was not followed.
Published
April 4, 2018
Distribution
distributed in Oregon and Washington

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FDA Recall Terminated Historical recordClass III

Triamcinolone Acetonide Lotion, USP 0.1%, 60 mL bottle, Rx Only, Marketed by: VersaPharm Incorporated, Marietta, GA 30062; Manufactured by: Ei LLC, Kannapolis, NC 28083, NDC 61748-220-60.

by Akorn, Inc.

Reason
Failed Impurities/Degradation Specifications: High out of specification results for an impurity.
Published
March 28, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass III

Ikea North America Srvcs Inc

Product
Pink flexible, plastic package: Godis Paskkyckling Marshm…
Reason
Possible Pest Contamination at production facility.
Published
March 28, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Oregon Food Bank

Product
Roasted Pumpkin Seeds, packaged in 1 lbs. poly film bags wit…
Reason
Pumpkin seeds are recalled because the Certificate of Analysis showing a confirmed positive for Listeria species.
Published
March 28, 2018
Distribution
in Oregon and Washingon

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FDA Recall United States Terminated Historical recordClass II

Oregon Food Bank

Product
Chia Seeds packaged in poly film bags as both a twist type c…
Reason
Chia Seeds, 1 lb. packages, are recalled because they are contaminated with rodent droppings.
Published
March 28, 2018
Distribution
distributed in Oregon and Washington

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FDA Recall Terminated Historical recordClass II

Valacyclovir Tablets USP 1 gram, 30-count bottle, Rx Only, Manufactured for Camber Pharmaceuticals, Inc. Piscataway, NJ 08854 By: Hetero Hetero Labs Limit Unit V Pollypally Jadcherla Mahaboob Nagar - 509 301 India NDC # 31722-705-30

by Hetero Labs Limited Unit V

Reason
Temperature Abuse: Valganciclovir Tablets USP 450 mg and Valacyclovir Tablets USP 1 gram were exposed to higher temperature at airport or cargo and in the same consignment of Famciclovir complaint batch (D-0415-2018).
Published
March 21, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Valganciclovir Tablets, USP, 450 mg, 60-count bottle, Rx Only, Manufactured for Camber Pharmaceuticals, Inc. Piscataway, NJ 08854, By: Hetero Hetero Labs Limit Unit V Pollypally Jadcherla Mahaboob Nagar - 509 301 India. NDC # 31722-832-60

by Hetero Labs Limited Unit V

Reason
Temperature Abuse: Valganciclovir Tablets USP 450 mg and Valacyclovir Tablets USP 1 gram were exposed to higher temperature at airport or cargo and in the same consignment of Famciclovir complaint batch (D-0415-2018).
Published
March 21, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Lupin Hydrocodone Bitartrate and Homatropine Methylbromide Tablets, USP 5/1.5 mg Rx Only 30 Tablets Manufactured by: Novel Laboratories, Inc. Somerset, NJ 08873 Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, MD 21202 NDC 43386-118-03 UPC 343386118038

by Novel Laboratories, Inc.

Reason
Failed Impurities/Degradation Specifications
Published
March 21, 2018
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.