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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.

37,066
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,786
Class I recallsReasonable probability of serious health consequences
24,313
Class II recallsTemporary or medically reversible health consequences
2,876
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/whole-foods-market-issues-allergy-alert-undeclared-egg-cabricharme-cheesePublished September 11, 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)

  • 1,527 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 II24,313
Class I9,786
Class III2,876
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,313
Class I9,786
Class III2,876
Not Yet Classified2

Showing 3,361–3,380 of 25,226 recalls

FDA Recall United States Terminated Historical recordClass II

The Coastal Companies DBA Hearn Kirkwood

Product
Egg salad sandwich packaged in clamshell for individual sale…
Reason
Tuna salad sandwich was mislabeled as an egg salad sandwich. There is an undeclared allergen of fish (Tuna).
Published
April 17, 2024
Distribution
Product was sold to institutions, hospit…

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FDA Recall United States Terminated Historical recordClass II

Taylor Farms Southwest, Inc

Product
Family Size Garden Salad 17oz packaged in Flexible plastic c…
Reason
On 03/30, TFSW ALBSWY CHICKEN CAESAR SALAD 10OZ (Egg, F-Anchovy, Milk, Soy, Wheat) was mislabeled with undeclared allergens as ALBSWY GARDEN SALAD 17OZ (Milk, Wheat)
Published
April 17, 2024
Distribution
Product was distributed to in AZ, CO, NM…

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FDA Recall United States Terminated Historical recordClass II

Taylor Farms Northwest, LLC

Product
Taylor Farms Buffalo Chicken Party Tray, packaged in black p…
Reason
Undeclared Milk, Wheat, & Soy due to incorrect ingredient label
Published
April 17, 2024
Distribution
Distributed in Oregon and Washington

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FDA Recall United States Terminated Historical recordClass I

Naturz Organics USA LLC

Product
Naturz Organics Organic Pea Protein, Item Code NO-OPP-80, Ne…
Reason
Possible salmonella contamination
Published
April 17, 2024
Distribution
Distributed to 1 consignee in WI

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FDA Recall United States Terminated Historical recordClass II

Spices USA Inc.

Product
Tasty-Sawa Cinnamon Ground, Net Wt. 55.11 lbs, paper bag (bu…
Reason
Due to elevated levels of lead in ground cinnamon
Published
April 17, 2024
Distribution
Distributors in 3 states: FL, GA, and NC…

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FDA Recall United States Terminated Historical recordClass III

Nicomex Inc.

Product
Nicomex Tequesquite, Net Wt. 1.5oz (42.52gms), UPC: 8 846781…
Reason
Elevated lead levels
Published
April 17, 2024
Distribution
Distributed to distributors in NJ, then…

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FDA Recall Terminated Historical recordClass III

Cyclophosphamide for Injection, USP, 1g/vial, Lyophilized, Single Dose Vial, Discard unused solution, Cytotoxic Agent, After Reconstitution: For direct intravenous injection or must be further diluted before intravenous infusion, Rx Only, Manufactured for: XGen Pharmaceuticals DJB, Inc., Big Flats, NY 14814, NDC # 39822-0255-01.

by X-Gen Pharmaceuticals Inc.

Reason
Labeling: Incorrect or missing Package Insert: There is an error on the Package Insert (PI), section 2.3, Preparation, Handling, and Administration. The concentration of the reconstituted product is listed as '20 mg per vial.' This information should read: '20 mg per mL'.
Published
April 10, 2024
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Cyclophosphamide for Injection, USP, 500mg/vial, Lyophilized, Cytotoxic Agent, Single Dose Vial for Intravenous Use, Rx Only, Manufactured for: XGen Pharmaceuticals DJB, Inc. Big Flats, NY 14814, NDC # 39822-0250-01.

by X-Gen Pharmaceuticals Inc.

Reason
Labeling: Incorrect or missing Package Insert: There is an error on the Package Insert (PI), section 2.3, Preparation, Handling, and Administration. The concentration of the reconstituted product is listed as '20 mg per vial.' This information should read: '20 mg per mL'.
Published
April 10, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

fentaNYL Citrate 2,500 mcg/50mL in Sterile Water, 50 mL CADD for Injection, IntegraDose Compounding Services, LLC, 719 Kasota Ave SE, Minneapolis, MN. NDC 71139-6030-1

by IntegraDose Compounding Services LLC

Reason
Lack of Assurance of Sterility: leaking bags
Published
April 10, 2024
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Lactated Ringer's Injection USP, 1000mL, EXCEL CONTAINER, Rx only, B.Braun Medical Inc., Bethlehem, PA 18018, NDC 0264-7750-00

by B. Braun Medical Inc

Reason
Lack of assurance of sterility: bags have the potential to leak..
Published
April 10, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Diltiazem Hydrochloride Extended-Release Capsules, USP 120 mg, Twice-a-Day Dosage, 100 Capsules per bottle, Rx Only, Manufactured for: Glenmark Pharmaceuticals Inc., USA Mahwah, NJ, 07430, Product of India, NDC 68462-562-01

by Glenmark Pharmaceuticals Inc., USA

Reason
Failed Dissolution Specifications: Out of Specification (OOS) was reported in test of dissolution at the 12th month time point in long term stability study.
Published
April 10, 2024
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Turkana Food Inc.

Product
Sekeroglu Lokum Love Turkish Delight With Pistachio And Pome…
Reason
Product contains Acid Red 18
Published
April 10, 2024
Distribution
Distributed to retail stores in CA, CT,…

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FDA Recall United States Terminated Historical recordClass II

Turkana Food Inc.

Product
Sekeroglu Lokum Love Turkish Delight Mixed With Pistachio An…
Reason
Product contains Acid Red 18
Published
April 10, 2024
Distribution
Distributed to retail stores in CA, CT,…

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FDA Recall United States Terminated Historical recordClass I

Kick Ash Products LLC

Product
Kick Ash Products, Door County Love Dark Chocolate Cherry Gr…
Reason
Undeclared allergen (almond) in Dark Chocolate Cherry Granola
Published
April 10, 2024
Distribution
Products were distributed Wholesale to 6…

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FDA Recall United States Terminated Historical recordClass II

AJI MORI SAUCE CORP

Product
AJI MORI***CHILLIMAMI SAUCE***UMAMI BOMB***NET WT. 250ml. Pa…
Reason
Potential contamination with Clostridium botulinum
Published
April 10, 2024
Distribution
Products were distributed direct to cons…

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FDA Recall United States Terminated Historical recordClass I

Samsung Bean Sprout

Product
Soy Bean Sprouts in a package labeled in part: Sam Sung Soy…
Reason
Listeria monocytogenes.
Published
April 10, 2024
Distribution
The product was distributed in Virgnia .

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FDA Recall United States Terminated Historical recordClass II

The Coca-Cola Company

Product
Powerade Mountain Berry Blast - 20oz PET bottles 24 vari…
Reason
The potential presence of a foreign metal object in the product, i.e. a stainless-steel ring.
Published
April 10, 2024
Distribution
U.S. distribution to 760 consignees in S…

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FDA Recall United States Terminated Historical recordClass II

The Coca-Cola Company

Product
Powerade Zero Fruit Punch - 20oz PET bottles 24 variety p…
Reason
The potential presence of a foreign metal object in the product, i.e. a stainless-steel ring.
Published
April 10, 2024
Distribution
U.S. distribution to 760 consignees in S…

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FDA Recall United States Terminated Historical recordClass II

The Coca-Cola Company

Product
Powerade Zero Mixed Berry - 20 oz PET bottles 24 variety pac…
Reason
The potential presence of a foreign metal object in the product, i.e. a stainless-steel ring.
Published
April 10, 2024
Distribution
U.S. distribution to 760 consignees in S…

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FDA Recall Ongoing Historical recordClass I

Treprostinil Injection, 20 mg/20 mL (1 mg/mL), For Subcutaneous or Intravenous Infusion Only, 20 mL Multiple-Dose Vial, Rx Only, Distributed by: Par Pharmaceutical, Chestnut Ridge, NY 10977. NDC: 42023-206-01

by Par Sterile Products LLC

Reason
Presence of Particulate Matter.
Published
April 3, 2024
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.