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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 2,581–2,600 of 21,426 recalls

FDA Recall United States Terminated Historical recordClass I

Prophet Premium Blends, LLC

Product
Diamond Shruumz Chocolate Bars Cookies & Cream UPC 755003858…
Reason
Toxic levels of muscimol
Published
August 7, 2024
Distribution
U.S. distribution to the following: AK,…

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FDA Recall United States Terminated Historical recordClass I

Prophet Premium Blends, LLC

Product
Diamond Shruumz Infused Cones Strawberry Cheesecake UPC 8101…
Reason
Toxic levels of muscimol
Published
August 7, 2024
Distribution
U.S. distribution to the following: AK,…

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FDA Recall United States Terminated Historical recordClass I

Prophet Premium Blends, LLC

Product
Diamond Shruumz Infused Cones Mint Chocolate Chip UPC 810133…
Reason
Toxic levels of muscimol
Published
August 7, 2024
Distribution
U.S. distribution to the following: AK,…

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FDA Recall United States Terminated Historical recordClass I

Prophet Premium Blends, LLC

Product
Diamond Shruumz Infused Cones Sprinkles UPC 810133320063
Reason
Toxic levels of muscimol
Published
August 7, 2024
Distribution
U.S. distribution to the following: AK,…

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FDA Recall United States Terminated Historical recordClass I

Prophet Premium Blends, LLC

Product
Diamond Shruumz Infused Cones Double Chocolate Chip UPC 8101…
Reason
Toxic levels of muscimol
Published
August 7, 2024
Distribution
U.S. distribution to the following: AK,…

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FDA Recall United States Terminated Historical recordClass I

Prophet Premium Blends, LLC

Product
Diamond Shruumz Infused Cones Cookies and Cream UPC 81013332…
Reason
Toxic levels of muscimol
Published
August 7, 2024
Distribution
U.S. distribution to the following: AK,…

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FDA Recall United States Terminated Historical recordClass III

Natural Organics, Inc.

Product
NaturesPlus T-MALE Liquid Testosterone Support for Men 8 OZ…
Reason
Product is missing the ingredient TongKat Ali and has additional Rhodiola Rosea
Published
August 7, 2024
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass III

Natural Organics, Inc.

Product
NaturesPlus ULTRA T-MALE Maximum Strength Testosterone Boost…
Reason
Product is missing the ingredient TongKat Ali and has additional Rhodiola Rosea
Published
August 7, 2024
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Complete 30C/200C Homeopathic Kit, Contains: One hundred 1/2 dram vials of homeopathic medicines, Washington Homeopathic Products, Inc., Berkley Springs, WV 25411, UPC 7 40640 64300 6.

by Washington Homeopathic Products, Inc.

Reason
Labeling: Label Mix-up: Some bottles of Ferrum Phosphoricum 200C were incorrectly labeled as Ferrum Metallicum 200C.
Published
July 31, 2024
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Venlafaxine Hydrochloride Extended-Release Capsules, USP 37.5mg, packaged in a) 90-count bottles (NDC 68382-034-16) and b)1000-count bottles (NDC 68382-034-10), Rx only, Mfg. by: Zydus Lifesciences Ltd. Ahmedabad, India; Dist. by: Zydus Pharmaceuticals (USA) Inc. Pennington, NJ 08534

by Zydus Pharmaceuticals (USA) Inc

Reason
Failed Dissolution Specifications: Out-of-specification results observed for dissolution testing at the 8-hour and 12-hour pull intervals.
Published
July 31, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass III

Hemp Bombs CBD Pain Freeze (menthol 4%), 1000mg, 4 oz bottles, Distributed by: Global Widget 8419 Sunstate St, Tampa FL 33634; UPC Code: 8-40078-56612-7

by GLOBAL WIDGET LLC

Reason
Subpotent drug: The potency of the active (menthol) was less than the label claim of 4%.
Published
July 31, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass III

Hemp Bombs CBD Pain Freeze (menthol 4%), 400mg, 4 oz bottles, Distributed by: Global Widget 8419 Sunstate St, Tampa FL 33634; UPC code: 8-40078-56497-0

by GLOBAL WIDGET LLC

Reason
Subpotent drug: The potency of the active (menthol) was less than the label claim of 4%.
Published
July 31, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass III

Nature's Script CBD Cryotherapy Pain Relief Roll on (menthol 4%) 200mg, 1 oz bottles, Distributed by: Global Widget 8419 Sunstate St, Tampa FL 33634, UPC code: 8-40078-56731-5

by GLOBAL WIDGET LLC

Reason
Subpotent drug: The potency of the active (menthol) was less than the label claim of 4%.
Published
July 31, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass III

Hemp Bombs CBD Pain Freeze (menthol 4%), 100mg, 1 oz bottles, Distributed by: Global Widget 8419 Sunstate St, Tampa FL 33634, NDC 73423-003-01; UPC Code: 8-40078-56493-2

by GLOBAL WIDGET LLC

Reason
Subpotent drug: The potency of the active (menthol) was less than the label claim of 4%.
Published
July 31, 2024
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Canadian Art Prints

Product
UPC 772665860106. PLT010. Indigenous Collection Signature Pl…
Reason
Glazed ceramic plates are recalled because they may exceed FDA guidance levels for leachable lead (3.0mg/L).
Published
July 31, 2024
Distribution
Distributed in AK, AZ, CA, GA, ID, IL, M…

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FDA Recall United States Terminated Historical recordClass II

Canadian Art Prints

Product
UPC Code 772665860083, Stock code PLT008, Indigenous Collect…
Reason
Glazed ceramic plates are recalled because they may exceed FDA guidance levels for leachable lead (3.0mg/L).
Published
July 31, 2024
Distribution
Distributed in AK, AZ, CA, GA, ID, IL, M…

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FDA Recall Ongoing Historical recordClass II

Pravastatin Sodium Tablets, USP 80mg, packaged in a) 90-count bottle, NDC 68462-198-90; b) 500-count bottle, NDC 68462-198-05, Rx only, Manufactured by: Glenmark Pharmaceuticals Limited Pithampur, Madhya Pradesh 454775, India, Manufactured for: Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ 07430,

by Glenmark Pharmaceuticals Inc., USA

Reason
Failed Dissolution Specifications: results below specifications
Published
July 24, 2024
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Potassium Chloride Micro 10mEq K (750 mg) Extended Release Capsules, 30-count blister card, Rx only, MFG: Glenmark, Mahwah, NJ 07430, Repackaged by: RemedyRepack Inc., Indiana, PA 15701, NDC 70518-1203-03

by RemedyRePack Inc.

Reason
CGMP Deviations: Out of specification for dissolution
Published
July 24, 2024
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

STELLALIFE ADVANCED FORMULA Peppermint, VEGA Oral Care, Rinse, 16 fl oz (473 ml), Distributed by: StellaLife, 2875 NE 191 Street, Suite 500, Aventura, FL 33180, NDC 69685-143-16

by Homeocare Laboratories, Inc.

Reason
Microbial Contamination of Non-Sterile Products: presence of Terribacillus species organism
Published
July 24, 2024
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

STELLALIFE VEGA Oral Care, Spray, Unflavored, 1 fl oz (30 ml) bottles, Distributed by: StellaLife, 22875 NE 191 Street, Suite 500, Aventura, FL 33180, NDC 69685-121-01

by Homeocare Laboratories, Inc.

Reason
Microbial Contamination of Non-Sterile Products: multiple Bacillus species organisms
Published
July 24, 2024
Distribution
Nationwide

View recall →

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.