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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.

37,115
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,793
Class I recallsReasonable probability of serious health consequences
24,343
Class II recallsTemporary or medically reversible health consequences
2,887
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/so-delicious-dairy-freer-issues-voluntary-recall-salted-caramel-cluster-non-dairy-frozen-dessertPublished September 15, 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 II24,343
Class I9,793
Class III2,887
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,343
Class I9,793
Class III2,887
Not Yet Classified1

Showing 7,721–7,740 of 18,020 recalls

FDA Recall United States Terminated Historical recordClass II

Basic Reset Inc.

Product
Q-min, 50 capsules per plastic bottle, SKU: 100-9B
Reason
Products do not conform to Dietary Supplement CGMP regulations.
Published
November 27, 2019
Distribution
Product was shipped to all 50 states. Pr…

View recall →

FDA Recall United States Terminated Historical recordClass II

Basic Reset Inc.

Product
GH-C, 60 capsules per plastic bottle, SKU: 100-4F
Reason
Products do not conform to Dietary Supplement CGMP regulations.
Published
November 27, 2019
Distribution
Product was shipped to all 50 states. Pr…

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FDA Recall United States Terminated Historical recordClass II

Basic Reset Inc.

Product
Body Mass Reset, 4 fl. oz. plastic bottle, SKU: 100-8C
Reason
Products do not conform to Dietary Supplement CGMP regulations.
Published
November 27, 2019
Distribution
Product was shipped to all 50 states. Pr…

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FDA Recall United States Terminated Historical recordClass II

Basic Reset Inc.

Product
SlimUp 60 capsules per plastic bottle, SKU: 100-5B
Reason
Products do not conform to Dietary Supplement CGMP regulations.
Published
November 27, 2019
Distribution
Product was shipped to all 50 states. Pr…

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FDA Recall United States Terminated Historical recordClass II

Basic Reset Inc.

Product
Mello-Tonin 2 fl. oz. glass bottle, SKU: 100-5C
Reason
Products do not conform to Dietary Supplement CGMP regulations.
Published
November 27, 2019
Distribution
Product was shipped to all 50 states. Pr…

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FDA Recall United States Terminated Historical recordClass II

Basic Reset Inc.

Product
BETA FACTOR DIETARY SUPPLEMENT 60 capsules per plastic bott…
Reason
Products do not conform to Dietary Supplement CGMP regulations.
Published
November 27, 2019
Distribution
Product was shipped to all 50 states. Pr…

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FDA Recall United States Terminated Historical recordClass II

Basic Reset Inc.

Product
Dino Min, 60 capsules per plastic bottle, SKU: 100-1C
Reason
Products do not conform to Dietary Supplement CGMP regulations.
Published
November 27, 2019
Distribution
Product was shipped to all 50 states. Pr…

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FDA Recall United States Terminated Historical recordClass II

Basic Reset Inc.

Product
AquaLyte, 30g pkg./foil pouch, SKU: 1023
Reason
Products do not conform to Dietary Supplement CGMP regulations.
Published
November 27, 2019
Distribution
Product was shipped to all 50 states. Pr…

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FDA Recall United States Terminated Historical recordClass II

Basic Reset Inc.

Product
pH-FX 4 fl. oz. plastic bottle, SKU: 100-1A
Reason
Products do not conform to Dietary Supplement CGMP regulations.
Published
November 27, 2019
Distribution
Product was shipped to all 50 states. Pr…

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FDA Recall United States Terminated Historical recordClass II

Basic Reset Inc.

Product
Ionyte 4 fl. oz. plastic bottle, SKU: 100-1B
Reason
Products do not conform to Dietary Supplement CGMP regulations.
Published
November 27, 2019
Distribution
Product was shipped to all 50 states. Pr…

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FDA Recall United States Terminated Historical recordClass II

Basic Reset Inc.

Product
Bee Gold 8oz. pkg./plastic pouch, SKU: 100-4C
Reason
Products do not conform to Dietary Supplement CGMP regulations.
Published
November 27, 2019
Distribution
Product was shipped to all 50 states. Pr…

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FDA Recall United States Terminated Historical recordClass II

Basic Reset Inc.

Product
Vibrant ENERGY DRINK 15 g foil pouches (15 pack case) 100-…
Reason
Products do not conform to Dietary Supplement CGMP regulations.
Published
November 27, 2019
Distribution
Product was shipped to all 50 states. Pr…

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FDA Recall United States Terminated Historical recordClass II

Basic Reset Inc.

Product
Vibrant ENERGY DRINK 450 g plastic canister 100-4A
Reason
Products do not conform to Dietary Supplement CGMP regulations.
Published
November 27, 2019
Distribution
Product was shipped to all 50 states. Pr…

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FDA Recall United States Terminated Historical recordClass II

Basic Reset Inc.

Product
TRIM UP DIETARY SUPPLEMENT 80 capsules per plastic bottle,…
Reason
Products do not conform to Dietary Supplement CGMP regulations.
Published
November 27, 2019
Distribution
Product was shipped to all 50 states. Pr…

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FDA Recall Terminated Historical recordClass II

Hydrocodone Bitartrate and Homatropine Methlybromide Oral Solution 5 mg/1.5 mg per 5 mL, 473 mL bottles, Rx only, Mfd. by: KVK-Tech, Inc. Newtown PA 18940; NDC 10702-150-16

by KVK-Tech, Inc.

Reason
Presence of Foreign Substance: Black particles were found in the lots during retain sample inspection
Published
November 20, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Viatrexx-ANS/CNS, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0025, NDC 73069-039-41.

by 8046255 Canada Inc. DBA Viatrexx

Reason
Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
Published
November 20, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Viatrexx-Male+, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0400, NDC 73069-320-41.

by 8046255 Canada Inc. DBA Viatrexx

Reason
Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
Published
November 20, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Viatrexx-Neuro, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0460, NDC 73069-375-41.

by 8046255 Canada Inc. DBA Viatrexx

Reason
Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
Published
November 20, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Viatrexx-Hair, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0251, NDC 73069-206-41.

by 8046255 Canada Inc. DBA Viatrexx

Reason
Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
Published
November 20, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Viatrexx-Facial, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0184, NDC 73069-164-41.

by 8046255 Canada Inc. DBA Viatrexx

Reason
Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
Published
November 20, 2019
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.