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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.

37,142
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 11,601–11,620 of 19,943 recalls

FDA Recall United States Terminated Historical recordClass I

eBars

Product
FOCUS ORGANIC CHOCOLATE PEANUT bar NET WT. 1.6 OZ (45g) Manu…
Reason
The firm was notified by the State of TN that the product contained undeclared almonds.
Published
May 23, 2018
Distribution
Product was shipped to the following sta…

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FDA Recall United States Terminated Historical recordClass I

eBars

Product
FIT ORGANIC PEANUT BUTTER CHOCOLATE RASPBERRY bar NET WT 1.8…
Reason
The firm was notified by the State of TN that the product contained undeclared almonds.
Published
May 23, 2018
Distribution
Product was shipped to the following sta…

View recall →

FDA Recall United States Terminated Historical recordClass I

eBars

Product
DIABEATIC Chocolate Berry Crunch bar NET WT 1.4 oz (42g)Manu…
Reason
The firm was notified by the State of TN that the product contained undeclared peanuts.
Published
May 23, 2018
Distribution
Product was shipped to the following sta…

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FDA Recall Terminated Historical recordClass I

Ampicillin and Sulbactam for Injection, USP, 3 gram*s/vial, For Intramuscular or Intravenous Use, Sterile, Manufactured for: AuroMedics Pharma LLC, 6 Wheeling Road, Dayton, NJ, NDC 55150-117-20.

by AuroMedics Pharma LLC

Reason
Presence of Particulate Matter: confirmed customer report of the presence of visible particulate matter believed to be red rubber particles from the manufacturing process of the active ingredients.
Published
May 16, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Minivelle (estradiol transdermal system) 0.0375 mg/day, 1 System per pouch (NDC 68968-6637-1), packaged in 8 pouches per box (NDC 68968-6637-8), Rx only, Mfd. by: Noven Pharmaceuticals, Inc., Miami, Florida 33186; Dist. by: Noven Therapeutics, LLC, Miami, Florida 33186.

by Noven Pharmaceuticals, Inc.

Reason
Defective Delivery System: no longer meets the specification for shear, an attribute related to the adhesive properties of the transdermal patches. As a result, patients could experience patches that do not stick well to the skin.
Published
May 16, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Minivelle (estradiol transdermal system) 0.1 mg/day, 1 System per pouch (NDC 68968-6610-1), packaged in 8 pouches per box (NDC 68968-6610-8), Rx only, Mfd. by: Noven Pharmaceuticals, Inc., Miami, Florida 33186; Dist. by: Noven Therapeutics, LLC, Miami, Florida 33186.

by Noven Pharmaceuticals, Inc.

Reason
Defective Delivery System: no longer meets the specification for shear, an attribute related to the adhesive properties of the transdermal patches. As a result, patients could experience patches that do not stick well to the skin.
Published
May 16, 2018
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Metoprolol Succinate Extended-Release Tablets, USP, 100 mg, 100 Tablets bottle, Rx only, Manufactured by: Dr. Reddy's Laboratories Limited Bachupally-500 090 India\ NDC 55111-468-01

by Dr. Reddy's Laboratories, Inc.

Reason
Presence of Foreign Tablets/Capsules: One foreign tablet identified as Clopidogrel 75 mg was found in a 100 count bottle of Metoprolol Succiante Extended-Release Tablets.
Published
May 16, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Badger Botanicals LLC

Product
Acadica Kratom: Green Hulu 2 Kratom, 250g bags
Reason
Recalling Red Suma, Green Suma, Red Hulu 2, Green Hulu 2 Kratom products due to potential salmonella.
Published
May 16, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Badger Botanicals LLC

Product
Acadica Kratom: Red Hulu 2, 250g bags
Reason
Recalling Red Suma, Green Suma, Red Hulu 2, Green Hulu 2 Kratom products due to potential salmonella.
Published
May 16, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Badger Botanicals LLC

Product
Acadica Kratom: Green Suma, 250g bags
Reason
Recalling Red Suma, Green Suma, Red Hulu 2, Green Hulu 2 Kratom products due to potential salmonella.
Published
May 16, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Badger Botanicals LLC

Product
Acadica Kratom: Red Suma 250g bags
Reason
Recalling Red Suma, Green Suma, Red Hulu 2, Green Hulu 2 Kratom products due to potential salmonella.
Published
May 16, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Stonewall Kitchen, LLC

Product
STONEWALL KITCHEN Basil Pesto Aioli Net Weight Net 10.25 oz.…
Reason
Product may contain undeclared eggs.
Published
May 16, 2018
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

TRIANGLE PHARMANATURALS LLC

Product
Third Eye Kratom Bali in 300 capsule plastic bottles. Ma…
Reason
All Kratom products manufactured, processed, packed, and/or held by Triangle Pharmanaaturals LLC have the potential to be contaminated with Salmonella
Published
May 16, 2018
Distribution
WA, GA, SC, FL, NJ, LA, CA, TX, NV, NC,…

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FDA Recall United States Terminated Historical recordClass I

TRIANGLE PHARMANATURALS LLC

Product
Third Eye Kratom Red in 300 capsule plastic bottles. Man…
Reason
All Kratom products manufactured, processed, packed, and/or held by Triangle Pharmanaaturals LLC have the potential to be contaminated with Salmonella
Published
May 16, 2018
Distribution
WA, GA, SC, FL, NJ, LA, CA, TX, NV, NC,…

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FDA Recall United States Terminated Historical recordClass I

TRIANGLE PHARMANATURALS LLC

Product
Third Eye Kratom White in 300 capsule plastic bottles; Ma…
Reason
All Kratom products manufactured, processed, packed, and/or held by Triangle Pharmanaaturals LLC have the potential to be contaminated with Salmonella
Published
May 16, 2018
Distribution
WA, GA, SC, FL, NJ, LA, CA, TX, NV, NC,…

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FDA Recall United States Terminated Historical recordClass I

TRIANGLE PHARMANATURALS LLC

Product
Live Well Kratom Red Maeng Da in 150 capsule and 300 capsule…
Reason
All Kratom products manufactured, processed, packed, and/or held by Triangle Pharmanaaturals LLC have the potential to be contaminated with Salmonella
Published
May 16, 2018
Distribution
WA, GA, SC, FL, NJ, LA, CA, TX, NV, NC,…

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FDA Recall United States Terminated Historical recordClass I

TRIANGLE PHARMANATURALS LLC

Product
Live Well Kratom Green Maeng Da in 150 capsule and 300 capsu…
Reason
All Kratom products manufactured, processed, packed, and/or held by Triangle Pharmanaaturals LLC have the potential to be contaminated with Salmonella
Published
May 16, 2018
Distribution
WA, GA, SC, FL, NJ, LA, CA, TX, NV, NC,…

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FDA Recall United States Terminated Historical recordClass I

TRIANGLE PHARMANATURALS LLC

Product
Lifted Kratom Gold Bali in 45 gram powder, 150 capsule and 3…
Reason
All Kratom products manufactured, processed, packed, and/or held by Triangle Pharmanaaturals LLC have the potential to be contaminated with Salmonella
Published
May 16, 2018
Distribution
WA, GA, SC, FL, NJ, LA, CA, TX, NV, NC,…

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FDA Recall United States Terminated Historical recordClass I

TRIANGLE PHARMANATURALS LLC

Product
Lifted Kratom Green Maeng Da in 45 gram powder, 150 capsule…
Reason
All Kratom products manufactured, processed, packed, and/or held by Triangle Pharmanaaturals LLC have the potential to be contaminated with Salmonella
Published
May 16, 2018
Distribution
WA, GA, SC, FL, NJ, LA, CA, TX, NV, NC,…

View recall →

FDA Recall United States Terminated Historical recordClass I

TRIANGLE PHARMANATURALS LLC

Product
Lifted Kratom Red Maeng Da in 45 gram powder, 150 capsule an…
Reason
All Kratom products manufactured, processed, packed, and/or held by Triangle Pharmanaaturals LLC have the potential to be contaminated with Salmonella
Published
May 16, 2018
Distribution
WA, GA, SC, FL, NJ, LA, CA, TX, NV, NC,…

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.