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Recall totals

All FDA and USDA recalls in Public Health Trace, June 2012 to September 2026.

37,204

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,841

Class I recallsReasonable probability of serious health consequences

24,366

Class II recallsTemporary or medically reversible health consequences

2,892

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 2,073 recalls

Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/sierra-nevada-cheese-company-recalls-graziers-raw-milk-cheese-because-possible-health-riskPublished September 28, 2026

Most affected stateHawaii 200 recalls mention this state

State: OH ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated October 1, 2026 ET

Summary (Year to date)

1,714 recalls have been announced year to date.
Sep 2026 was 3% higher than the previous complete period (Aug 2026: 182).
The highest complete period was Jun 2026 (297).
Oct 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,366
Class I	9,841
Class III	2,892
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,366
Class I	9,841
Class III	2,892
Not Yet Classified	2

FDA Recall United States Terminated Historical recordClass I

eBars

Product: GOLF ORGANIC DARK COCOA RASPBERRY bar NET WT. 1.6 OZ (45g) M…
Reason: The product test positive for peanut allergen which is not declared on the product label.
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: GOLF ORGANIC CHOCOLATE ALMONDS bar NET WT. 1.6 OZ (45g) Manu…
Reason: The product test positive for peanut allergen which is not declared on the product label.
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: FOCUS FOR KIDS! SUNFLOWER SEED CHOCOLATE STRAWBERRY bar NET…
Reason: The product test positive for peanuts and almond allergen which is not declared on the product label.
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: 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…

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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 United States Terminated Historical recordClass II

Kanan Enterprises, Inc.

Product: Market District Roasted Salted Cashews Whole Fancy Net WT 26…
Reason: The firm was notified by a customer that the product contains almonds and pecans that are not listed in the ingredient statement.
Published: May 23, 2018
Distribution: Product was shipped to Ohio and Pennsylv…

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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

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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

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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Data last updated: October 1, 2026 ET

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.