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Recall totals

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

37,449

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,872

Class I recallsReasonable probability of serious health consequences

24,509

Class II recallsTemporary or medically reversible health consequences

2,932

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 2,096 recalls

Newest recallhttps://www.fsis.usda.gov/recalls-alerts/fsis-issues-public-health-alert-meat-and-poultry-products-due-misbranding-andPublished November 6, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated November 9, 2026 ET

Summary (Year to date)

1,956 recalls have been announced year to date.
Oct 2026 was 4% higher than the previous complete period (Sep 2026: 209).
The highest complete period was Jun 2026 (300).
Nov 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,509
Class I	9,872
Class III	2,932
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,509
Class I	9,872
Class III	2,932
Not Yet Classified	2

FDA Recall United States TerminatedTerminated: October 12, 2018Historical 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 TerminatedTerminated: November 6, 2024Historical 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 TerminatedTerminated: June 4, 2020Historical 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 TerminatedTerminated: June 4, 2020Historical 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 TerminatedTerminated: December 14, 2020Historical 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 TerminatedTerminated: April 19, 2022Historical 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 TerminatedTerminated: April 19, 2022Historical 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 TerminatedTerminated: April 19, 2022Historical 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 TerminatedTerminated: April 19, 2022Historical recordClass I