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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 October 2026.

37,269
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,852
Class I recallsReasonable probability of serious health consequences
24,397
Class II recallsTemporary or medically reversible health consequences
2,897
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 2,085 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)

  • 1,739 recalls have been announced year to date.
  • Sep 2026 was 15% higher than the previous complete period (Aug 2026: 182).
  • The highest complete period was Jun 2026 (300).
  • Oct 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 II24,397
Class I9,852
Class III2,897
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,397
Class I9,852
Class III2,897
Not Yet Classified2

Showing 981–1,000 of 20,472 recalls

FDA Recall Ongoing2026 recordClass II

Wegovy (semaglutide) Injection, 0.5 mg/0.5 mL, 4 Single-Dose Prefilled Pens, Manufactured by: Novo Nordisk A/S, DK-2880 Bagsvaerd, Denmark, Product of Denmark, Novo Nordisk A/S, Novo Nordisk Inc., Plainsboro, NJ 08536, NDC 0169-4505-14

by Novo Nordisk Inc.

Reason
Presence of Particulate Matter: Hair was found in a prefilled syringe
Published
January 7, 2026
Distribution
Nationwide

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FDA Recall Ongoing2026 recordClass II

BD ChloraPrep" Triple Swabsticks (Chlorhexidine gluconate (CHG), 2% w/v and Isopropyl alcohol (IPA), 70% v/v), 5.25 mL Applicator, CareFusion 213, LLC, El Paso, TX 79912, NDC 54365-401-29

by CareFusion 213, LLC

Reason
Lack of Assurance of Sterlity
Published
January 7, 2026
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: September 15, 20262026 recordClass II

Tom Bumble LLC

Product
Tom Bumble Nutty Peanut Butter Flake Candy with Peanut & Cho…
Reason
Foreign material.
Published
January 7, 2026
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: June 11, 20262026 recordClass III

Bendon Publishing

Product
1) Paw Patrol Heart-Shaped Gummy Candies, Mixed Fruit, Net W…
Reason
Unapproved color additive - chlorophyllin copper complex
Published
January 7, 2026
Distribution
Distributors in FL, MN, TX, WA

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FDA Recall OngoingHistorical recordClass II

Noxafil Powdermix (posaconazole) for Delayed-Release Oral Suspension, 300 mg, 8 packets per carton, Rx Only, Manufactured for: Merck Sharp & Doohme LLC, Rahway, NJ 07056 USA, Manufactured by: N.V. Organon, 5349 AB Oss, The Netherlands, a subsidiary of Organon & Co., Jersey City, NJ 07302, USA NDC 0085-2224-02.

by Merck Sharp & Dohme LLC

Reason
Presence of particulate matter: potential presence of metal particulates in the product.
Published
December 31, 2025
Distribution
Nationwide

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FDA Recall OngoingHistorical recordClass II

Merck Emend (aprepitant) for oral suspension, 125 mg, Single-Dose Kit, Rx Only, Manufactured for: Merck Sharpe & Dohme LLC, Rahway, NJ 07065, USA, Manufactured by: Novo Nordisk Production Ireland Limited Athlone, Ireland, NDC 0006-3066-03

by Merck Sharp & Dohme LLC

Reason
Presence of particulate matter: potential presence of metal particulates in the product.
Published
December 31, 2025
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: August 28, 2026Historical recordClass II

A New Life Herbs, LLC

Product
Sinus Cap Herbal Supplement, Herbs containing antibiotic, dr…
Reason
Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
Published
December 31, 2025
Distribution
Multiple states

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FDA Recall United States TerminatedTerminated: August 28, 2026Historical recordClass II

A New Life Herbs, LLC

Product
Pain Away Herbal Supplement, Analgesic & anti-inflammatory p…
Reason
Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
Published
December 31, 2025
Distribution
Multiple states

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FDA Recall United States TerminatedTerminated: August 28, 2026Historical recordClass II

A New Life Herbs, LLC

Product
Organic Ginger Root Herbal Supplement, Natural anti-inflamma…
Reason
Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
Published
December 31, 2025
Distribution
Multiple states

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FDA Recall United States TerminatedTerminated: August 28, 2026Historical recordClass II

A New Life Herbs, LLC

Product
Ear Drops Herbal Supplement, Mullein flower alcohol tincture…
Reason
Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
Published
December 31, 2025
Distribution
Multiple states

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FDA Recall United States TerminatedTerminated: August 28, 2026Historical recordClass II

A New Life Herbs, LLC

Product
Chaga Mushroom Herbal Supplement, 1:5 Alcohol Double Extract…
Reason
Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
Published
December 31, 2025
Distribution
Multiple states

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FDA Recall United States TerminatedTerminated: August 28, 2026Historical recordClass II

A New Life Herbs, LLC

Product
Boswellia Herbal Supplement, 1:5 Alcohol Double Extract, Ext…
Reason
Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
Published
December 31, 2025
Distribution
Multiple states

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FDA Recall United States TerminatedTerminated: August 28, 2026Historical recordClass II

A New Life Herbs, LLC

Product
Baby Soothe Herbal Supplement, Promotes rest, helps ease col…
Reason
Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
Published
December 31, 2025
Distribution
Multiple states

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FDA Recall United States TerminatedTerminated: August 28, 2026Historical recordClass II

A New Life Herbs, LLC

Product
Baby Allergy Herbal Supplement, Contains: Echinacea Purpurea…
Reason
Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
Published
December 31, 2025
Distribution
Multiple states

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FDA Recall United States TerminatedTerminated: August 28, 2026Historical recordClass II

A New Life Herbs, LLC

Product
Anti-virus Herbal Supplement, 1:5 Alcohol Tincture, Helps to…
Reason
Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
Published
December 31, 2025
Distribution
Multiple states

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FDA Recall United States TerminatedTerminated: January 29, 2026Historical recordClass I

Silvestri Sweets Inc dba Carousel Candies

Product
Choceur Cookie Butter Holiday Bark. Standup Pouch Bag. 5 oz.…
Reason
Undeclared pecan
Published
December 31, 2025
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: January 29, 2026Historical recordClass I

Silvestri Sweets Inc dba Carousel Candies

Product
Choceur Pecan Cranberry & Cinnamon Holiday Bark. Standup Pou…
Reason
Undeclared wheat
Published
December 31, 2025
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: May 7, 2026Historical recordClass II

Lil Turtles LLC

Product
Grandma Belle's Tomato Basil Soup, Net Wt. 17 oz. (482g), pa…
Reason
Undeclared allergen - milk
Published
December 31, 2025
Distribution
Multiple states

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FDA Recall OngoingHistorical recordClass II

Ciclopirox Shampoo, 1%, 120 mL, Rx only, Mfg by: Taro Pharmaceuticals Inc., Ontario, Canada; Dist. by: Taro Pharmaceuticals USA, Inc., NY 10532. NDC 51672-1351-08

by SUN PHARMA /TARO

Reason
Failed Impurity/Degradation specifications: OOS results obtained at the 18-month timepoint
Published
December 24, 2025
Distribution
Nationwide

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FDA Recall OngoingHistorical recordClass III

Cisatracurium Besylate Injection USP, 20 mg/10 mL*,(2 mg/mL), 10 x 10 mL Multiple-dose Vials per carton, Rx Only, Manufactured for: Somerset Therapeutics, LLC, Hollywood, FL 33024, Made in India, 10mL Multiple-dose vial, NDC 70069-161-01; 10x10mL Multiple-dose vials per Carton, NDC 70069-161-01.

by SOMERSET THERAPEUTICS LLC

Reason
Subpotent product:out of specification assay results observed during long term stability testing.
Published
December 24, 2025
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.

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