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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.

37,343
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,860
Class I recallsReasonable probability of serious health consequences
24,450
Class II recallsTemporary or medically reversible health consequences
2,901
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 2,095 recalls
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/vitality-works-inc-recalls-365-whole-foods-market-ashwagandha-capsules-sold-nationwide-due-potentialPublished October 30, 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)

  • 1,739 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 II24,450
Class I9,860
Class III2,901
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,450
Class I9,860
Class III2,901
Not Yet Classified2

Showing 3,201–3,220 of 21,274 recalls

FDA Recall OngoingHistorical recordClass I

Neptune's Fix, Tianeptine Extra Strength Elixir, 0.338 fl oz (10 mL) bottle, Distributed By Neptune Resources, LLC, 30 N. Gould Street, Ste R, Sheridan, WY 82801.

by Neptune Resources, LLC

Reason
Marketed without an approved NDA/ANDA: Product contains tianeptine, a substance not FDA-approved for any medical use in the United States.
Published
February 28, 2024
Distribution
Nationwide

View recall →

FDA Recall OngoingHistorical recordClass I

Neptune's Fix, Tianeptine Elixir, Fast Acting, 0.338 fl oz (10 mL) bottle, Distributed By Neptune Resources, LLC, 30 N. Gould Street, Ste R, Sheridan, WY 82801.

by Neptune Resources, LLC

Reason
Marketed without an approved NDA/ANDA: Product contains tianeptine, a substance not FDA-approved for any medical use in the United States.
Published
February 28, 2024
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: February 9, 2026Historical recordClass II

Equate Cherry Cough Drops, Menthol cough suppressant/Oral Anesthetic, a) 30 drops per bag, item number 20000462, b) 160 drops per bag, item number 20000463, Bestco, 288 Mazeppa Road, Mooresville, NC 28115

by Bestco LLC

Reason
CGMP Deviations: Potential Glass and Silicone particulates in product
Published
February 28, 2024
Distribution
Nationwide

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FDA Recall TerminatedTerminated: February 9, 2026Historical recordClass II

Family Wellness Cherry Cough Drops Menthol cough suppressant/Oral Anesthetic, 80 drops per bag, item number 20001187, Bestco, 288 Mazeppa Road, Mooresville, NC 28115

by Bestco LLC

Reason
CGMP Deviations: Potential Glass and Silicone particulates in product
Published
February 28, 2024
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: February 9, 2026Historical recordClass II

Kroger Cherry Cough Drops, Menthol cough suppressant/Oral Anesthetic, 200 drops per bag, item number 20000064, Bestco, 288 Mazeppa Road, Mooresville, NC 28115

by Bestco LLC

Reason
CGMP Deviations: Potential Glass and Silicone particulates in product
Published
February 28, 2024
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: February 9, 2026Historical recordClass II

Meijer Cherry Cough Drops, Menthol cough suppressant/Oral Anesthetic, 200 drops per bag, item number 20000345, Bestco, 288 Mazeppa Road, Mooresville, NC 28115

by Bestco LLC

Reason
CGMP Deviations: Potential Glass and Silicone particulates in product
Published
February 28, 2024
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: February 9, 2026Historical recordClass II

CVS Health Cherry Cough Drops, Menthol cough suppressant/Oral Anesthetic, 160 drops per bag, item number 20001089, Bestco, 288 Mazeppa Road, Mooresville, NC 28115

by Bestco LLC

Reason
CGMP Deviations: Potential Glass and Silicone particulates in product
Published
February 28, 2024
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: February 14, 2025Historical recordClass II

Oseltamivir Phosphate for Oral Suspension 6mg/ml, 60 mL (reconstituted) bottle, RX only, Distributed by Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807. NDC# 69238-1273-6

by Amneal Pharmaceuticals of New York, LLC

Reason
Failed Impurities/Degradation Specifications: Out-of-specification test results.
Published
February 28, 2024
Distribution
Nationwide

View recall →

FDA Recall OngoingHistorical recordClass II

Fluticasone Propionate Nasal Spray USP 50mcg, 120 Metered Sprays - 16 g net fill, Rx Only, Manufactured by: Apotex Inc. Toronto, Ontario Canada M9L 1T9, Manufactured for: Apotex Corp Weston, FL 33326. NDC 60505-0829-1

by Apotex Corp.

Reason
CGMP Deviations: potential presence of Burkholderia cepacia complex
Published
February 28, 2024
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: March 25, 2024Historical recordClass II

Country Corner Dairy, LLC

Product
Fresh Local , Country Corner Dairy, SIZZLING COLBY CHEESE,…
Reason
Product was made with a lack of proper pasteurization.
Published
February 28, 2024
Distribution
The recall product was distributed to th…

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FDA Recall United States TerminatedTerminated: March 25, 2024Historical recordClass II

Country Corner Dairy, LLC

Product
Fresh Local , Country Corner Dairy, YELLOW CHEDDAR CHEESE,…
Reason
Product was made with a lack of proper pasteurization.
Published
February 28, 2024
Distribution
The recall product was distributed to th…

View recall →

FDA Recall United States TerminatedTerminated: March 25, 2024Historical recordClass II

Country Corner Dairy, LLC

Product
Fresh Local , Country Corner Dairy, YELLOW COLBY CHEESE, IN…
Reason
Product was made with a lack of proper pasteurization.
Published
February 28, 2024
Distribution
The recall product was distributed to th…

View recall →

FDA Recall United States TerminatedTerminated: March 25, 2024Historical recordClass II

Country Corner Dairy, LLC

Product
Fresh Local , Country Corner Dairy, WHITE COLBY CHEESE, INGR…
Reason
Product was made with a lack of proper pasteurization.
Published
February 28, 2024
Distribution
The recall product was distributed to th…

View recall →

FDA Recall United States TerminatedTerminated: March 25, 2024Historical recordClass II

Country Corner Dairy, LLC

Product
Fresh Local , Country Corner Dairy, WHITE CHEDDAR CHEESE, IN…
Reason
Product was made with a lack of proper pasteurization.
Published
February 28, 2024
Distribution
The recall product was distributed to th…

View recall →

FDA Recall United States TerminatedTerminated: November 21, 2025Historical recordClass II

The Procter & Gamble Company

Product
Meta Psyllium Fiber Capsules packaged as 100 count or 160 co…
Reason
Illegible Label
Published
February 28, 2024
Distribution
Alabama, Arizona, Arkansas, California,…

View recall →

FDA Recall TerminatedTerminated: December 22, 2025Historical recordClass II

HydrALAZINE Hydrochloride Tablets, USP 10mg, packaged in 100-count (10x10 blister cards), Lot T04680, Rx only, Manufactured for Heritage Pharmaceuticals, Inc. Eatontown, NJ, Distributed by Major Pharmaceuticals Livonia MI. NDC 0904-6440-61

by The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Reason
an out of specification result obtained during routine stability testing for Impurities. There is a remote possibility that use of this product could cause a medically reversible or transient adverse health consequences.
Published
February 21, 2024
Distribution
Nationwide

View recall →

FDA Recall OngoingHistorical recordClass III

Nortrel 7/7/7 (norethindrone and ethinyl estradiol tablets USP- triphasic regimen), packaged in cartons, each carton contains 6 blister cards, each card contains 28 tablets, Rx only, TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454, NDC 0555-9012-58

by Teva Pharmaceuticals USA, Inc

Reason
Discoloration: discolored tablets (shades of blue) mixed in with the white inert remainder tablets.
Published
February 21, 2024
Distribution
Nationwide

View recall →

FDA Recall OngoingHistorical recordClass III

Nortrel (norethindrone and ethinyl estradiol tablets USP) 0.5/35, packaged in cartons, each carton contains 3 blister cards, each card contains 28 tablets, Rx only, TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454, NDC 0555-9008-67

by Teva Pharmaceuticals USA, Inc

Reason
Discoloration: discolored tablets (shades of blue) mixed in with the white inert remainder tablets.
Published
February 21, 2024
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: April 19, 2024Historical recordClass II

UNFI General Corporate

Product
Woodstock 5 Grain Cereal. Oats, Rye, Triticale, Barley, Gol…
Reason
The ingredient Triticale is not identified as wheat.
Published
February 21, 2024
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: August 23, 2024Historical recordClass I

U.S. Tov, Inc.

Product
Dragonfly Jelly Bar Handbag 11.64oz, 17.63oz UPC Code 721557…
Reason
Potential choking hazard; product contains konjac.
Published
February 21, 2024
Distribution
U.S. distribution to the following: AK,…

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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