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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.

37,059
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,786
Class I recallsReasonable probability of serious health consequences
24,313
Class II recallsTemporary or medically reversible health consequences
2,876
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 II24,313
Class I9,786
Class III2,876
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,313
Class I9,786
Class III2,876
Not Yet Classified2

Showing 1,161–1,180 of 17,805 recalls

FDA Recall United States Ongoing Historical recordClass II

Tropicale Foods, LLC

Product
Helados Mexico Minis Variety Paletas 12-Count 18oz UPC:6-820…
Reason
Product label includes the ingredient CREAM but does not include Milk as the source.
Published
August 20, 2025
Distribution
Nationwide

View recall →

FDA Recall United States Ongoing Historical recordClass II

Tropicale Foods, LLC

Product
Helados Mexico Minis Variety Paletas 12-Count 18oz UPC: 6-82…
Reason
Product label includes the ingredient CREAM but does not include Milk as the source.
Published
August 20, 2025
Distribution
Nationwide

View recall →

FDA Recall United States Ongoing Historical recordClass II

Tropicale Foods, LLC

Product
La Michoacana Variety Paletas 16-Count 44oz UPC:7-67778-0310…
Reason
Product label includes the ingredient CREAM but does not include Milk as the source.
Published
August 20, 2025
Distribution
Nationwide

View recall →

FDA Recall United States Ongoing Historical recordClass II

Tropicale Foods, LLC

Product
La Michoacana Minis Variety Paletas 12-Count 16.5oz UPC: 7-6…
Reason
Product label includes the ingredient CREAM but does not include Milk as the source.
Published
August 20, 2025
Distribution
Nationwide

View recall →

FDA Recall United States Ongoing Historical recordClass II

Tropicale Foods, LLC

Product
La Michoacana Coconut Con Crema 6-Pack Paleta 16.5oz UPC: 7-…
Reason
Product label includes the ingredient CREAM but does not include Milk as the source.
Published
August 20, 2025
Distribution
Nationwide

View recall →

FDA Recall United States Ongoing Historical recordClass II

Tropicale Foods, LLC

Product
La Michoacana Bubble Gum Single Serve Paleta 3.75oz UPC: 7-6…
Reason
Product label includes the ingredient CREAM but does not include Milk as the source.
Published
August 20, 2025
Distribution
Nationwide

View recall →

FDA Recall United States Ongoing Historical recordClass II

Tropicale Foods, LLC

Product
La Michoacana Strawberry Con Crema Single Serve Paleta 3.75o…
Reason
Product label includes the ingredient CREAM but does not include Milk as the source.
Published
August 20, 2025
Distribution
Nationwide

View recall →

FDA Recall United States Ongoing Historical recordClass II

Tropicale Foods, LLC

Product
La Michoacana Coconut Con Crema Single Serve Paleta 3.75oz U…
Reason
Product label includes the ingredient CREAM but does not include Milk as the source.
Published
August 20, 2025
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass III

Enjoy Nutrition, LLC; dba Weyland Brain Nutrition

Product
Lithium Orotate, 10MG, Distributed by Enjoy Nutrition, LLC.…
Reason
Under potency / misbranding: product fails to meet labeled lithium orotate potency. (Downstream recall) from supplier of ingredient.
Published
August 20, 2025
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass III

Enjoy Nutrition, LLC; dba Weyland Brain Nutrition

Product
Lithium Orotate, 5MG, Distributed by Enjoy Nutrition, LLC. U…
Reason
Under potency / misbranding: product fails to meet labeled lithium orotate potency. (Downstream recall) from supplier of ingredient.
Published
August 20, 2025
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Superior Foods Company

Product
Park Street Deli Cinnamon Bun Dessert Dip Net WT 7oz. in pla…
Reason
foreign material (plastic)
Published
August 20, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Spironolactone Tablets, USP, 25 mg, 100-count bottle, Rx only, Mfg. by: Frontida BioPharm, Inc., 1100 Orthodox St, Philadelphia, PA 19124, Dist. by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, NDC 53489-143-01

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason
Presence of foreign substance: identified as aluminum.
Published
August 13, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

RECOMBINATE, [Antihemophilic Factor (Recombinant)], 5 mL vials, Rx Only, Takeda Pharmaceuticals USA, Cambridge, MA 02142, NDC: 00944-2843-01

by Cardinal Health Inc.

Reason
CGMP Deviations - Product was exposed to temperatures outside the product's labeled storage requirements.
Published
August 13, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Xolair (omalizumab injection), 75 mg/0.5 ml, Rx only, Genentech, Inc., South San Francisco, CA 94080, NDC 50242-214-55

by Cardinal Health Inc.

Reason
CGMP Deviations - Product was exposed to temperatures outside the product's labeled storage requirements.
Published
August 13, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Xolair (omalizumab injection), 150 mg/ml, 1 auto-injector, Rx only, Genentech, Inc, South San Francisco, CA 9408, NDC: 50242-215-55.

by Cardinal Health Inc.

Reason
CGMP Deviations - Product was exposed to temperatures outside the product's labeled storage requirements.
Published
August 13, 2025
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Duloxetine D/R, 30 mg, 30 Caps, RX Only, Packaged as a) 30-count bottle NDC 61919-0482-30, b) 60-count bottle, NDC 61919-0482-60, c) 90-count bottle, NDC 61919-0482-90; Packaged & Distributed by: Direct Rx, Dist. By Breckenridge Pharm., Inc., Berlin, CT 06037,

by Direct Rx

Reason
CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity above the proposed interim limit.
Published
August 13, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Duloxetine D/R, 20 mg, 30 Caps, 30-count bottle, RX Only, Packaged & Distributed by: Direct Rx, Dist. By Breckenridge Pharm., Inc., Berlin, CT 06037, NDC 61919-422-30

by Direct Rx

Reason
CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity above the proposed interim limit.
Published
August 13, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Doxepin Hydrochloride Capsules, USP, 10 mg, 100 Capsules, Rx only, Manufactured by: Alembic Pharmaceuticals Limited, Panela v 389350, Gujarat, India, Manufactured for: Alembic Pharmaceuticals, Inc., Bedminster, NJ 07921, USA, NDC 62332-637-31

by Alembic Pharmaceuticals Limited

Reason
CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity above the proposed interim limit.
Published
August 13, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Duloxetine Delayed-Release Capsules, USP, 60mg, 1,000-count bottles, Rx Only, Mfr. by: Towa Pharmaceutical Europe, S.L. Martorelles, (Barcelona), Spain, Distributed by: Breckenridge Pharmaceuticals, Inc., Berkeley Heights, NJ 07922. NDC 51991-748-10.

by Breckenridge Pharmaceutical, Inc.

Reason
CGMP Deviations: Presence of N-nitroso-duloxetine impurity above safety assessment limit
Published
August 13, 2025
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

QUEEN BEE GARDENS

Product
Brand Name: Queen Bee Gardens Whipped Honey Huckleberry Inte…
Reason
Product may have small flakes of stainless steel in product.
Published
August 13, 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.