Skip to main content

Data Explorer

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.

37,115
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,793
Class I recallsReasonable probability of serious health consequences
24,343
Class II recallsTemporary or medically reversible health consequences
2,887
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.

Filters
Recall details
Location
Date range
Sort results
Clear filters
Metric
View
Recalls announced by month (Year to date)

A chart of recalls grouped by month.

Download CSV

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 II24,343
Class I9,793
Class III2,887
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,343
Class I9,793
Class III2,887
Not Yet Classified1

Showing 8,001–8,020 of 17,833 recalls

FDA Recall Terminated Historical recordClass II

Clear eyes MAXIMUM ITCHY EYE RELIEF (Glycerin 0.25%, Naphazoline hydrochloride 0.012%, Zinc Sulfate 0.25%) eye drops, 0.5 FL OZ (15 mL) bottle, Distributed by Medtech Products Inc., Tarrytown, NY 10591, A Prestige Brands Company, UPC 6 78112 65920 3.

by Medtech Products, Inc.

Reason
CGMP Deviations: concerns regarding the sufficiency of Quality Assurance controls over critical systems in the manufacturing facility that could impact the product quality of the finished products.
Published
August 28, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Clear eyes REDNESS RELIEF (Glycerin 0.25%, Naphazoline hydrochloride 0.012%) eye drops, Handy Pocket Pal, 0.2 FL OZ (6 mL) bottle, Dist. by Lil' Drug Store Products Inc., 1201 Continental Place NE, Cedar Rapids, IA 52402; Medtech Products Inc., Tarrytown, NY 10591, UPC 7 92554 70103 7.

by Medtech Products, Inc.

Reason
CGMP Deviations: concerns regarding the sufficiency of Quality Assurance controls over critical systems in the manufacturing facility that could impact the product quality of the finished products.
Published
August 28, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Clear eyes REDNESS RELIEF (Glycerin 0.25%, Naphazoline hydrochloride 0.012%) eye drops, packaged in a) 0.5 FL OZ (15 mL) bottle (UPC 6 78112 25415 6); b) 1 FL OZ (30 mL) bottle (UPC 6 78112 25419 4); c) 0.2 FL OZ (6 mL) bottle, Handy Pocket Pal (UPC 6 78112 25418 7); Distributed by Medtech Products Inc., Tarrytown, NY 10591; A Prestige Brands Company.

by Medtech Products, Inc.

Reason
CGMP Deviations: concerns regarding the sufficiency of Quality Assurance controls over critical systems in the manufacturing facility that could impact the product quality of the finished products.
Published
August 28, 2019
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

The Kroger Co

Product
PRIVATE SELECTION FROZEN BLACKBERRIES, 16 oz
Reason
Possible Hepatitis A contamination.
Published
August 28, 2019
Distribution
Product was sent to nine distributors in…

View recall →

FDA Recall United States Terminated Historical recordClass I

The Kroger Co

Product
PRIVATE SELECTION FROZEN TRIPLE BERRY MEDLEY, 16 oz
Reason
Possible Hepatitis A contamination.
Published
August 28, 2019
Distribution
Product was sent to nine distributors in…

View recall →

FDA Recall United States Terminated Historical recordClass I

The Kroger Co

Product
PRIVATE SELECTION FROZEN TRIPLE BERRY MEDLEY, 48 oz
Reason
Possible Hepatitis A contamination.
Published
August 28, 2019
Distribution
Product was sent to nine distributors in…

View recall →

FDA Recall United States Terminated Historical recordClass II

FIRST START HOLDINGS INC

Product
Nosh Organic Fruit & Protein Soft Oat Bar; Blueberry & Banan…
Reason
Fruit & Protein Soft Oat Bars have the potential to be contaminated with mold.
Published
August 28, 2019
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

FIRST START HOLDINGS INC

Product
Nosh Organic Fruit & Protein Soft Oat Bar; Apple, Sweet Pota…
Reason
Fruit & Protein Soft Oat Bars have the potential to be contaminated with mold.
Published
August 28, 2019
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Green Water, LLC

Product
Taspens Organics, Organic Tea: Mothers Milk, 2 ounce.
Reason
recalling certain lots of Bedroom Bliss Herbal Tincture, Breathe Easy Herbal Tincture, Digest Ease Herbal Tincture, Happy Momma Herbal Tincture, Mojo Magic Herbal Tincture, Respiratory Tea, Mothers Milk Tea due to potential Salmonella contamination.
Published
August 28, 2019
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Green Water, LLC

Product
Taspens Organics, Organic Tea: Respiratory, 2 ounce.
Reason
recalling certain lots of Bedroom Bliss Herbal Tincture, Breathe Easy Herbal Tincture, Digest Ease Herbal Tincture, Happy Momma Herbal Tincture, Mojo Magic Herbal Tincture, Respiratory Tea, Mothers Milk Tea due to potential Salmonella contamination.
Published
August 28, 2019
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Green Water, LLC

Product
Taspen s Organics,Mojo Magic Herbal Tincture, Net wt 1 ounce…
Reason
recalling certain lots of Bedroom Bliss Herbal Tincture, Breathe Easy Herbal Tincture, Digest Ease Herbal Tincture, Happy Momma Herbal Tincture, Mojo Magic Herbal Tincture, Respiratory Tea, Mothers Milk Tea due to potential Salmonella contamination.
Published
August 28, 2019
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Green Water, LLC

Product
Taspen s Organics,Happy Momma Herbal Tincture, Net wt 1 ounc…
Reason
recalling certain lots of Bedroom Bliss Herbal Tincture, Breathe Easy Herbal Tincture, Digest Ease Herbal Tincture, Happy Momma Herbal Tincture, Mojo Magic Herbal Tincture, Respiratory Tea, Mothers Milk Tea due to potential Salmonella contamination.
Published
August 28, 2019
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Green Water, LLC

Product
Taspen s Organics,Digest Ease Herbal Tincture, Net wt 1 ounc…
Reason
recalling certain lots of Bedroom Bliss Herbal Tincture, Breathe Easy Herbal Tincture, Digest Ease Herbal Tincture, Happy Momma Herbal Tincture, Mojo Magic Herbal Tincture, Respiratory Tea, Mothers Milk Tea due to potential Salmonella contamination.
Published
August 28, 2019
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Green Water, LLC

Product
Taspen s Organics, Breathe Easy Herbal Tincture, Net wt 1 ou…
Reason
recalling certain lots of Bedroom Bliss Herbal Tincture, Breathe Easy Herbal Tincture, Digest Ease Herbal Tincture, Happy Momma Herbal Tincture, Mojo Magic Herbal Tincture, Respiratory Tea, Mothers Milk Tea due to potential Salmonella contamination.
Published
August 28, 2019
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Green Water, LLC

Product
Taspen s Organics, Bedroom Bliss Herbal Tincture, Net wt 1 o…
Reason
recalling certain lots of Bedroom Bliss Herbal Tincture, Breathe Easy Herbal Tincture, Digest Ease Herbal Tincture, Happy Momma Herbal Tincture, Mojo Magic Herbal Tincture, Respiratory Tea, Mother s Milk Tea due to potential Salmonella contamination.
Published
August 28, 2019
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Keto Farms LLC

Product
Keto Farms Keto Snack Mix - Raspberry Gouda Fruit & Chees…
Reason
California Department of Public Health Inspection found that the allergen, coconut, was not declared on the label
Published
August 28, 2019
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Keto Farms LLC

Product
Keto Farms Keto Snack Mix - Tomato Pepperjack Fruit & Che…
Reason
California Department of Public Health Inspection found that the allergen, coconut, was not declared on the label
Published
August 28, 2019
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Keto Farms LLC

Product
Keto Farms Keto Snack Mix - Strawberry Gouda; Fruit & Chees…
Reason
California Department of Public Health Inspection found that the allergen, coconut, was not declared on the label
Published
August 28, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Tamsulosin Hydrochloride Capsules, USP 0.4 mg Rx only a) 100 count (NDC 33342-159-11), b) 500 count (NDC 33342-159-15) and c) 1000 count (NDC 33342-159-44) bottles, Manufactured : Macleods Pharma USA, Inc Plainsboro, NJ Manufactured by: Macleods Pharmaceuticals Ltd Baddi, Himchal Pradesh, INDIA

by Macleods Pharma Usa Inc

Reason
Failed Dissolution Specifications
Published
August 21, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Carbamazepine, Extended-Release Tablets, USP, 400 mg, 30 Tablets (3 blister cards x 10 unit doses), Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217. NDC Carton: 68084-562-21; NDC Unit Dose: 68084-562-11

by American Health Packaging

Reason
Failed Dissolution Specifications
Published
August 21, 2019
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.