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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.

37,060
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
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/freshpoint-issues-recall-due-improperly-declared-allergen-egg-chicken-salad-wedge-sandwichesPublished September 8, 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)

  • 1,527 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 1,621–1,640 of 18,528 recalls

FDA Recall United States Terminated Historical recordClass II

FGF, LLC

Product
item 8201805 APPLE FRITTER 60x2.5 OZ, NET WT 8.44 LB
Reason
potential for contamination with listeria monocytogenes
Published
February 12, 2025
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

FGF, LLC

Product
item 8201804 Yeast Ring Donut 108x2.15OZ, NET WT 13.06 LB
Reason
potential for contamination with listeria monocytogenes
Published
February 12, 2025
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

FGF, LLC

Product
item 8201780 GEN CHOC CK DONUT RINGS PFD 90x2.5OZ, NET WT12.…
Reason
potential for contamination with listeria monocytogenes
Published
February 12, 2025
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

FGF, LLC

Product
item 8201779 GEN PLN CAKE DONUT RINGS PFD 90x2.5 OZ, NET WT…
Reason
potential for contamination with listeria monocytogenes
Published
February 12, 2025
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Monkey Spit

Product
Monkey Spit "Monkey Mop" BBQ Sauce, 12 fl oz (355ml) glass b…
Reason
Barbeque sauce product contains undeclared listing of (Milk) in product ingredient listing from sub-ingredient Butter.
Published
February 12, 2025
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Monkey Spit

Product
Monkey Spit "Atomic Mop" BBQ Sauce, 12 fl oz (355ml) glass b…
Reason
Barbeque sauce product contains undeclared allergen listing of (Milk) in product ingredient listing from sub-ingredient Butter.
Published
February 12, 2025
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Monkey Spit

Product
Monkey Spit "Swamp Mop" BBQ Sauce, 12 fl oz (355ml) glass bo…
Reason
Barbeque sauce product contains undeclared allergens (soy) contained in sub-ingredient
Published
February 12, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Inflectra (infliximab-dyyb), For injection, 100mg per vial, packaged in 10 mL single-dose vial, Rx only, Mfd by: CELLTRION, INC, Dist. by: Pfizer Labs, Division of Pfizer Inc., New York, NY 10001, NDC 0069-0809-01

by McKesson

Reason
cGMP Deviations: Product intended for quarantine was inadvertently distributed.
Published
February 5, 2025
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Duloxetine Delayed-Release Capsules USP, 20 mg, packaged in a) 30 Unit Doses (3x10 blister packs) NDC 0904-7043-04 and b) 100 Unit Doses (10x10 blister packs) NDC 0904-7043-61, Rx only, Packaged and Distributed by: Major Pharmaceuticals, Indianapolis, IN 46268 USA.

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

Reason
CGMP Deviations: presence of Nitrosamine Drug Substances Related Impurity (NDSRI), N-Nitroso-Duloxetine above the FDA recommended acceptable intake limit
Published
February 5, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass I

Prograf (tacrolimus) capsules, USP, 0.5 mg, 100-count bottle, Rx Only, Product of Japan, Distributed by: Astellas Pharma US, Inc., Northbrook, IL 60062, NDC 0469-0607-73.

by Astellas Pharma US Inc.

Reason
Failed Tablet/Capsule Specifications: Bottles shipped to the USA may contain empty capsules
Published
February 5, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass I

Astagraf XL (tacrolimus extended-release capsules) 0.5 mg, 30-count bottles, RX Only, Product of Japan, Distributed by: Astellas Pharma US Inc., Northbrook, IL 60062, NDC 0469-0647-73.

by Astellas Pharma US Inc.

Reason
Failed Tablet/Capsule Specifications: Bottles shipped to the USA may contain empty capsules
Published
February 5, 2025
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

BADGER 50, ADVENTURE SPORT MINERAL SUNSCREEN WITH CLEAR ZINC, (uncoated 25% zinc oxide), 2.4 oz., Tin, W.S. Badger Company, Inc, 768 Route 10, Gilsum NH, 03448 UPC 6 34084 47150 2

by The W.S. Badger Company, Inc.

Reason
Labeling: Missing Label: The finished product potentially missing the labeling with the drug facts panel, bar code and directions for use.
Published
February 5, 2025
Distribution
Nationwide

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FDA Recall United States Completed Historical recordClass II

BakeMark USA LLC.

Product
WESTCO 3065 GOLDEN BAVARIAN CREME FILLING ARTIFICIALLY FLAVO…
Reason
Scheduled process deviation: Final pH of 4.61, 4.66, 4.69, 4.67.
Published
February 5, 2025
Distribution
Product was shipped to the following sta…

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FDA Recall United States Terminated Historical recordClass I

The Mochi Ice Cream Company

Product
My Mochi Sorbet Peach Mango Sorbet; Keep Frozen; 6 pieces pe…
Reason
Frozen Peach Mango Sorbet contains undeclared allergen (egg)
Published
February 5, 2025
Distribution
Nationwide

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FDA Recall Completed Historical recordClass III

Venlafaxine Extended-Release Tablets, 150mg, Rx only, 90 Tablets, Manufactured by Appco Pharma. LLC, NDC 43598-943-90.

by Appco Pharma LLC

Reason
Failed Tablet/Capsule Specifications: Missing tab ID on either side of the tablet
Published
January 29, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass I

FOUZEE SugarLin HERBAL FORMULA capsules, 180 capsules per bottle, Sold and Distributed by Shoppers-Plaza, Hawthorne, CA 90250. Product of India. UPC 8 26656 69047 7

by SHOPPERS- PLAZA

Reason
Marketed without an Approved NDA/ANDA; FDA laboratory analysis confirmed product tainted with undeclared metformin and glyburide
Published
January 29, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

First Aid Beauty Ultra Repair Cream, colloidal oatmeal 0.5%, Coconut Vanilla, Net Wt. 396.8 g (14 OZ), DISTR. BY: First Aid Beauty LTD, Newton, MA, 02458, UPC 8 15517 02955 6

by First Aid Beauty Ltd

Reason
CGMP Deviations; product intended for quarantine was inadvertently distributed
Published
January 29, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Kissable Diabetics Foot Cream, NET WT 4 oz (113 g) per tube, Manufactured By: Brands International Corp., Newmarket, ON, L3X 2S2. UPC 6 72008 80925 3

by Brands International Corporation

Reason
CGMP Deviations: lack of adequate release testing.
Published
January 29, 2025
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Cardura XL (doxazosin) extended release tablets 4 mg, 30 -count bottle, Rx only, Distributed by Viatris Specialty LLC, Morgantown, WV 26505, NDC 58151-078-93

by Viatris Inc

Reason
Failed Impurities/Degradation Specifications: Out of specification results observed for the impurity compound B during stability testing.
Published
January 22, 2025
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Cardura XL (doxazosin) extended release tablets 8 mg, 30-count bottle, Rx only, Distributed by Viatris Specialty LLC, Morgantown, WV 26505, NDC 58151-079-93

by Viatris Inc

Reason
Failed Impurities/Degradation Specifications: Out of specification results observed for the impurity compound B during stability testing.
Published
January 22, 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.