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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.

37,115
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.

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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 II24,343
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 6,661–6,680 of 20,945 recalls

FDA Recall United States Terminated Historical recordClass II

NutraCap Labs LLC

Product
RAW VEGAN PROTEIN PEANUT BUTTER NET WEIGHT 2.04LBS (925 GRAM…
Reason
During an FDA investigation the firm was notified that the product contains undeclared coconut.
Published
January 19, 2022
Distribution
Product was shipped to the following sta…

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FDA Recall United States Terminated Historical recordClass I

NutraCap Labs LLC

Product
ETEDREAM ETEGROW ISO SNICKER DOODLE NET WEIGHT: 1950G (68.78…
Reason
During an FDA investigation the firm was notified of the product contains undeclared milk.
Published
January 19, 2022
Distribution
Product was shipped to the following sta…

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FDA Recall United States Terminated Historical recordClass I

NutraCap Labs LLC

Product
Boba Origin Brown-Sugar Milk Tea 100% WHEY PROTEIN ISOLATE 5…
Reason
During an FDA investigation the firm was notified that the product contains undeclared milk and soy.
Published
January 19, 2022
Distribution
Product was shipped to the following sta…

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FDA Recall United States Terminated Historical recordClass II

Local Fixe LLC

Product
Squid Ink- Fettucine is raw fresh pasta portioned into 4 oun…
Reason
Flour is declared but Wheat is not declared on label.
Published
January 19, 2022
Distribution
Distributed in OR only.

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FDA Recall United States Terminated Historical recordClass II

Local Fixe LLC

Product
Soup Noodles are raw pasta cut into assorted rectangle shape…
Reason
Flour is declared but Wheat is not declared on label.
Published
January 19, 2022
Distribution
Distributed in OR only.

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FDA Recall United States Terminated Historical recordClass II

Local Fixe LLC

Product
Dinner Rolls are shaped in rounds and sold frozen. Packaged…
Reason
Flour is declared but Wheat is not declared on label.
Published
January 19, 2022
Distribution
Distributed in OR only.

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FDA Recall United States Terminated Historical recordClass II

Local Fixe LLC

Product
Pie Dough are packaged two crusts per pack and sold frozen.…
Reason
Flour is declared but Wheat is not declared on label.
Published
January 19, 2022
Distribution
Distributed in OR only.

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FDA Recall United States Terminated Historical recordClass II

Local Fixe LLC

Product
Fresh Flour Tortillas are packaged in a clear Ziploc style p…
Reason
Flour is declared but Wheat is not declared on label.
Published
January 19, 2022
Distribution
Distributed in OR only.

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FDA Recall United States Terminated Historical recordClass I

DREAM POPS

Product
100% Plant-Based Dream Pops Birthday Cake Bites UPC 85409700…
Reason
Undeclared allergen; milk
Published
January 19, 2022
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

DREAM POPS

Product
100% Plant-Based Dream Pops Berry Dreams Bites UPC 854097008…
Reason
Undeclared allergen; milk
Published
January 19, 2022
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

DREAM POPS

Product
100% Plant-Based Dream Pops Vanilla Sky Bites UPC 8540970082…
Reason
Undeclared allergen; milk
Published
January 19, 2022
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Joseph Seviroli Inc.

Product
Aplenty Rotini with Plant based Bolognese Meal Kit 24oz
Reason
May contain undeclared milk
Published
January 19, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Pregabalin Capsules, 50 mg, 100 count bottle, Rx only, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, Manufactured by: Sun Pharmaceutical Industries Ltd., Survey No. 259/15 Dadra-396 191, (U.T. of D & NH), India, NDC 47335-687-88.

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason
Failed Tablet/Capsule Specifications: Out of Specification results for particle Size Distribution and Bulk Density of the Active Pharmaceutical Ingredient.
Published
January 12, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Cefixime Capsules, 400 mg, 50-count bottles, Rx only, Manufactured by: Alkem Laboratories Ltd., Mumbai, India, Distributed by: Ascend Laboratories, LLC, Parsippany, NJ, NDC 67877-584-50

by Ascend Laboratories, LLC

Reason
Failed impurities/degradation specifications
Published
January 12, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

GoodSense Aller.Ease, Fexofenadine hydrochloride 24 HR, 180 mg tablets, 30 count bottle, Made in the Czech Republic, Distributed by Perrigo Allergan MI., 49010, UPC 3 0113 0571 39 3; NDC 0113-0571-30,

by Perrigo Company PLC

Reason
Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Published
January 12, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

CVS Allergy Relief, Fexofenadine Hydrochloride Tablets, 180 mg Antihistamine, 24HR, 30 count bottle, NDC 69842-698-39, UPC 0 50428 62564 4

by Perrigo Company PLC

Reason
Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Published
January 12, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

KIRKLAND ALLER-FEX, Fexofenadine Hydrochloride Tablets, 180 mg/Antihistamine, 24HR, 180 count bottle, Made in the Czech Republic, Packaged by Perrigo 515 Eastern Ave., Allegan, MI 49010, For Costco Wholesale Corporation. P.O. Box 34535 Seattle, WA 98124-1535, NDC 63981-571-48, UPC 0 96619 98776 4

by Perrigo Company PLC

Reason
Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Published
January 12, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

amazon basic+care, Allergy Fexofenadine Hydrochloride Tablets, 60 mg/Antihistamine, 12HR, 100 count bottle, Made in the Czech Republic, Distributed by: Amazon.com services LLC 410 Terry Avenue N., Seattle WA 98109, NDC 72288-425-78 UPC 3 70030 14536 2

by Perrigo Company PLC

Reason
Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Published
January 12, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Wal-Fex Fexofenadine Hydrochloride tablets, 60mg/antihistamine, 12HR, 24 count bottle, Distributed by Walgreen Co. 200 Wilmot Rd Deerfield IL 60015, Made in the Czech Republic, NDC 0363-0903-62 UPC 3 11917 18625 2

by Perrigo Company PLC

Reason
Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Published
January 12, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Wal-Fex Fexofenadine Hydrochloride tablets, 180mg/antihistamine, 24HR, packaged as a) 5 count bottle, NDC 0363-0600-13,UPC 3 11917 12267 0, b)30 count bottle, NDC 0363-0600-39 UPC 3 11917 16172 3 c) 90 count bottle, NDC 0363-0600-75 UPC 3 11917 12271 7 ; Distributed by Walgreen Co. 200 Wilmot Rd Deerfield IL 60015, Made in the Czech Republic,

by Perrigo Company PLC

Reason
Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Published
January 12, 2022
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.