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Recall totals

All FDA and USDA recalls in Public Health Trace, June 2012 to November 2026.

37,449

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,872

Class I recallsReasonable probability of serious health consequences

24,509

Class II recallsTemporary or medically reversible health consequences

2,932

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 2,096 recalls

Newest recallhttps://www.fsis.usda.gov/recalls-alerts/fsis-issues-public-health-alert-meat-and-poultry-products-due-misbranding-andPublished November 6, 2026

Most affected stateHawaii 200 recalls mention this state

State: MD ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated November 7, 2026 ET

Summary (Year to date)

1,956 recalls have been announced year to date.
Oct 2026 was 4% higher than the previous complete period (Sep 2026: 209).
The highest complete period was Jun 2026 (300).
Nov 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,509
Class I	9,872
Class III	2,932
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,509
Class I	9,872
Class III	2,932
Not Yet Classified	2

FDA Recall United States TerminatedTerminated: May 21, 2024Historical recordClass I

NutraCap Labs LLC

Product: Alpha Woman Original Capsules, 60ct Bottle, UPC CODE 11883 6…
Reason: During an FDA investigation the firm was notified that 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 TerminatedTerminated: May 21, 2024Historical recordClass I

NutraCap Labs LLC

Product: AIOS Synergy for Women Capsules 120ct Bottle
Reason: During an FDA investigation the firm was notified that 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 TerminatedTerminated: May 21, 2024Historical recordClass I

NutraCap Labs LLC

Product: AIOS Synergy for Men Capsules 120ct Bottle
Reason: During an FDA investigation the firm was notified that 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 TerminatedTerminated: May 21, 2024Historical recordClass I

NutraCap Labs LLC

Product: Adrenalyne Razzled Up Blue Raspberry 25oz jar
Reason: During an FDA investigation the firm was notified that the product contains undeclared shellfish.
Published: January 19, 2022
Distribution: Product was shipped to the following sta…

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FDA Recall United States TerminatedTerminated: May 21, 2024Historical recordClass I

NutraCap Labs LLC

Product: Adrenalyne Crimson Crush Fruit Punch 25oz jar
Reason: During an FDA investigation the firm was notified that the product contains undeclared shellfish.
Published: January 19, 2022
Distribution: Product was shipped to the following sta…

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FDA Recall United States TerminatedTerminated: May 21, 2024Historical recordClass I

NutraCap Labs LLC

Product: Vital Force PUREISO 100% WHEY PROTEIN ISOLATE CREAMY PEANUT…
Reason: During an FDA investigation the firm was notified that 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 TerminatedTerminated: May 21, 2024Historical recordClass I

NutraCap Labs LLC

Product: STEEL VEG-PRO COOKIES & CREME 100% PURE VEGAN PROTEIN NET WT…
Reason: During an FDA investigation the firm was notified that the product contains undeclared wheat.
Published: January 19, 2022
Distribution: Product was shipped to the following sta…

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FDA Recall United States TerminatedTerminated: May 21, 2024Historical 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 TerminatedTerminated: May 21, 2024Historical 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 TerminatedTerminated: May 21, 2024Historical 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 TerminatedTerminated: July 8, 2022Historical recordClass II

Lidl US Operations, LLC

Product: Vemondo Vegan Coconut & Cocoa Non-Dairy Dessert Cones 4-3.7…
Reason: Undeclared milk allergen
Published: January 19, 2022
Distribution: Distributed to retail stores in MD, VA,…

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FDA Recall United States TerminatedTerminated: February 16, 2022Historical 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 TerminatedTerminated: February 16, 2022Historical 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 TerminatedTerminated: February 16, 2022Historical 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 TerminatedTerminated: October 27, 2022Historical 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 TerminatedTerminated: April 6, 2023Historical 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 TerminatedTerminated: April 13, 2023Historical 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 TerminatedTerminated: November 8, 2022Historical 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 TerminatedTerminated: November 8, 2022Historical 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 TerminatedTerminated: November 8, 2022Historical 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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Data last updated: November 7, 2026 ET

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.