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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.

37,142
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,799
Class I recallsReasonable probability of serious health consequences
24,349
Class II recallsTemporary or medically reversible health consequences
2,891
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 II24,349
Class I9,799
Class III2,891
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,349
Class I9,799
Class III2,891
Not Yet Classified1

Showing 12,161–12,180 of 21,635 recalls

FDA Recall Terminated Historical recordClass III

Amlodipine and Olmesartan Medoxomil Tablets, 5 mg/40 mg, Rx only, 30-count bottle, Distributed by: Aurobindo Pharma USA, Inc. 279 Princeton-Hightstown Road East Windsor, NJ 0852 Made in India, NDC 65862-855-30

by Aurobindo Pharma USA Inc.

Reason
Discoloration: This product is being recalled due to a confirmed pharmacist report that tablets from this lot were a pink color instead of cream (peach).
Published
December 12, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Ottogi America Inc

Product
Ottogi Jin Ramen Mild NET WT. 1lb 5.16oz, 600g (120gx5) 5P…
Reason
Undeclared allergen; egg.
Published
December 12, 2018
Distribution
U.S. distribution to the following: CA,…

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FDA Recall United States Terminated Historical recordClass I

Ottogi America Inc

Product
Ottogi Jin Ramen Spicy NET WT. 1lb 5.16oz, 600g (120gx5) 5…
Reason
Undeclared allergen; egg.
Published
December 12, 2018
Distribution
U.S. distribution to the following: CA,…

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FDA Recall United States Terminated Historical recordClass I

Agropur MSI Ingredients LLC

Product
Jay Robb Unflavored Egg White Protein, Net Weight 24 oz (1.5…
Reason
JayRobb Unflavored Egg White Protein Product is being recalled due to undeclared milk.
Published
December 12, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

First Source, LLC

Product
Chocolate and Nut Tray. The product comes in a four-quadrant…
Reason
Product contains undeclared pecans and cashews.
Published
December 12, 2018
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass II

Smartypants Vitamins

Product
Smartypants Kids Complete, Non GMO Multi and omega 3's vit…
Reason
Consumer complaints of finding foreign objects in bottles of gummy vitamins.
Published
December 12, 2018
Distribution
WA, IL, RI, MC, NJ, ID, IA, VA, NY, OH,…

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FDA Recall United States Terminated Historical recordClass II

Rich Products Corp

Product
VANILLA WHIPPED ICING ARTIFICALLY FLAVORED Product Number: 0…
Reason
Possible contamination with cleaning chemicals.
Published
December 12, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Clindamycin Phosphate Topical Solution USP, 1% (10 mg/mL clindamycin), 60 pledget applicators per jar, Rx only. Manufactured by Ei LLC 2865 N. Cannon Blvd. Kannapolis, NC 18083. NDC# 61748-0201-60

by Akorn, Inc.

Reason
Failed Impurities/Degradation Specifications; out of specification results observed for other individual impurities
Published
December 5, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Quetiapine Tablets USP 400 mg, 100 tablet bottles, Rx Only, Manufactured by: Alkem Laboratories Ltd., Mumbai - 400 013, India. Distributed by: Ascend Laboratories, LLC Parsippany, NJ 07054 --- NDC 67877-248-01, UPC code: 3 67877-248-01 1

by Ascend Laboratories LLC

Reason
Presence of Foreign Substance; metal shard found in tablet
Published
December 5, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Chukar Cherry Company

Product
Organic Ultra Dark Orange Chocolate Tart Cherries, Chukar Ch…
Reason
Product contains unintentional presence of milk and therefore milk was not listed on the label as an ingredient.
Published
December 5, 2018
Distribution
Distributed in AK, AZ, CA, CO, MD, ME, M…

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FDA Recall United States Terminated Historical recordClass I

Chukar Cherry Company

Product
Organic Ultra Dark Vanilla Chocolate Rainier Cherries, Chuka…
Reason
Product contains unintentional presence of milk and therefore milk was not listed on the label as an ingredient.
Published
December 5, 2018
Distribution
Distributed in AK, AZ, CA, CO, MD, ME, M…

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FDA Recall United States Terminated Historical recordClass I

Chukar Cherry Company

Product
Ultra Dark Chocolate Cocoa Pecans, Chukar Cherries brand, pa…
Reason
Product contains unintentional presence of milk and therefore milk was not listed on the label as an ingredient.
Published
December 5, 2018
Distribution
Distributed in AK, AZ, CA, CO, MD, ME, M…

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FDA Recall United States Terminated Historical recordClass I

Chukar Cherry Company

Product
Ultra Dark Chocolate Black Forest Cherries, Chukar Cherries…
Reason
Product contains unintentional presence of milk and therefore milk was not listed on the label as an ingredient.
Published
December 5, 2018
Distribution
Distributed in AK, AZ, CA, CO, MD, ME, M…

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FDA Recall United States Terminated Historical recordClass I

Chukar Cherry Company

Product
Ultra Dark Chocolate Amaretto Rainier Cherries, Chukar Cherr…
Reason
Product contains unintentional presence of milk and therefore milk was not listed on the label as an ingredient.
Published
December 5, 2018
Distribution
Distributed in AK, AZ, CA, CO, MD, ME, M…

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FDA Recall United States Terminated Historical recordClass II

ConAgra Foods, INc.

Product
Duncan Hines Signature Confetti Cake cake mix 15.25oz.…
Reason
positive finding of Salmonella in a retail sample
Published
December 5, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

ConAgra Foods, INc.

Product
Duncan Hines Classic Butter Golden cake mix 15.25oz. 12…
Reason
positive finding of Salmonella in a retail sample
Published
December 5, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

ConAgra Foods, INc.

Product
Duncan Hines Classic Classic Yellow cake mix 15.25oz. 1…
Reason
positive finding of Salmonella in a retail sample
Published
December 5, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

ConAgra Foods, INc.

Product
Duncan Hines Classic Classic White cake mix 15.25oz. 12…
Reason
positive finding of Salmonella in a retail sample
Published
December 5, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Chicago Importing Co

Product
Finax Muesli with 45% Fruit; 22.9-oz.; Heat sealed plastic…
Reason
The product's ingredients statement does not indicate presence of coconut
Published
December 5, 2018
Distribution
AZ CA FL IL MA MD MI MN NJ NY…

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FDA Recall Terminated Historical recordClass II

Clopidogrel Tablets, USP, 300 mg, 30 (5 x 6 unit-dose) count blister pack, Rx only, Manufactured by Dr. Reddy's Laboratories Limited, Srikakulam - 532 409, India, NDC 55111-671-31

by Dr. Reddy's Laboratories, Inc.

Reason
Failed Dissolution Specification: Out-of-Specification results were observed for dissolution at 18th month stability testing.
Published
November 28, 2018
Distribution
Nationwide

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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.