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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 October 2026.

37,205
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,841
Class I recallsReasonable probability of serious health consequences
24,366
Class II recallsTemporary or medically reversible health consequences
2,892
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 2,073 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)

  • 1,714 recalls have been announced year to date.
  • Sep 2026 was 3% higher than the previous complete period (Aug 2026: 182).
  • The highest complete period was Jun 2026 (297).
  • Oct 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 II24,366
Class I9,841
Class III2,892
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,366
Class I9,841
Class III2,892
Not Yet Classified2

Showing 14,661–14,680 of 23,259 recalls

FDA Recall Terminated Historical recordClass II

Relumins Advanced Glutathione kits, 900 mg vials, 1500 mg vials and 3000 mg vials

by Flawless Beauty LLC

Reason
Marketed Without An Approved NDA/ANDA: Flawless Beauty, LLC is voluntarily recalling all lots of different products sold individually or as part of multi-unit kits in accordance with Consent Decree of Permanent Injunction ordered by the United States District Court due to misbranding and unapproved new drugs pursuant to the FD&C Act.
Published
February 14, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

All sterile drug preparations remaining within expiry prepared from Sufentanil Citrate Base Solution dispensed between October 16, 2017 and November 17, 2017, Compounded by Intrathecal Compounding Specialists, Scott, LA 70583.

by Intrathecal Compounding Specialist, LLC

Reason
Lack of sterility assurance.
Published
February 14, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

All sterile drug preparations remaining within expiry prepared from Morphine Sulfate PF Base Solution dispensed between October 16, 2017 and November 17, 2017, Compounded by Intrathecal Compounding Specialists, Scott, LA 70583.

by Intrathecal Compounding Specialist, LLC

Reason
Lack of sterility assurance.
Published
February 14, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

All sterile drug preparations remaining within expiry prepared from Hydromorphone Base Solution dispensed between October 16, 2017 and November 17, 2017, Compounded by Intrathecal Compounding Specialists, Scott, LA 70583.

by Intrathecal Compounding Specialist, LLC

Reason
Lack of sterility assurance.
Published
February 14, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

All sterile drug preparations remaining within expiry prepared from Fentanyl Citrate Base Solution dispensed between October 16, 2017 and November 17, 2017 Compounded by Intrathecal Compounding Specialists, Scott, LA 70583.

by Intrathecal Compounding Specialist, LLC

Reason
Lack of sterility assurance.
Published
February 14, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Ciclopirox Olamine Cream USP, 0.77%, packaged in a) 15 g tubes (NDC 0713-0638-15); b) 30 g tubes (NDC 0713-0638-31); and c) 90 g tubes (NDC 0713-0638-18), Rx Only, Manufactured by: G&W Laboratories, Inc., South Plainfield, NJ 07080.

by G & W Laboratories, Inc.

Reason
Discoloration: Product is supposed to be a white to off white homogenous cream and may have intermittent yellow discoloration.
Published
February 14, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Panera, LLC

Product
Reduced-Fat Wild Blueberry Cream Cheese, 2 oz. and 8 oz.
Reason
Product may be contaminated with Listeria monocytogenes.
Published
February 14, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Panera, LLC

Product
Panera Reduced-Fat Honey Walnut Cream Cheese, 2 oz. and 8 oz…
Reason
Product may be contaminated with Listeria monocytogenes.
Published
February 14, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Panera, LLC

Product
Panera Chive&Onion Reduced Fat Cream Cheese Spread, 2 oz. an…
Reason
Product may be contaminated with Listeria monocytogenes.
Published
February 14, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Despana Brand Foods

Product
DON BOCARTE ARTE EN EL PALADAR MIGAS BONITO DEL NORTE PESCA…
Reason
Product may have elevated levels of Scombrotoxin (histamine).
Published
February 14, 2018
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass II

Ventura Foods Llc

Product
SunGlow, European Style Butter Blend Margarine, packaged in…
Reason
SunGlow contains undeclared soy lecithin.
Published
February 14, 2018
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass II

Ventura Foods Llc

Product
SunGlow, Unsalted European Style Butter Blend Margarine (169…
Reason
SunGlow contains undeclared soy lecithin.
Published
February 14, 2018
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

Mountain Rose Inc

Product
Prickly Ash Bark Powder Herbal Supplement, packaged in food…
Reason
Prickly Ash Bark Powder is recalled due to a potential contamination with Salmonella.
Published
February 14, 2018
Distribution
distributed in AK, AR, AZ, CA, CO , FL,…

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FDA Recall United States Terminated Historical recordClass II

Olde Thompson, Inc.

Product
Olde Thompson Sweet & Smoky BBQ Grinder NET WT. 6.7 oz. (1…
Reason
The seasoning mix Nutrition label states that the sodium content is 0 mg, when it actually contains 350 mg of salt per serving.
Published
February 14, 2018
Distribution
TX, AZ, VT, RI - Samples to CA, MN, NC,…

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FDA Recall United States Terminated Historical recordClass II

Simply Delicious, Inc. dba Bobo's Oat Bars

Product
Bobo's Coconut Oat Bar 3oz. Packaged in overwrap film per…
Reason
Bobo's recalled Coconut 3oz Bar due to mold.
Published
February 14, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Panera, LLC

Product
Panera Reduced-Fat Plain Cream Cheese, 2 oz. and 8 oz.
Reason
Product may be contaminated with Listeria monocytogenes.
Published
February 14, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Panera, LLC

Product
Panera Plain Cream Cheese, 2 oz. and 8 oz.
Reason
Product may be contaminated with Listeria monocytogenes.
Published
February 14, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

J F C International Inc

Product
Daisho Kimchi Hot Pot Soup Base; 1.60 lb pouch (10 units per…
Reason
Daisho Kimchi Hot Pot Soup base contains undeclared fish - shrimp and crab.
Published
February 14, 2018
Distribution
CA, NV, WA, OR, UT, AK, AZ, TX, OK, OH,…

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FDA Recall United States Terminated Historical recordClass I

Bulletproof 360 Inc

Product
Bulletproof Unflavored Collagen Protein High Performance Bui…
Reason
Bulletproof Collagen Protein is recalled due to undeclared milk. The actual product inside the package is whey (milk) protein but mis-labeled as collagen protein.
Published
February 14, 2018
Distribution
distributed in CA, CO, CT, FL, GA, IA, I…

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FDA Recall United States Terminated Historical recordClass II

CHOBANI

Product
Chobani Flip Key Lime Crumble - Key Lime Low-Fat Greek Yogur…
Reason
Product is recalled because a statement on the overwrap label erroneously states "No Gluten" while the ingredients statement and the Contains statements on both the overwrap label and the flip label on each individual cup declare wheat.
Published
February 14, 2018
Distribution
distributed in AL, AR, AZ, CA, CO, CT,…

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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.