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Recall totals

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

37,143
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 13,741–13,760 of 19,943 recalls

FDA Recall Terminated Historical recordClass II

LATANOPROST OPHTHALMIC SOLUTION, 0.005%, 125 ug/2.5 mL, packaged in 2.5 mL bottle, Rx only, Manufactured for: Akorn, Inc., Lake Forest, IL 60045, NDC 17478-625-12

by Akorn, Inc.

Reason
Lack of assurance of sterility: product was found to be empty, under-filled, or leaking.
Published
April 19, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Levonorgestrel Non-Micronized, USP, Bulk, Rx only, For Prescription Compounding, Manufactured by Qinhuangdao Zizhu Pharmaceutical Co., Ltd., Qinhuangdao 066004, China (NDC 44132-012-01),

by Qinhuangdao Zizhu Pharmaceutical, Co.

Reason
cGMP Deviations; lack of quality assurance.
Published
April 19, 2017
Distribution
Product distributed to NY, TX, SC, CO, M…

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FDA Recall Terminated Historical recordClass II

Ethinyl Estradiol Micronized, USP, Bulk, Rx only, For Prescription Compounding, Manufactured by Qinhuangdao Zizhu Pharmaceutical Co., Ltd, Qinhuangdao 066004, China (NDC 44132-002-05)

by Qinhuangdao Zizhu Pharmaceutical, Co.

Reason
cGMP Deviations; lack of quality assurance.
Published
April 19, 2017
Distribution
Product distributed to NY, TX, SC, CO, M…

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FDA Recall Terminated Historical recordClass II

Testosterone Micronized, Bulk, Rx only, For Prescription Compounding, Manufactured by Qinhuangdao Zizhu Pharmaceutical Co., Ltd., Qinhuangdao 066004, China (NDC 44132-006-06)

by Qinhuangdao Zizhu Pharmaceutical, Co.

Reason
cGMP Deviations; lack of quality assurance.
Published
April 19, 2017
Distribution
Product distributed to NY, TX, SC, CO, M…

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FDA Recall Terminated Historical recordClass II

Estrone Micronized, USP, Bulk, Rx only, For Prescription Compounding, Manufactured by Qinhuangdao Zizhu Pharmaceutical Co., Ltd., Qinhuangdao 066004, China (NDC 44132-003-04) (NDC 44132-003-02)(NDC 44132-003-06)

by Qinhuangdao Zizhu Pharmaceutical, Co.

Reason
cGMP Deviations; lack of quality assurance.
Published
April 19, 2017
Distribution
Product distributed to NY, TX, SC, CO, M…

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FDA Recall Terminated Historical recordClass II

Estriol Micronized, USP, Bulk, Rx only, For Prescription Compounding, Manufactured by Qinhuangdao Zizhu Pharmaceutical Co., Ltd, Qinhuangdao 066004, China 44132-007-06

by Qinhuangdao Zizhu Pharmaceutical, Co.

Reason
cGMP Deviations; lack of quality assurance.
Published
April 19, 2017
Distribution
Product distributed to NY, TX, SC, CO, M…

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FDA Recall Terminated Historical recordClass II

Estradiol Non-Micronized, USP, Bulk, Rx only, For Prescription Compounding, Manufactured by Qinhuangdao Zizhu Pharmaceutical Co., Ltd, Qinhuangdao 066004, China

by Qinhuangdao Zizhu Pharmaceutical, Co.

Reason
cGMP Deviations; lack of quality assurance.
Published
April 19, 2017
Distribution
Product distributed to NY, TX, SC, CO, M…

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FDA Recall Terminated Historical recordClass II

Estradiol Micronized Bulk, Rx only, For Prescription Compounding, Manufactured by Qinhuangdao Zizhu Pharmaceutical Co., Ltd, Qinhuangdao 066004, China (NDC 44132-001-01) (44132-001-06)

by Qinhuangdao Zizhu Pharmaceutical, Co.

Reason
cGMP Deviations; lack of quality assurance.
Published
April 19, 2017
Distribution
Product distributed to NY, TX, SC, CO, M…

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FDA Recall Terminated Historical recordClass III

Fluocinolone Acetonide Topical Solution USP 0.01% For Topical Use Only, Not for Ophthalmic Use, 60 mL bottle, Rx Only, Manufactured for Gavis Pharmaceuticals, LLC, Somerset NJ 08873, Manufactured by Novel Laboratories, Inc. Somerset, NJ 08873, NDC 43386-069-60

by Novel Laboratories, Inc.

Reason
Chemical Contamination
Published
April 19, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Penicillin V Potassium Tablets, USP 500 mg (800,000 units) 1000 count bottles, Rx Only, Distributed by: Citron Pharma LLC, East Brunswick, NJ --- NDC 57237-041-99

by Citron Pharma Llc

Reason
Presence of Foreign Tablet/Capsule; Amoxicillin 500 mg was found in bottles of Penicillin V potassium 500 mg
Published
April 19, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Gerber Products Company dba Nestle Infant Nutrition

Product
Gerber¿ Pasta Pick-Ups Cheese Ravioli Net Wt 6 oz (170g)…
Reason
Gerber Products Company is recalling Cheese Ravioli Gerber¿ Pasta Pick-Ups¿ because the egg allergen is missing from the "Contains" statement.
Published
April 19, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

The SoyNut Butter Company

Product
B'Gan Quality Product, SoyNut Butter, Creamy; Dist. By: S. B…
Reason
Potential contamination of product with E. coli O157.
Published
April 19, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

The SoyNut Butter Company

Product
I.M. Healthy Blueberry Granola; Peanut Free; The SoyNut butt…
Reason
Potential contamination of product with E. coli O157.
Published
April 19, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

The SoyNut Butter Company

Product
I.M. Healthy Apple Granola; Peanut Free; The SoyNut butter C…
Reason
Potential contamination of product with E. coli O157.
Published
April 19, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

The SoyNut Butter Company

Product
I.M. Healthy, Chocolate SoyNut Butter; Peanut Free; The SoyN…
Reason
Potential contamination of product with E. coli O157.
Published
April 19, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

The SoyNut Butter Company

Product
I.M. Healthy, Honey Creamy SoyNut Butter; Peanut Free; The S…
Reason
Potential contamination of product with E. coli O157.
Published
April 19, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

The SoyNut Butter Company

Product
I.M. Healthy, Unsweetened SoyNut Butter; Peanut Free; The So…
Reason
Potential contamination of product with E. coli O157.
Published
April 19, 2017
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

The SoyNut Butter Company

Product
I.M. Healthy, Creamy SoyNut Butter; Peanut Free; The SoyNut…
Reason
Potential contamination of product with E. coli O157.
Published
April 19, 2017
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

NONNA FOODS

Product
LIDIA'S MARINARA, NET WT 25 oz (708g), UPC 897712001018 ---…
Reason
The product may contain undeclared milk due potential product mix-up.
Published
April 19, 2017
Distribution
New York, New Jersey, Connecticut, Rhode…

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FDA Recall United States Terminated Historical recordClass I

The SoyNut Butter Company

Product
Dixie Diners' Club Carb Not Beanit Butter, 15oz., Dixie USA,…
Reason
Potential contamination of product with E. coli O157.
Published
April 19, 2017
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.