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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 11,781–11,800 of 19,943 recalls

FDA Recall Terminated Historical recordClass II

RANITIDINE Tablets, USP 150 mg UD 100 tablets (10x10), RX Only, Manufactured by: Amneal Pharmaceuticals, Hauppauge, NY 11788, NDC 63739-489-10

by Mckesson Packaging Services

Reason
Failed Stability Specifications
Published
March 14, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Lynparza (olaparib) capsules 50 mg, 112 count bottles, Rx only, Manufactured for: Astra Zeneca Pharmaceuticals LP Wilmington, DE 19850 by: Patheon Pharmaceuticals, Inc. Cincinnati OH 45237 Product of Switzerland NDC 0310-0657-58

by AstraZeneca Pharmaceuticals LP

Reason
Failed Impurities/Degradation Specifications; elevated levels of quality attribute Form L (polymorph).
Published
March 14, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Methylphenidate Hydrochloride Extended-release Tablets, USP, 36 mg, 100-count bottle, Rx only, Trigen Laboratories, LLC Bridgewater, NJ 08807. NDC 13811-708-10

by Osmotica Pharmaceutical Corp

Reason
Subpotent Drug:100-count product bottle labeled as Methylphenidate HCL ER Tablets 36 mg found to contain 1 27 mg Methylphenidate HCL ER Tablet.
Published
March 14, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Atropine Sulfate Ophthalmic 1% Solution, USP, 5mL per bottle, Sterile, Rx Only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. NDC: 17478-215-05

by Akorn, Inc.

Reason
Failed Stability Specification: OOS low viscosity results discovered during retain testing.
Published
March 14, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Labetalol Hydrochloride Injection, USP, 100 mg/ 20 mL (5 mg/mL), 20 mL Multidose Vial, Rx only, labeled as a) Hospira, Inc., Lake Forest, IL 60045, NDC 0409-2267-20; and b) NOVAPLUS, Manufactured by Hospira, Inc., Lake Forest, IL 60045, NDC 0409-2267-25.

by Hospira Inc. A Pfizer Company

Reason
Defective Container: Cracked glass at the rim surface of glass vials, covered by the stopper and crimp seal.
Published
March 14, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass III

Springside Cheese Corp

Product
Springside Monterey Jack Caribbean Red Hot Cheese Packaged i…
Reason
Various cheeses are being recalled because they may have been made with milk that was held for 13.8 seconds during pasteurization.
Published
March 14, 2018
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass III

Springside Cheese Corp

Product
Springside Monterey Jack Chicken Soup Cheese Packaged in the…
Reason
Various cheeses are being recalled because they may have been made with milk that was held for 13.8 seconds during pasteurization.
Published
March 14, 2018
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass III

Springside Cheese Corp

Product
Springside Monterey Jack Chipotle Cheese Packaged in the fol…
Reason
Various cheeses are being recalled because they may have been made with milk that was held for 13.8 seconds during pasteurization.
Published
March 14, 2018
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass III

Springside Cheese Corp

Product
Springside Monterey Jack Cheese Packaged in the following si…
Reason
Various cheeses are being recalled because they may have been made with milk that was held for 13.8 seconds during pasteurization.
Published
March 14, 2018
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass III

Springside Cheese Corp

Product
Springside Monterey Jack Habanero Cheese Packaged in the fol…
Reason
Various cheeses are being recalled because they may have been made with milk that was held for 13.8 seconds during pasteurization.
Published
March 14, 2018
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass III

Springside Cheese Corp

Product
Springside Monterey Jack Morel & Leek Cheese Packaged in the…
Reason
Various cheeses are being recalled because they may have been made with milk that was held for 13.8 seconds during pasteurization.
Published
March 14, 2018
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass III

Springside Cheese Corp

Product
Springside Monterey Jack Onion & Chives Cheese Net Wt. 1 lb.
Reason
Various cheeses are being recalled because they may have been made with milk that was held for 13.8 seconds during pasteurization.
Published
March 14, 2018
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass III

Springside Cheese Corp

Product
Springside Monterey Jack Ghost Pepper Cheese packaged in the…
Reason
Various cheeses are being recalled because they may have been made with milk that was held for 13.8 seconds during pasteurization.
Published
March 14, 2018
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass III

Springside Cheese Corp

Product
Springside Monterey Jack Pueblo Cheese packaged in the follo…
Reason
Various cheeses are being recalled because they may have been made with milk that was held for 13.8 seconds during pasteurization.
Published
March 14, 2018
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass III

Springside Cheese Corp

Product
Springside Monterey Jack Jalapeno Cheese packaged in the fol…
Reason
Various cheeses are being recalled because they may have been made with milk that was held for 13.8 seconds during pasteurization.
Published
March 14, 2018
Distribution
Multiple states

View recall →

FDA Recall United States Terminated Historical recordClass III

Springside Cheese Corp

Product
Springside Monterey Jack Tomato Basil Cheese, Net Wt. 40 lb…
Reason
Various cheeses are being recalled because they may have been made with milk that was held for 13.8 seconds during pasteurization.
Published
March 14, 2018
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass III

Springside Cheese Corp

Product
Springside Monterey Jack Garden Vegetable Cheese, 40 lbs.
Reason
Various cheeses are being recalled because they may have been made with milk that was held for 13.8 seconds during pasteurization.
Published
March 14, 2018
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

Lotte International America Corp.

Product
Lotte Kancho Choco-Biscuit; Sold as Lotte Kancho - 42 g…
Reason
Firm was notified by customer of peanut allergen found in the product during product sampling and testing in Kancho Choco Biscuits.
Published
March 14, 2018
Distribution
Nationwide

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FDA Recall United States Ongoing Historical recordClass II

Snyder's-Lance Inc.

Product
Emerald brand Glazed Walnuts; Net WT. 6.5 OZ; Re-sealable po…
Reason
Snyder's Lance is voluntarily recalling 6.5 oz. Emerald brand walnuts due to the presence of undeclared peanuts, almonds, cashews, and pecans.
Published
March 14, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Vitalab Co Inc

Product
Product packaged in the following ways A) Sonne's, No. 17, N…
Reason
The firm's vitamin C dietary supplement contains lactose, a milk-derived ingredient, but fails to declare the major food allergen "milk" on the label.
Published
March 14, 2018
Distribution
Product distributed to consumers, distri…

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.