Skip to main content

Data Explorer

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.

Filters
Recall details
Location
Date range
Sort results
Clear filters
Metric
View
Recalls announced by month (Year to date)

A chart of recalls grouped by month.

Download CSV

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 15,201–15,220 of 23,259 recalls

FDA Recall United States Terminated Historical recordClass I

Silver Spring Foods, Inc.

Product
waterfront Bistro Tatar Sauce, Net Wt 9 oz. (255g), UPC 2113…
Reason
Silver Spring is recalling Waterfront Bistro Tartar Sauce because an incorrect back label does not identify egg.
Published
October 18, 2017
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Apple King, LLC

Product
Fuji apples, Nature's Delight brand, packaged in tray pack b…
Reason
Fuji apples are recalled because Thiabendazole was detected at 6.9 ppm.
Published
October 18, 2017
Distribution
distributed in AL, AZ, CA, CO, FL, GA, H…

View recall →

FDA Recall Terminated Historical recordClass II

Choice Antibacterial Hand Soap, (ethyl alcohol 61%) 800 ml/ 27 fl oz, Universal Valve, Inopak LTD, Ringwood, NJ

by Inopak Ltd

Reason
GMP Deviations; potential bacterial contamination may have been introduced to products through a contaminated diaphragm pump.
Published
October 11, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Mild Healthcare Antibacterial Hand Soap, 6% P.C.M.X., 1000 mL and 2000 mL Disc Pump, 800 mL Universal Valve, and 1 gallon bottles, Inopak. Ltd, Ringwood, NJ 07456

by Inopak Ltd

Reason
GMP Deviations; potential bacterial contamination may have been introduced to products through a contaminated diaphragm pump.
Published
October 11, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Option Systems Antibacterial Foaming Hand Wash, 0.3% P.C.M.X., 8 fl oz and 18 fl oz. bottles and 500, mL 800 mL, and 1000 mL pouches, ALSO labeled as STYLE Antibacterial Hand Soap, Inopak Ltd Ringwood, NJ --- NDC 5031-431-02

by Inopak Ltd

Reason
GMP Deviations; potential bacterial contamination may have been introduced to products through a contaminated diaphragm pump
Published
October 11, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Deferoxamine Mesylate for injection, USP, Single-use Vial, 500 mg/vial, 10 mL vial. Intravenous, Intramuscular, Subcutaneous Use, Rx Only, Hospira, Inc., Lake Forest IL USA, NDC 0406-2336-10.

by Pfizer Inc.

Reason
CGMP Deviations: Firm failed to control impurity for color change at the API stage.
Published
October 11, 2017
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

Cargill Cocoa and Chocolate, Inc.

Product
Shoprite Real Semi-Sweet Chocolate Chips, Net Wt. 24 oz., UP…
Reason
Cargill Cocoa & Chocolate is recalling Shoprite Real Semi-Sweet Chocolate Chips due to undeclared milk.
Published
October 11, 2017
Distribution
Shop Rite and The Fresh Grocer and other…

View recall →

FDA Recall United States Terminated Historical recordClass I

Garden Of Life, LLC

Product
Garden of Life, Baby Organic Liquid probiotic formula, 56 ml…
Reason
The product may pose a choking hazard to newborns due to the thickness of the liquid.
Published
October 11, 2017
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Grand Supercenter Inc.

Product
HAIOREUM, RICE PANCAKE, KOREAN STYLE SNACK 5.29 OZ (150 G),…
Reason
The firm, Grand Supercenter Inc., was notified by USFDA NY District Office that they received a report from a consumer in which there was an allergy reaction after the person consumed Haioreum Rice Pop Snack. The firm Grand Supercenter Inc. has decided to recall the product involved in this incident due to Undeclared Wheat allergen.
Published
October 11, 2017
Distribution
Products are mostly distributed to store…

View recall →

FDA Recall United States Terminated Historical recordClass II

Grand Supercenter Inc.

Product
HAIOREUM, RICE PANCAKE, KOREAN STYLE SNACK 5.29 OZ (150 G),…
Reason
The firm, Grand Supercenter Inc., was notified by USFDA NY District Office that they received a report from a consumer in which there was an allergy reaction after the person consumed Haioreum Rice Pop Snack. The firm Grand Supercenter Inc. has decided to recall the product involved in this incident due to Undeclared Wheat allergen.
Published
October 11, 2017
Distribution
Products are mostly distributed to store…

View recall →

FDA Recall United States Terminated Historical recordClass II

Grand Supercenter Inc.

Product
HAIOREUM, RICE PANCAKE, KOREAN STYLE SNACK 5.29 OZ (150 G),…
Reason
The firm, Grand Supercenter Inc., was notified by USFDA NY District Office that they received a report from a consumer in which there was an allergy reaction after the person consumed Haioreum Rice Pop Snack. The firm Grand Supercenter Inc. has decided to recall the product involved in this incident due to Undeclared Wheat allergen.
Published
October 11, 2017
Distribution
Products are mostly distributed to store…

View recall →

FDA Recall United States Terminated Historical recordClass II

Grand Supercenter Inc.

Product
HAIOREUM, RICE POP SNACK, KOREAN STYLE SNACK 0.41 LBS (190 G…
Reason
The firm, Grand Supercenter Inc., was notified by USFDA NY District Office that they received a report from a consumer in which there was an allergy reaction after the person consumed Haioreum Rice Pop Snack. The firm Grand Supercenter Inc. has decided to recall the product involved in this incident due to Undeclared Wheat allergen.
Published
October 11, 2017
Distribution
Products are mostly distributed to store…

View recall →

FDA Recall United States Terminated Historical recordClass II

Pro Bioteks Laboratories

Product
Bio35, Vitamin-Mineral Omega Oils Trace Minerals Dietary Sup…
Reason
Bio-35 has undeclared soy lecithin.
Published
October 11, 2017
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

KIND LLC

Product
KIND Dark Chocolate Nuts and Sea Salt Bar-containing 12 /1.…
Reason
Outer box fails to declare the allergen walnuts, the individual bar is properly labeled
Published
October 11, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Ampicillin for Injection, USP, 500 mg per vial, single vial (NDC 0781-3407-78) packaged in 10-count shrink wrap packs (NDC 0781-3407-95), Rx only, Manufactured in Austria by Sandoz GmbH or Sandoz Inc., Princeton, NJ 08540.

by Sandoz Inc

Reason
Labeling: Missing Label: customer complaint that some vials of ampicillin within the shrink wrap pack are missing labels.
Published
October 4, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Acarbose Tablets, 25 mg, 100-count bottle, Rx only, Manufactured by: Arrow Pharm (Malta) Ltd., Birzebbugia BBG3000, Malta; Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054; NDC 16252-523-01.

by Teva Pharmaceuticals USA

Reason
Labeling: Incorrect or Missing Lot and/or Exp Date: An incorrect expiration date of July 2018 is printed on the product labeling rather than the correct expiration date of July 2017.
Published
October 4, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Sterile Water for Injection, USP Single Dose 100 mL vials, Rx only, Manufactured by Hospira, Inc., Lake Forest, IL 60045 USA for Genentech, Inc., South San Francisco, CA 94080-4990. NDC 50242-901-24

by Pfizer Inc.

Reason
Non-Sterility: cracked or chipped glass at the neck of Sterile Water for Injection vials.
Published
October 4, 2017
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

House Of Thaller Inc

Product
Marketside CLASSIC HUMMUS WITH PINE NUTS NET WT. 10 oz (283g…
Reason
The firm was notified by their ingredient supplier that the pine nuts may be contaminated with Listeria monocytogenes.
Published
October 4, 2017
Distribution
Product was shipped to the following sta…

View recall →

FDA Recall United States Terminated Historical recordClass I

Treehouse Foods

Product
Wegmans Dark Chocolate Cherry Cashew chewy granola bars, 12-…
Reason
Wegmans Dark Chocolate Cherry Cashew Bars are recalled because there may be a higher concentration of Vitamin A, than what is declared
Published
October 4, 2017
Distribution
NY

View recall →

FDA Recall United States Terminated Historical recordClass I

House Of Thaller Inc

Product
LANTANA White Bean HUMMUS NET WT. 10 oz (283g)
Reason
The firm was notified by their ingredient supplier that the pine nuts may be contaminated with Listeria monocytogenes.
Published
October 4, 2017
Distribution
Product was shipped to the following sta…

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.