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.

37,327

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,859

Class I recallsReasonable probability of serious health consequences

24,440

Class II recallsTemporary or medically reversible health consequences

2,900

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 2,095 recalls

Newest recallhttps://www.fsis.usda.gov/recalls-alerts/imperio-distribution-llc-recalls-beef-jerky-products-produced-without-benefitPublished October 24, 2026

Most affected stateHawaii 200 recalls mention this state

State: IN ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated October 26, 2026 ET

Summary (Year to date)

1,739 recalls have been announced year to date.
Sep 2026 was 15% higher than the previous complete period (Aug 2026: 182).
The highest complete period was Jun 2026 (300).
Oct 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,440
Class I	9,859
Class III	2,900
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,440
Class I	9,859
Class III	2,900
Not Yet Classified	2

FDA Recall Ongoing2026 recordClass II

CUROSURF (poractant alfa), 240 mg, Intratracheal Suspension, 3L Single-dose-Vial, Rx only, Chiesi USA, Inc, Cary, NC 27518, NDC 10122-510-03.

by Chiesi USA, Inc.

Reason: Lack of Assurance of Sterility
Published: April 1, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass III

Gelatin Capsule Pack for use with the Sodium Iodide I-131 Kit (containing 5 empty capsules and 5 Dibasic Sodium Phosphate Capsules 300 mg, International Isotopes Inc., Idaho Falls, ID 83401. NDC: 69208-003-15; 69208-003-25; 69208-003-35

by Radnostix

Reason: Failed Tablet/Capsule Specifications
Published: April 1, 2026
Distribution: Nationwide

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FDA Recall United States Ongoing2026 recordClass I

Siluetaya, LLC

Product: SiluetaYa Mexican Tejocote Roots Supplement Pieces; 7g/bottl…
Reason: Product contains yellow oleander
Published: April 1, 2026
Distribution: Product was distributed directly to cons…

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FDA Recall United States TerminatedTerminated: April 28, 20262026 recordClass II

Albertsons Companies LLC

Product: Lucerne 2% Cottage Cheese 2% Milkfat Small Curd Vitamin A Ad…
Reason: Metal fragments. The potential foreign object is a hard, metal (stainless steel), curled spring. Dimensions of a similar spring measure 2.27mm in cross-sectional thickness and 25.38mm in coil width. Spring ends are not sharp but may be sharp if broken/ cut.
Published: April 1, 2026
Distribution: Distributed in AK, ID, CA, OR, and WA.

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FDA Recall United States Ongoing2026 recordClass II

South Florida Food, LLC

Product: Pan de Bono (Cheese Bread), 100 units per Paper Cardboard Bo…
Reason: Undeclared Soy.
Published: April 1, 2026
Distribution: Products distribute in FL

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FDA Recall United States TerminatedTerminated: July 27, 20262026 recordClass II

Rose and Shore, Inc.

Product: 14" Margarita Thin Crust Pizza; 8 units per case. Keep Froze…
Reason: potential foreign object (metal pieces) in ingredient (Tomatoes)
Published: April 1, 2026
Distribution: Product was distributed to a single reta…

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FDA Recall United States TerminatedTerminated: May 11, 20262026 recordClass II

Savannah Bee Company Inc.

Product: SAVANNAH BEE COMPANY HONEY BBQ SAUCE MUSTARD NET 16 FL OZ (4…
Reason: Undeclared Allergens: Soy & Wheat. The firm was notified by a customer that the product is labeled as Savannah Bee Company Honey BBQ Sauce "Mustard", but the product inside the bottle is a different flavor of BBQ sauce. After investigation, the firm determined that the product in the bottle is their Honey BBQ Sauce "Sweet". The BBQ sauce "Sweet" contains wheat and soy which is not listed on the BBQ Sauce "Mustard" label.
Published: April 1, 2026
Distribution: Product was shipped to the following sta…

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FDA Recall United States TerminatedTerminated: May 8, 20262026 recordClass II

American Laboratories, LLC

Product: Pepsin 1:3000 Powder, 50 kg, Item #FTI-G0193-00, American La…
Reason: Potential Salmonella contamination.
Published: April 1, 2026
Distribution: 11 direct wholesale accounts located in…

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FDA Recall United States TerminatedTerminated: May 8, 20262026 recordClass II

American Laboratories, LLC

Product: Pepsin 1:10,000 Powder, 10 kg, Item #FTI-G0193-00, American…
Reason: Potential Salmonella contamination.
Published: April 1, 2026
Distribution: 11 direct wholesale accounts located in…

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FDA Recall United States TerminatedTerminated: May 8, 20262026 recordClass II