Data Explorer

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Recall totals

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

37,449

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,872

Class I recallsReasonable probability of serious health consequences

24,509

Class II recallsTemporary or medically reversible health consequences

2,932

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 2,096 recalls

Newest recallhttps://www.fsis.usda.gov/recalls-alerts/fsis-issues-public-health-alert-meat-and-poultry-products-due-misbranding-andPublished November 6, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated November 9, 2026 ET

Summary (Year to date)

1,956 recalls have been announced year to date.
Oct 2026 was 4% higher than the previous complete period (Sep 2026: 209).
The highest complete period was Jun 2026 (300).
Nov 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,509
Class I	9,872
Class III	2,932
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,509
Class I	9,872
Class III	2,932
Not Yet Classified	2

FDA Recall TerminatedTerminated: April 23, 2018Historical recordClass III

Carbamazepine Oral Suspension USP, 100 mg/5 mL, 5 mL Unit Dose Cups (NDC 68094-301-59), packaged in 10-count cups per tray, 3 trays per case containing a total of 5 mL x 30 Unit Dose Cups per case (NDC 68094-301-62), Rx only, Pkg: Precision Dose, Inc., S. Beloit, IL 61080.

by Precision Dose Inc.

Reason: Subpotent Drug: low out of specification results.
Published: November 8, 2017
Distribution: Nationwide

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FDA Recall TerminatedTerminated: May 13, 2020Historical recordClass III

Clofarabine injection, 20 mg/20 mL, 20 mL Single-Use Vial, Rx only, Mfd by: Teva Pharmachemle, Swensweg 5, Haarlem, The Netherlands; Mfd for: Winthrop U.S., a business of sanofi-aventis U.S. LLC, Bridgewater, NJ 08807; NDC 0955-1746-01.

by Sanofi-Aventis U.S. LLC

Reason: Labeling: Incorrect or Missing Package Insert: authorized generic product was packaged with the incorrect insert for the brand name product Clolar (clofarabine) injection.
Published: November 8, 2017
Distribution: Nationwide

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FDA Recall TerminatedTerminated: March 11, 2019Historical recordClass II

Duloxetine Delayed-release Capsules USP, 20 mg, 50 Capsules (5 x 10) Unit Dose per carton, unit dose blister UPC 5026828311), Rx only, Manufactured for: AvKARE, Inc., Pulaski, TN 38478, NDC 50268-283-15.

by AVKARE Inc.

Reason: Failed Impurities/Degradation Specifications: slightly elevated levels of phthalic acid.
Published: November 8, 2017
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: November 21, 2017Historical recordClass I

Earthbound Farm, LLC

Product: Earthbound Farm¿ Organic Chopped Asian Style Salad Kit; 11 o…
Reason: Recall of Asian Style Chopped Salad Kit because in some instances the dressing and toppings packets inside the bag are not those foe the salad. Some of the Asian Style Salad Kits could have the dressing packet for the Southwest Chopped Salad Kit which contains egg and milk that are not declared as ingredients on the bag of the Asian Style Salad Kit.
Published: November 8, 2017
Distribution: Alaska, Arizona, California, Colorado, F…

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FDA Recall United States TerminatedTerminated: January 8, 2018Historical recordClass I

Organic Spices, Inc

Product: Spicely Organics Organic Tarragon 0.4oz. (11g) UPC codes:…
Reason: Potential Salmonella contamination.
Published: November 8, 2017
Distribution: U.S. distribution to the following: Alas…

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FDA Recall United States TerminatedTerminated: December 28, 2017Historical recordClass I

Tres Latin Foods

Product: Tres Latin Foods Pupusas, Stuffed Corn Tortillas with Black…
Reason: Tres Latin Foods is recalling specific code dates of Kale & Pinto Bean 10 oz. Pupusas and Black Bean and Sweet Corn 10 oz. Pupusas due to undeclared milk allergen.
Published: November 8, 2017
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: December 28, 2017Historical recordClass I