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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.

37,066
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,786
Class I recallsReasonable probability of serious health consequences
24,313
Class II recallsTemporary or medically reversible health consequences
2,876
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
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/whole-foods-market-issues-allergy-alert-undeclared-egg-cabricharme-cheesePublished September 11, 2026
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 II24,313
Class I9,786
Class III2,876
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,313
Class I9,786
Class III2,876
Not Yet Classified2

Showing 3,021–3,040 of 20,481 recalls

FDA Recall United States Ongoing Historical recordClass II

BAPS Shayona

Product
BAPS SHAYONA Burfi Sweetened ricotta fudge Net Wt: 12 Oz 460…
Reason
During an FDA inspection the firm was notified that some of their products contains undeclared soy.
Published
December 13, 2023
Distribution
Product was shipped to the following sta…

View recall →

FDA Recall United States Ongoing Historical recordClass II

BAPS Shayona

Product
BAPS SHAYONA Surti Ghari Sweet dumplings stuffed with minced…
Reason
During an FDA inspection the firm was notified that some of their products contains undeclared soy and Yellow #6.
Published
December 13, 2023
Distribution
Product was shipped to the following sta…

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FDA Recall United States Ongoing Historical recordClass II

BAPS Shayona

Product
BAPS SHAYONA Motichur Ladoo Sweet chickpea flour mini-pearls…
Reason
During an FDA inspection the firm was notified that some of their products contains undeclared Yellow #5 & #6.
Published
December 13, 2023
Distribution
Product was shipped to the following sta…

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FDA Recall United States Ongoing Historical recordClass II

BAPS Shayona

Product
BAPS SHAYONA Mohanthal Fudge-like sweet made with chickpea f…
Reason
During an FDA inspection the firm was notified that some of their products contains undeclared soy, Yellow #5 & #6.
Published
December 13, 2023
Distribution
Product was shipped to the following sta…

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FDA Recall United States Ongoing Historical recordClass II

BAPS Shayona

Product
BAPS SHAYONA Kopra Paak Coconut fudge Net Wt: 12 Oz 460 Rock…
Reason
During an FDA inspection the firm was notified that some of their products contains undeclared soy.
Published
December 13, 2023
Distribution
Product was shipped to the following sta…

View recall →

FDA Recall United States Ongoing Historical recordClass II

BAPS Shayona

Product
BAPS SHAYONA Kesar Penda Ricotta fudge discs flavored with s…
Reason
During an FDA inspection the firm was notified that some of their products contains undeclared soy and Yellow #5 & #6.
Published
December 13, 2023
Distribution
Product was shipped to the following sta…

View recall →

FDA Recall United States Ongoing Historical recordClass II

BAPS Shayona

Product
BAPS SHAYONA Kaju Pista Roll Sweet rolls made from cashew an…
Reason
During an FDA inspection the firm was notified that some of their products contains undeclared Yellow #5 & #6 and Blue 1.
Published
December 13, 2023
Distribution
Product was shipped to the following sta…

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FDA Recall United States Ongoing Historical recordClass II

BAPS Shayona

Product
BAPS SHAYONA Kaju Katri Kesar Cashew fudge flavored with saf…
Reason
During an FDA inspection the firm was notified that some of their products contains undeclared Yellow #5.
Published
December 13, 2023
Distribution
Product was shipped to the following sta…

View recall →

FDA Recall United States Ongoing Historical recordClass II

BAPS Shayona

Product
BAPS SHAYONA Plain Penda Ricotta fudge discs flavored with r…
Reason
During an FDA inspection the firm was notified that some of their products contains undeclared soy.
Published
December 13, 2023
Distribution
Product was shipped to the following sta…

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FDA Recall United States Ongoing Historical recordClass II

BAPS Shayona

Product
BAPS SHAYONA Bundi Ladoo Sweet chickpea flour pearls rolled…
Reason
During an FDA inspection the firm was notified that some of their products contains undeclared Yellow #5, Red 40 & 3 and Green 3.
Published
December 13, 2023
Distribution
Product was shipped to the following sta…

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FDA Recall United States Ongoing Historical recordClass II

BAPS Shayona

Product
BAPS SHAYONA Badam Pista Sandwich Almond and pistachio layer…
Reason
During an FDA inspection the firm was notified that some of their products contains undeclared Yellow #5, Green 3.
Published
December 13, 2023
Distribution
Product was shipped to the following sta…

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FDA Recall United States Ongoing Historical recordClass II

BAPS Shayona

Product
BAPS SHAYONA Anjir Roll Sweet rolls made from fig and nut fi…
Reason
During an FDA inspection the firm was notified that some of their products contains undeclared Yellow #5.
Published
December 13, 2023
Distribution
Product was shipped to the following sta…

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FDA Recall Ongoing Historical recordClass I

Kuka Flex Forte caplets, packaged in 30-count bottles, Manufactured by: Kukamonga, Gonzalez Ortega No 170 Col Centro, 44100 Guadalajara Jal, UPC 0736640810265

by Botanical Be

Reason
Marketed Without an Approved NDA/ANDA: products found to contain undeclared diclofenac.
Published
December 6, 2023
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass I

Reumo Flex caplets, packaged in 30-count boxes, Manufactured by: Grupo Yepenza de Mexico, SA de CV, Comerciantes 5824 Col Arcos de Guadalupe, Zapopan Jal Mexico, UPC 7 502214 014598

by Botanical Be

Reason
Marketed Without an Approved NDA/ANDA: products found to contain undeclared diclofenac.
Published
December 6, 2023
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass I

Artri King Reforzado con Origa y Omega 3 tablets, packaged in 100-count bottles, Manufactured by: Plantas medicinales de Mexico, Melchol Ocampo # 65 Local D, Delegacion Xochimilco CP 16800, Mexico DF, UPC 7 501031 111138

by Botanical Be

Reason
Marketed Without an Approved NDA/ANDA: products found to contain undeclared diclofenac.
Published
December 6, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

VITRAKVI (larotractenib) oral solution, 20mg/mL, 100 mL bottle, Rx only, Manufactured for Bayer HealthCare Pharmaceuticals Inc., Whippany, NJ 07981. NDC 50419-392-01

by Bayer Healthcare Pharmaceuticals Inc.

Reason
Microbial Contamination of Non-Sterile Products: microbial contamination identified as Penicillium brevicompactum observed during routine ongoing stability testing
Published
December 6, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

PAROXETINE tablets, USP, 40 mg, Packaged as a) 30-count bottle, NDC 60429-737-30; b) 90-count bottle NDC 60429-737-90; c)1000-count bottle, NDC 60429-737-10; Rx Only, Manufactured by Apotex, Inc., Toronto, Ontario, Canada, M9L 1T9, Packaged by GSMS, Incorporated, Camarillo, CA 93012.

by Golden State Medical Supply Inc.

Reason
Failed Impurities/Degradation Specifications-Manufacturer Apotex Inc. recalling lots due to Out of specification results for the excipient Amadori Glucose adduct of Paroxetine
Published
December 6, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

PAROXETINE tablets, USP, 20 mg, Packaged as a) 90-count bottle NDC 60429-735-90; b)1000-count bottle, NDC 60429-735-10; Rx Only, Manufactured by Apotex, Inc., Toronto, Ontario, Canada, M9L 1T9, Packaged by GSMS, Incorporated, Camarillo, CA 93012.

by Golden State Medical Supply Inc.

Reason
Failed Impurities/Degradation Specifications-Manufacturer Apotex Inc. recalling lots due to Out of specification results for the excipient Amadori Glucose adduct of Paroxetine
Published
December 6, 2023
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

PAROXETINE tablets, USP, 10 mg, Packaged as a) 30-count bottle, NDC 60429-734-30; b) 90-count bottle NDC 60429-734-90; c)1000-count bottle, NDC 60429-734-10; Rx Only, Manufactured by Apotex, Inc., Toronto, Ontario, Canada, M9L 1T9, Packaged by GSMS, Incorporated, Camarillo, CA 93012.

by Golden State Medical Supply Inc.

Reason
Failed Impurities/Degradation Specifications-Manufacturer Apotex Inc. recalling lots due to Out of specification results for the excipient Amadori Glucose adduct of Paroxetine
Published
December 6, 2023
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Testosterone Gel, 1.62% CIII (Alcohol 80% v/v), packaged in 30 unit-dose packets per carton, Rx only, Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0591-2926-30

by Teva Pharmaceuticals USA, Inc

Reason
OOS for viscosity
Published
December 6, 2023
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.