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Recall totals

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

37,271

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,852

Class I recallsReasonable probability of serious health consequences

24,397

Class II recallsTemporary or medically reversible health consequences

2,897

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 2,085 recalls

Newest recallhttps://www.fsis.usda.gov/recalls-alerts/kayem-foods-inc--recalls-meat-and-poultry-products-due-possible-temperature-abusePublished October 17, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated October 19, 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	24,397
Class I	9,852
Class III	2,897
Not Yet Classified	2

Recalls by class
Class	Recalls
Class II	24,397
Class I	9,852
Class III	2,897
Not Yet Classified	2

FDA Recall United States TerminatedTerminated: January 15, 2025Historical recordClass I

FreshPoint Bix Produce Company, LLC

Product: Bix Produce Item # 12170 Fruit, Chunk Melon w/Grape 5 lb. co…
Reason: Potential Salmonella contamination.
Published: December 13, 2023
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: January 15, 2025Historical recordClass I

FreshPoint Bix Produce Company, LLC

Product: Bix Produce Mixed Fruit products containing Cantaloupe, Hone…
Reason: Potential Salmonella contamination.
Published: December 13, 2023
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: January 15, 2025Historical recordClass I

FreshPoint Bix Produce Company, LLC

Product: Bix Produce Mixed Fruit with Grapes products containing Cant…
Reason: Potential Salmonella contamination.
Published: December 13, 2023
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: January 15, 2025Historical recordClass I

FreshPoint Bix Produce Company, LLC

Product: Bix Produce Cut Cantaloupe. Keep Refrigerated. Manufactur…
Reason: Potential Salmonella contamination.
Published: December 13, 2023
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: January 15, 2025Historical recordClass I

FreshPoint Bix Produce Company, LLC

Product: Mixed Fruit Cup, clam-shell container. Net Wt 5.75 oz (16…
Reason: Potential Salmonella contamination.
Published: December 13, 2023
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: January 15, 2025Historical recordClass I

FreshPoint Bix Produce Company, LLC

Product: Cantaloupe Fruit Cup, Item 19703. clam-shell container. Ne…
Reason: Potential Salmonella contamination.
Published: December 13, 2023
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: January 15, 2025Historical recordClass I

FreshPoint Bix Produce Company, LLC

Product: FreshPoint Bix Produce Company, Whole Cantaloupe, Item 03143…
Reason: Potential Salmonella contamination.
Published: December 13, 2023
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: September 17, 2024Historical recordClass I

Sofia Produce, L.L.C.

Product: Whole cantaloupe, Brand name Rudy 11 count carton, 8 count c…
Reason: The affected product is being recalled from the marketplace due to possible Salmonella contamination.
Published: December 13, 2023
Distribution: Customers are located in the United Stat…

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FDA Recall United States TerminatedTerminated: September 17, 2024Historical recordClass I

Sofia Produce, L.L.C.

Product: Whole cantaloupe, Brand name Malichita 11 count carton, 8 co…
Reason: The affected product is being recalled from the marketplace due to possible Salmonella contamination.
Published: December 13, 2023
Distribution: Customers are located in the United Stat…

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FDA Recall United States TerminatedTerminated: June 26, 2024Historical recordClass II

Stonewall Kitchen, LLC

Product: Vermont Village Organic Unsweetened Apple Sauce (24oz); UPC…
Reason: Product contains elevated levels of patulin
Published: December 13, 2023
Distribution: Multiple states

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FDA Recall OngoingHistorical 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 OngoingHistorical 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 OngoingHistorical 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 TerminatedTerminated: May 29, 2024Historical 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 TerminatedTerminated: March 21, 2025Historical 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 TerminatedTerminated: March 21, 2025Historical 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

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FDA Recall TerminatedTerminated: March 21, 2025Historical 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

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FDA Recall TerminatedTerminated: June 3, 2024Historical 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

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FDA Recall TerminatedTerminated: July 26, 2024Historical recordClass III

Aminocaproic Acid Oral Solution, 0.25 grams/mL, Rx only, packaged in 8 Fl. Oz. (236.5 mL) HDPE bottles, Manufactured for: VistaPharm, Inc., Largo, FL 33771, UAS, NDC 66689-330-08

by VistaPharm LLC

Reason: Failed Excipient Specifications: high content of ethylene glycol (EG)
Published: December 6, 2023
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass III

Tropicamide 1% (10mg/mL), Cyclopentolate 1% (10mg/mL), Phenylephrine 2.5% (25mg/mL), Ketorolac 0.5% (5mg/mL), 5 mL bottles, For Topical Ophthalmic Use Only, Not for IV Use, This is a Compounded Drug, Hospital & Office Use Only, Fagron Sterile Services, 8710 E 34th St N Wichita, KS 67226. NDC 71266-8240-01

by Fagron Compounding Services

Reason: Labeling: Label Mix-Up: The label of a dropper bottle mistakenly states the container is a 0.5mL single-use syringe instead of a 5 mL dropper
Published: December 6, 2023
Distribution: Nationwide

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Data last updated: October 19, 2026 ET

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.