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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.

37,063
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/evergreen-fresh-sprouts-llc-recalls-broccoli-sprouts-because-possible-health-riskPublished September 10, 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 2,641–2,660 of 18,528 recalls

FDA Recall Ongoing Historical recordClass II

KinderMed KIDS' PAIN & FEVER Acetaminophen, 160 mg per 5 mL bottles, Oral Suspension, Organic Cherry Flavor, 4 FL OZ (118 mL), Distributed By: KinderFarms, Redondo Beach, CA 90277, NDC 82673-097-04, UPC 850001805728.

by KINDER FARMS LLC

Reason
Failed Impurities/Degradation Specifications
Published
December 13, 2023
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

LET Gel (Lidocaine HCL/Epinephrine Bitartrate/Tetracaine HCL 4%/0.18%/0.5% Topical Gel), Single-use Topical Syringe, 3mL syringe, 10/pack, Rx only, Carie Boyd Pharmaceuticals, 8400 Esters Blvd, Ste# 190, Irving, TX 75063, NDC73271-1003-1

by Right Value Drug Stores, LLC dba Carie Boyd's Prescription Shop

Reason
Product Mix-up: Incorrect Product Formulation
Published
December 13, 2023
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Trospium Chloride Extended-Release Capsules, 60 mg, 30 Capsules per bottle, Rx Only, Manufactured By: Sidmak Laboratories (India) Pvt. Ltd. Plot No. 20, Pharmacity, Selaqui Industrial Area, Dehradun-248 197 Uttarakhand, India Distributed By: Padagis, Allegan, MI 49010. NDC: 0574-0118-30

by Padagis US LLC

Reason
Failed Tablets/Capsules specifications; missing/broken/extra tablets within the capsules
Published
December 13, 2023
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass I

Dr. Ergin's SugarMD, ADVANCED GLUCOSE SUPPORT Capsules, Dietary Supplement, helps support healthy glucose levels a) 60 count (UPC 1 95893 92767 8), b) 120 count (UPC 1 95893 54697 8), c) 180 count (UPC 1 95893 99957 6) bottles, Manufactured for SUGARMDS LLC, Port St. Lucie, FL 34952.

by SUGARMDS LLC

Reason
MARKETED WITHOUT AN APPROVED NDA/ANDA: Product found to be tainted with metformin and glyburide
Published
December 13, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

buPROPion Hydrochloride Extended-Release Tablets, USP (SR) 200 mg, 60 Tablets bottle, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, Manufactured by: Sun Pharmaceutical Industries Limited, Halol-Baroda Highway, Halol-389 350, Gujarat, India NDC 47335-738-86

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason
Failed Dissolution Specifications
Published
December 13, 2023
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

FreshPoint Bix Produce Company, LLC

Product
Bix Produce Item # 12217 Fruit, Chk Cant/Pine 1/2" w/Grp, 5…
Reason
Potential Salmonella contamination.
Published
December 13, 2023
Distribution
Multiple states

View recall →

FDA Recall United States Terminated Historical 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

View recall →

FDA Recall United States Terminated Historical 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

View recall →

FDA Recall United States Terminated Historical 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

View recall →

FDA Recall United States Terminated Historical 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

View recall →

FDA Recall United States Terminated Historical 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

View recall →

FDA Recall United States Terminated Historical 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

View recall →

FDA Recall United States Terminated Historical 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

View recall →

FDA Recall United States Terminated Historical 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…

View recall →

FDA Recall United States Terminated Historical 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…

View recall →

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

View recall →

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

View recall →

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

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.