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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 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

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)

  • 1,739 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

A bar chart of the total number of recalls in this dataset by recall class.

Recalls by class
ClassRecalls
Class II24,397
Class I9,852
Class III2,897
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,397
Class I9,852
Class III2,897
Not Yet Classified2

Showing 2,261–2,280 of 20,472 recalls

FDA Recall TerminatedTerminated: August 15, 2025Historical recordClass II

Phenylephrine HCl 0.9% Sodium Chloride Injection USP, 10 mg per 250 mL, Single Dose Bag, Rx only, Fagron Sterile Services, Canton, MA NDC 71506-029-58

by Fresenius Kabi Compounding, LLC

Reason
cGMP violations
Published
October 30, 2024
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: August 15, 2025Historical recordClass II

Phenylephrine HCl 0.9% Sodium Chloride Injection USP, 10 mg per 250 mL, Single Dose Bag, Rx only, Fagron Sterile Services, Canton, MA NDC 71506-010-58

by Fresenius Kabi Compounding, LLC

Reason
cGMP violations
Published
October 30, 2024
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: August 15, 2025Historical recordClass II

Phenylephrine HCl 0.9% Sodium Chloride Injection USP, 20 mg per 250 mL, Single Dose Bag, Rx only, Fagron Sterile Services, Canton, MA NDC 71506-024-58

by Fresenius Kabi Compounding, LLC

Reason
cGMP violations
Published
October 30, 2024
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: August 15, 2025Historical recordClass II

Phenylephrine HCl 0.9% Sodium Chloride Injection USP, 20 mg per 250 mL, Single Dose Bag, Rx only, Fagron Sterile Services, Canton, MA NDC 71506-002-58

by Fresenius Kabi Compounding, LLC

Reason
CGMP violations
Published
October 30, 2024
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: April 14, 2025Historical recordClass II

Youngstown Grape Distributors, Inc.

Product
Farmers Juice Watermelon Hydration packaged in a 12 fl. oz.…
Reason
Incomplete pasteurization
Published
October 30, 2024
Distribution
CA, TX, WA, KY, NC, NY, IL, VA, AL, GA,…

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FDA Recall United States TerminatedTerminated: April 14, 2025Historical recordClass II

Youngstown Grape Distributors, Inc.

Product
Farmers Juice Carrot Digest packaged in a 12 fl. oz. bottle;…
Reason
Incomplete pasteurization
Published
October 30, 2024
Distribution
CA, TX, WA, KY, NC, NY, IL, VA, AL, GA,…

View recall →

FDA Recall United States TerminatedTerminated: April 14, 2025Historical recordClass II

Youngstown Grape Distributors, Inc.

Product
Farmers Juice Focus Greens packaged in a 12 fl. oz. bottle;…
Reason
Incomplete pasteurization
Published
October 30, 2024
Distribution
CA, TX, WA, KY, NC, NY, IL, VA, AL, GA,…

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FDA Recall United States TerminatedTerminated: April 14, 2025Historical recordClass II

Youngstown Grape Distributors, Inc.

Product
Happy Moose Juice Strawberry Field packaged in a plastic 12…
Reason
Incomplete pasteurization
Published
October 30, 2024
Distribution
CA, TX, WA, KY, NC, NY, IL, VA, AL, GA,…

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FDA Recall United States TerminatedTerminated: April 14, 2025Historical recordClass II

Youngstown Grape Distributors, Inc.

Product
Happy Moose Juice Tropical Roots packaged in a plastic 12 fl…
Reason
Incomplete pasteurization
Published
October 30, 2024
Distribution
CA, TX, WA, KY, NC, NY, IL, VA, AL, GA,…

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FDA Recall United States TerminatedTerminated: April 11, 2025Historical recordClass I

HP Hood LLC

Product
Lactaid Lactose Reduced milk 1. 96 oz Lactaid Whole Milk 2.…
Reason
Milk may contain undeclared almond from almond milk
Published
October 30, 2024
Distribution
AL, CO, CT, FL, GA, IA, IL, IN, KS, KY,…

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FDA Recall OngoingHistorical recordClass II

First Aid Antiseptic Ointment, Povidone Iodine USP 10%, Inactive Ingredients: mineral oil, petrolatum. NET Wt. 1 OZ (28.4 g) per tube, Distributed by: Rugby Laboratories, Indianapolis, IN 46268. Made in China. NDC: 0536-1271-80

by Zhejiang Jingwei Pharmaceutical Co., Ltd.

Reason
Incorrect/Undeclared Excipients: The inactive ingredients labeled on the product boxes and tubes are listed as "mineral oil , petrolatum ". The inactive ingredients in the actual product are polyethylene glycol 400 , polyethylene glycol 4000.
Published
October 23, 2024
Distribution
Nationwide

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FDA Recall TerminatedTerminated: September 16, 2025Historical recordClass I

Atovaquone Oral Suspension, USP 750 mg/5 mL, 210 mL bottle, Rx only, Distributed by: Bionpharma Inc., Princeton, NJ 08540, NDC # 69452-252-87.

by Bionpharma Inc.

Reason
Microbial Contamination of a Non-sterile Product: The product was found to be contaminated with Cohnella bacteria.
Published
October 23, 2024
Distribution
Nationwide

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FDA Recall TerminatedTerminated: February 23, 2026Historical recordClass II

Cisplatin Injection, 100mg/100mL (1mg/mL), For Intravenous Use, 100 mL Multiple Dose Vial, Rx Only, Manufactured for: Accord Healthcare Inc., Durham, NC 27703. Manufactured by: Intas Pharmaceuticals Limited, Pharmez, Ahmedabad 382 213, India. Mfg. Lic. No.: G/28/1336, NDC 16729-288-38

by ACCORD HEALTHCARE, INC.

Reason
Failed Impurities/Degradation Specifications.
Published
October 23, 2024
Distribution
Nationwide

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FDA Recall CompletedHistorical recordClass II

Duloxetine Delayed-Release Capsules, USP, 20mg, Rx Only, 500-count bottles, Mfr. by: Towa Pharmaceutical Europe, S.L. Distributed by: BPI, NDC 51991-746-05.

by Breckenridge Pharmaceutical, Inc

Reason
CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit
Published
October 23, 2024
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: February 10, 2025Historical recordClass II

Tropical Nut & Fruit Company

Product
Grabeez The Big Cheese SNACK MIX Net Wt. 3.25 oz (92g) Ingre…
Reason
Undeclared Almonds & Cashews. The firm was notified by their customers that the product contains a trail mix instead of the cheese mix. The trail mix contains almonds and cashews that are not listed in the ingredient statement.
Published
October 23, 2024
Distribution
Products distributed to warehouses, reta…

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

Gorilla Mind LLC

Product
Gorilla Mind Rauwolscine Dietary Supplement, Suppress Appeti…
Reason
Product was recalled due to the potential for contamination with Salmonella
Published
October 23, 2024
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: October 29, 2024Historical recordClass II

Lund Food Holdings Inc

Product
Lunds & Byerlys lone star dip. Net Wt 12 oz. (340.5g) UPC…
Reason
Potential mold contamination.
Published
October 23, 2024
Distribution
MN

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FDA Recall United States TerminatedTerminated: June 23, 2025Historical recordClass II

Hydration Labs Inc. dba Bevi

Product
Flavor#115 Electrolytes, Net Contents 3.78L, #740-0115, GTIN…
Reason
Product is labeled as electrolytes but is actually caffeine
Published
October 23, 2024
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: January 29, 2025Historical recordClass III

Walmart Inc

Product
Great Value Cherry Mixed Fruit, 4 oz, 4 Count and 12 count p…
Reason
FD&C Red No 3 was not declared as an ingredient.
Published
October 23, 2024
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: January 29, 2025Historical recordClass III

Walmart Inc

Product
Great Value Diced Peaches, Mandarin Segments, & Cherry Mixed…
Reason
FD&C Red No 3 was not declared as an ingredient.
Published
October 23, 2024
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.

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