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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.

37,339
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,860
Class I recallsReasonable probability of serious health consequences
24,450
Class II recallsTemporary or medically reversible health consequences
2,901
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 2,095 recalls
Newest recallhttps://www.fsis.usda.gov/recalls-alerts/imperio-distribution-llc-recalls-beef-jerky-products-produced-without-benefitPublished October 24, 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 II24,450
Class I9,860
Class III2,901
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,450
Class I9,860
Class III2,901
Not Yet Classified2

Showing 1,381–1,400 of 25,393 recalls

FDA Recall United States TerminatedTerminated: February 25, 2026Historical recordClass II

HANA GROUP

Product
Mai California Roll WR - UPC 840031402639 5.9 oz (167g) Pla…
Reason
Wheat and Soy missing allergens from the product Contains Statement.
Published
November 19, 2025
Distribution
(FL, VA, IL, NE, MN, IN, LA, OK) - retai…

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FDA Recall United States TerminatedTerminated: February 6, 2026Historical recordClass I

JFE FRANCHISING INC

Product
Peach Salsa - $5.99-16 oz 639123940636 packaged in clear pla…
Reason
Peaches provided by Moonlight Peaches potentially contaminated with Listeria.
Published
November 19, 2025
Distribution
Multiple states

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FDA Recall United States TerminatedTerminated: February 3, 2026Historical recordClass I

GBC Food Services, LLC

Product
Peach Salsa; UPC 85006540364 14oz (397g); Use by 10/12/2025…
Reason
Peaches provided by Moonlight Peaches potentially contaminated with Listeria.
Published
November 19, 2025
Distribution
IL, CO, GA, WA, IN, MS, TN, AR, OR, MI.

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FDA Recall United States TerminatedTerminated: November 25, 2025Historical recordClass I

Seoul Trading, Inc.

Product
Item IL1014A, PIGGY Lotte Crispy Crunch Ice Cream Cone, Stra…
Reason
Undeclared peanut.
Published
November 19, 2025
Distribution
Distributed in OR and WA

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FDA Recall United States TerminatedTerminated: March 26, 2026Historical recordClass I

Lotus Vaping Technologies, LLC

Product
Monarch Premium Kratom White Elephant powder is packaged in…
Reason
Product has the potential to be contaminated with Salmonella
Published
November 19, 2025
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: March 26, 2026Historical recordClass I

Lotus Vaping Technologies, LLC

Product
Monarch Premium Kratom Red Bali powder is packaged in seal m…
Reason
Product has the potential to be contaminated with Salmonella
Published
November 19, 2025
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: March 26, 2026Historical recordClass I

Lotus Vaping Technologies, LLC

Product
Monarch Premium Kratom Green Maeng Da powder is packaged in…
Reason
Product has the potential to be contaminated with Salmonella
Published
November 19, 2025
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: March 26, 2026Historical recordClass I

Lotus Vaping Technologies, LLC

Product
Monarch Premium Kratom Bali Gold powder is packaged in seal…
Reason
Product has the potential to be contaminated with Salmonella
Published
November 19, 2025
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: December 31, 2025Historical recordClass II

Professional Botanicals, Inc.

Product
Product Name: Tense-X. Package: 175cc HDPE Bottle. Type: Veg…
Reason
Products contains Magnesium Salicylate.
Published
November 19, 2025
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: December 31, 2025Historical recordClass II

Professional Botanicals, Inc.

Product
Product Name: Total Comfort. Package: 175cc HDPE Bottle. Typ…
Reason
Products contains Magnesium Salicylate.
Published
November 19, 2025
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: December 31, 2025Historical recordClass II

Professional Botanicals, Inc.

Product
Product Name: Nutra Calm Package: 175cc HDPE Bottle. Type: V…
Reason
Products contains Magnesium Salicylate.
Published
November 19, 2025
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: April 20, 2026Historical recordClass II

FreshRealm

Product
Loaded Veggie Grain Bowl; Net Wt. 10.90 Oz (309g) GTIN code:…
Reason
Potential contamination with Listeria monocytogenes
Published
November 19, 2025
Distribution
Product was manufactured and shipped dir…

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FDA Recall United States TerminatedTerminated: January 16, 2026Historical recordClass I

Zingerman's Coffee Company

Product
Zingerman's Ca$hew Cow Candy Bar net wt 2oz UPC 844397000157
Reason
Undeclared peanut
Published
November 19, 2025
Distribution
This product was distributed to retailer…

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FDA Recall United States TerminatedTerminated: January 16, 2026Historical recordClass I

Zingerman's Coffee Company

Product
Zingerman's Peanut Butter Crush Candy Bar net wt 2oz UPC 844…
Reason
Undeclared cashew
Published
November 19, 2025
Distribution
This product was distributed to retailer…

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FDA Recall United States TerminatedTerminated: March 19, 2026Historical recordClass II

Blue Oven Bakery, Inc.

Product
Blue Oven Artisan Bakery English Muffins, Net Wt. 13.4 oz (3…
Reason
Undeclared allergen - milk
Published
November 19, 2025
Distribution
Product distributed to 5 retailers in IN…

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FDA Recall OngoingHistorical recordClass II

Acetaminophen 500mg Caffeine 65mg caplets, packaged as 2 caplets per packet further packaged in a 50-count box, AERO TAB, Manufactured for AERO HEALTHCARE US, Valley-Cottage, NY, 10989, NDC 55305-135-01

by Aero Healthcare

Reason
Labeling: Label Mix-up. This issue affects the outer box labeling only. The box incorrectly states the ingredients Acetaminophen 500mg and Caffeine 65mg. The inner pouch correctly states the ingredients are Aspirin (NSAID)*500mg and Caffeine 32.5mg.
Published
November 12, 2025
Distribution
Nationwide

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FDA Recall OngoingHistorical recordClass II

clomiPRAMINE Hydrochloride, Capsules, USP, 75 mg, packaged in a) 30-count bottles (NDC 16714-851-01), b) 90-count bottles (NDC 16714-851-02), c) 100 capsules, NDC 16714-851-03 Rx only, Manufactured for: Northstar Rx LLC, Memphis, TN 38141, Manufactured by: Zydus Lifesciences Ltd., Ahmedabad, India.

by Zydus Pharmaceuticals (USA) Inc

Reason
cGMP deviations: an observed Out of Specification of Nitrosamine Drug Substance-Related Impurities (NDSRIs), N-Nitroso Desmethyl-Clomipramine, above the FDA acceptable intake limit.
Published
November 12, 2025
Distribution
Nationwide

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FDA Recall OngoingHistorical recordClass II

clomiPRAMINE Hydrochloride, Capsules, USP, 50 mg, packaged in a) 30-count bottles (NDC 16714-850-01), b) 90-count bottles (NDC 16714-850-02), c) 100-count bottles (NDC 16714-850-03), Rx only, Manufactured for: Northstar Rx LLC, Memphis, TN 38141, Manufactured by: Zydus Lifesciences Ltd., Ahmedabad, India

by Zydus Pharmaceuticals (USA) Inc

Reason
cGMP deviations: an observed Out of Specification of Nitrosamine Drug Substance-Related Impurities (NDSRIs), N-Nitroso Desmethyl-Clomipramine, above the FDA acceptable intake limit.
Published
November 12, 2025
Distribution
Nationwide

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FDA Recall OngoingHistorical recordClass II

clomiPRAMINE Hydrochloride, Capsules, USP, 25 mg, packaged in a) 30-count bottles (NDC 16714-849-01), b) 90-count bottles (NDC 16714-849-02), c) 100-count bottles (NDC 16714-849-03), Rx only, Manufactured for: Northstar Rx LLC, Memphis, TN 38141, Manufactured by: Zydus Lifesciences Ltd., Ahmedabad, India

by Zydus Pharmaceuticals (USA) Inc

Reason
cGMP deviations: an observed Out of Specification of Nitrosamine Drug Substance-Related Impurities (NDSRIs), N-Nitroso Desmethyl-Clomipramine, above the FDA acceptable intake limit.
Published
November 12, 2025
Distribution
Nationwide

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FDA Recall OngoingHistorical recordClass II

Amoxicillin and Clavulanate Potassium for Oral Suspension USP, 200 mg/28.5 mg per 5mL, 100 mL (when reconstituted), Rx only, manufactured in Canada by: Teva Canada Limited, Toronto, Canada M1B 2K9; Manufactured For: Teva Pharmaceuticals USA, Inc., Parsippany, NJ 07054 NDC 0093-2277-7.

by Teva Pharmaceuticals USA, Inc

Reason
Subpotent drug; Clavulanate Potassium component
Published
November 12, 2025
Distribution
Distributed in three (3) States: MS, OH,…

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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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