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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.

37,060
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/freshpoint-issues-recall-due-improperly-declared-allergen-egg-chicken-salad-wedge-sandwichesPublished September 8, 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 1,021–1,040 of 21,559 recalls

FDA Recall United States Terminated Historical 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 Terminated Historical 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

View recall →

FDA Recall United States Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical recordClass I

Pacific International Marketing

Product
Carton Label: PACIFIC STRAIGHT FROM THE FIELDS FRESH HERBS 4…
Reason
Potential contamination with Salmonella.
Published
November 19, 2025
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

Pacific International Marketing

Product
Carton Label: PACIFIC FRESH VEGETABLES PACIFIC INTERNATIONAL…
Reason
Potential contamination with Salmonella.
Published
November 19, 2025
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

Pacific International Marketing

Product
Carton Label: PACIFIC FRESH VEGETABLES PACIFIC INTERNATIONAL…
Reason
Potential contamination with Salmonella.
Published
November 19, 2025
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

Pacific International Marketing

Product
Carton Label: PACIFIC FRESH VEGETABLES PACIFIC INTERNATIONAL…
Reason
Potential contamination with Salmonella.
Published
November 19, 2025
Distribution
Multiple states

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FDA Recall United States Terminated Historical 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 Ongoing Historical 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 Ongoing Historical 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 Ongoing Historical 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 Ongoing Historical 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 Ongoing Historical 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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FDA Recall United States Terminated Historical recordClass II

TBC Distribution Corporate

Product
Lucky Foods Cinnamon Powder; 40g
Reason
Products may contain elevated levels of lead.
Published
November 12, 2025
Distribution
Multiple states

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FDA Recall United States Completed Historical recordClass II

Ice Cream Factory, LLC

Product
Bakery Graham Pieces, 10 LB Label reads in part as "Ice Crea…
Reason
Foreign material fragments consisting of aluminum foil and packaging material were identified in brown sugar ingredient that may have been used in the products
Published
November 12, 2025
Distribution
Consumers, wholesale and retail location…

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FDA Recall United States Completed Historical recordClass II

Ice Cream Factory, LLC

Product
Strawberry Cheesecake Ice Cream with graham crackers swirl,…
Reason
Foreign material fragments consisting of aluminum foil and packaging material were identified in brown sugar ingredient that may have been used in the products
Published
November 12, 2025
Distribution
Consumers, wholesale and retail location…

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FDA Recall United States Ongoing Historical recordClass II

Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

Product
Publix Large Shrimp Peeled & Deveined Tail On 31/40, net wt.…
Reason
Shrimp may be contaminated with Cesium-137 (Cs-137).
Published
November 12, 2025
Distribution
Nationwide

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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.