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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.

37,268
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 recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/family-farmstead-dairy-announces-recall-raw-mild-cheddar-cheese-due-potential-e-coli-o157h7Published October 15, 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 1,161–1,180 of 21,683 recalls

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 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 United States TerminatedTerminated: April 14, 2026Historical 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 OngoingHistorical 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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FDA Recall United States OngoingHistorical recordClass II

Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

Product
Publix Extra Large Shrimp Easy to Peel Deveined 21/25, net w…
Reason
Shrimp may be contaminated with Cesium-137 (Cs-137).
Published
November 12, 2025
Distribution
Nationwide

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FDA Recall United States OngoingHistorical recordClass II

Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

Product
AquaStar 13/15 Raw Shrimp Easy Peel Deveined, net wt. 2 lbs.…
Reason
Shrimp may be contaminated with Cesium-137 (Cs-137).
Published
November 12, 2025
Distribution
Nationwide

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FDA Recall United States OngoingHistorical recordClass II

Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

Product
AquaStar 16/20 Frozen Raw EZ-Peel White Shrimp, net wt. 5 lb…
Reason
Shrimp may be contaminated with Cesium-137 (Cs-137).
Published
November 12, 2025
Distribution
Nationwide

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FDA Recall United States OngoingHistorical recordClass II

Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

Product
Waterfront Bistro Frozen Raw EZ-Peel White Shrimp 21/25, net…
Reason
Shrimp may be contaminated with Cesium-137 (Cs-137).
Published
November 12, 2025
Distribution
Nationwide

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FDA Recall United States OngoingHistorical recordClass II

Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

Product
Best Yet Frozen Raw EZ-Peel White Shrimp 16/20 (net wt. 1 l…
Reason
Shrimp may be contaminated with Cesium-137 (Cs-137).
Published
November 12, 2025
Distribution
Nationwide

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FDA Recall United States OngoingHistorical recordClass II

Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

Product
AquaStar Raw Peeled Tail-on Shrimp Skewers, net wt. 1.25lbs.…
Reason
Shrimp may be contaminated with Cesium-137 (Cs-137).
Published
November 12, 2025
Distribution
Nationwide

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FDA Recall United States OngoingHistorical recordClass II

Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

Product
Kroger Mercado Cooked Medium Peeled Tail-Off Shrimp, net wt.…
Reason
Shrimp may be contaminated with Cesium-137 (Cs-137).
Published
November 12, 2025
Distribution
Nationwide

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FDA Recall United States OngoingHistorical recordClass II

Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

Product
Kroger Raw Colossal EZ Peel Shrimp, net wt. 2lbs., UPC 20011…
Reason
Shrimp may be contaminated with Cesium-137 (Cs-137).
Published
November 12, 2025
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: April 30, 2026Historical recordClass II

Eagle Spice and Extract Co., Inc.

Product
Eagle Spice Ground Ginger 16 oz.
Reason
Contains elevated levels of lead (Pb)
Published
November 12, 2025
Distribution
Multiple states

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.