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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.

37,059
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
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 1,181–1,200 of 22,574 recalls

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 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 Ongoing Historical recordClass I

EGGS UNLIMITED LLC

Product
Big Y Brown Jumbo A 12ct Eggs; UPC: 018894319146 Simple Trut…
Reason
Firm received, repackaged eggs that are potentially contamination with Salmonella.
Published
November 12, 2025
Distribution
Product was distributed to 3 retail cons…

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

Lisdexamfetamine Dimesylate Capsules, 30 mg, CII, 100-count bottle, Rx only, Manufactured by: OHM Laboratories, New Brunswick, NJ 08901, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, NDC 57664-048-88.

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason
Failed Dissolution Specifications: An out of specification results observed in dissolution test during analysis at 12-month long term stability station (25¿C, 60%RH) for Lisdexamfetamine dimesylate capsules.
Published
November 5, 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.