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Recall totals

All FDA and USDA recalls in Public Health Trace, June 2012 to October 2026.

37,269

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

State: MN ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated October 17, 2026 ET

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

Recalls by class
Class	Recalls
Class II	24,397
Class I	9,852
Class III	2,897
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,397
Class I	9,852
Class III	2,897
Not Yet Classified	2

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: March 20, 2026Historical 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 TerminatedTerminated: March 20, 2026Historical 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 TerminatedTerminated: March 20, 2026Historical 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 TerminatedTerminated: March 20, 2026Historical 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 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: August 12, 2026Historical 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 TerminatedTerminated: August 12, 2026Historical recordClass II