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Recall totals

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

37,266

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/pan-pepin-inc-emite-alerta-por-alergenos-en-el-producto-parabien-al-grano-debido-la-presencia-dePublished October 13, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated October 15, 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 Ongoing2026 recordClass II

Duloxetine DR Capsules, 30 mg, 30 count bottles, Rx, Relabeled by: Enovachem Pharmaceuticals, Torrance, CA 90501, NDC 76420-634-30, Marketed by: Ajanta Pharma USA Inc.

by Asclemed USA Inc.

Reason: CGMP Deviations; presence of Nitrosamine Drug Substance Related Impurity (NDSRI), N-nitroso-duloxetine, above the FDA acceptable intake limit.
Published: June 10, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

Lidocaine HCl Injection USP, 25x5 mL, Single-Dose Ampules, Rx Only, Distributed by: Spectra Medical Devices, LLC, Wilmington, Made in S. Korea, NDC 65282-1605-1.

by Spectra Medical Devices, Llc

Reason: Lack of Assurance of Sterility
Published: June 10, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass III

Lidocaine HCl Injection, USP 2%, 40 mg/2 mL (20 mg/mL), 2 mL per Single-Dose Vial, Rx Only, Mfd. in India for: Eugia US LLC, E. Windsor, NJ 08520. NDC: 55150-164-02

by Eugia US LLC

Reason: Labeling: Not Elsewhere Classified: The label wrap covers the barcode, making it hard to scan
Published: June 10, 2026
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: July 2, 20262026 recordClass II

Albertsons Companies LLC

Product: UPC 22019700000 PAVILIONS CHOCOLATE COVERED STRAWBERRY 1 CT…
Reason: Contains statement does not declare Hazelnut
Published: June 10, 2026
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: July 2, 20262026 recordClass II

Albertsons Companies LLC

Product: UPC 21477700000 Ready Meals SALAD FRESH BERRY & SALMON SS CO…
Reason: Contains statement does not declare Salmon and Walnut
Published: June 10, 2026
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: July 2, 20262026 recordClass II