Data Explorer

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Recall totals

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

37,341

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,860

Class I recallsReasonable probability of serious health consequences

24,450

Class II recallsTemporary or medically reversible health consequences

2,901

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 2,095 recalls

Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/haifa-smoked-fish-recalls-cold-smoked-sprats-due-potential-health-riskPublished October 27, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated October 28, 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	24,450
Class I	9,860
Class III	2,901
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,450
Class I	9,860
Class III	2,901
Not Yet Classified	2

FDA Recall OngoingHistorical recordClass II

CVS Health Concealing Acne Treatment Cream, CVS, 10% benzoyl peroxide, 1 oz (28 g), Distributed by: CVS Pharmacy, Inc

by Fruit Of The Earth, Inc.

Reason: Chemical contamination: presence of benzene
Published: March 26, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Walgreens Maximum Strength Tinted Acne Treatment Cream 10% Benzoyl Peroxide/Acne Medication, 0.65 oz (18.4g) tube in a carton; Distributed by: Walgreen CO., 200 Wilmot Rd., Deerfield, IL 60015

by Fruit Of The Earth, Inc.

Reason: Chemical contamination: presence of benzene
Published: March 26, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Ciprofloxacin Ophthalmic Solution USP, 0.3% as base, package in 5 mL bottles, Rx Only, Distributed by: Leading Pharma LLC, Fairfield, NJ. Manufactured by: FDC Limited, Maharashtra, India, NDC 69315-308-05

by FDC Limited

Reason: Defective container: Unable to get the solution out of the bottle as the spike of the cap was lodged in the nozzle of the product bottle
Published: March 26, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass I

Vitality, Fast Acting Male Enhancement Product, Dietary Supplement, a) One Capsule per Packet, b) 6 capsules per bottle, Xtreme Potency.

by One Source Nutrition, Inc,

Reason: Marketed without an approved NDA/ANDA: Product found to be tainted with undeclared sildenafil and tadalafil.
Published: March 26, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Prasugrel Tablets, USP, 5 mg, 30-count bottle, Rx only, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 U.S.A., NDC 0378-5185-93

by MYLAN PHARMACEUTICALS INC

Reason: Failed Dissolution Specifications - low dissolution results
Published: March 26, 2025
Distribution: Nationwide

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FDA Recall CompletedHistorical recordClass II

Cinacalcet Hydrochloride Tablets 60 mg, 30-count bottle, Rx only, Distr. by: Slate Run Pharma., LLC, Columbus, Ohio 43215, Mfg. by: Piramal Pharma Limited, Madhya Pradesh, India, NDC 70436-008-04

by Slate Run Pharmaceuticals

Reason: CGMP deviations: The presence of nitrosamine impurity above the acceptable daily intake limits.
Published: March 26, 2025
Distribution: Nationwide

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FDA Recall CompletedHistorical recordClass II

Cinacalcet Hydrochloride Tablets 30 mg, 30-count bottle, Rx only, Distr. by: Slate Run Pharma., LLC, Columbus, Ohio 43215, Mfg. by: Piramal Pharma Limited, Madhya Pradesh, India, NDC 70436-007-04

by Slate Run Pharmaceuticals

Reason: CGMP deviations: The presence of nitrosamine impurity above the acceptable daily intake limits.
Published: March 26, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II