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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.

37,063
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 2,561–2,580 of 17,805 recalls

FDA Recall Terminated Historical recordClass II

Aripiprazole Tablets, USP, 5 mg, 30 Tablets per bottle, Distributed by: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807. NDC: 65162-897-03

by CARDINAL HEALTHCARE

Reason
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Published
January 3, 2024
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

AMOXICILLIN Tablets, USP, 875MG, 20 Tablets, Rx Only, Manufactured by Sandoz GmbH for Sandoz Inc., Princeton, NJ 08540. NDC: 0781-5060-20

by CARDINAL HEALTHCARE

Reason
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Published
January 3, 2024
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

AMOXICILLIN for Oral Suspension USP, 400MG/5ML, 100ML (when reconstituted), Manufactured In Canada By: TEVA CANA LIMITED, Toronto, Canada M1B 2K9; Manufactured For: TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454. NDC: 0093-4161-73

by CARDINAL HEALTHCARE

Reason
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Published
January 3, 2024
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

ALLOPURINOL Tablets, USP 300 MG 500 count Tablets per bottle, Rx only, Manufactured By: Dr. Reddy's Laboratories LA LLC, Shreveport, LA 71106. NDC: 55111-730-05

by CARDINAL HEALTHCARE

Reason
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Published
January 3, 2024
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

ALBUTEROL SULFATE IN 90MCG per actuation, 200 Metered Inhalations, Rx Only, 8.5 g Net Contents, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, Maryland 21202; Manufactured by: Lupin Limited, Pithampur (M.P.) 454 775, India. NDC: 68180-963-01

by CARDINAL HEALTHCARE

Reason
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Published
January 3, 2024
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

ALBUTEROL SULFATE HFA Inhalation Aerosol, 90MCG per actuation, 200 Metered Inhalations, Net Wt. 18 g, Rx Only, Manufactured for: Prasco Laboratories, Mason, OH 45040 USA. NDC: 66993-019-68

by CARDINAL HEALTHCARE

Reason
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Published
January 3, 2024
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Ipratropium Bromide and Albuterol Sulfate Inhalation Solution (0.5 mg/3 mg per 3 mL), 60 x 3 mL Sterile Unit-Dose Vials (2 pouches of 30 - 3 mL vials each), Manufactured By: The Ritedose Corporation, Columbia, SC 29203; Distributed By: Cipla USA Inc., 10 Independence Boulevard, Suite 300, Warren, NJ 07059. NDC: 69097-840-64

by CARDINAL HEALTHCARE

Reason
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Published
January 3, 2024
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

ANORO ELLIPTA (umeclidinium and vilanterol inhalation powder) 62.5 mcg/25mcg. 1 inhaler contains 30 doses (60 blisters total), Rx Only, Manufactured by GlaxoSmithKline Durham, NC 27701. NDC 0173-0869-10

by GlaxoSmithKline LLC

Reason
Failed Release Testing: Coarse Particle Mass for umeclidinium Out of Specification
Published
January 3, 2024
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

Odor-Eaters Spray Powder, Tolnaftate 1% Antifungal, packaged in a) 4 oz. aerosol cans (UPC 0 41388 0041 2, NDC 10157-4645-1) and b) 5.3 oz. aerosol cans (UPC 0 41388 00411 2, NDC 10157-4645-2) Blistex P.O. Box 5392, Oak Brook, IL 60522-5392.

by Blistex Inc

Reason
Chemical contamination: Presence of benzene
Published
December 27, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

Phenytoin Oral Suspension, USP, 100 mg/4 mL, packaged in packaged in 4 mL unit dose cups (NDC 0904-7079-24), 50 per case (NDC 0904-7079-57), Rx only, Major Pharmaceuticals Livonia, MI 48152

by The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Reason
Failed Content Uniformity Specifications
Published
December 27, 2023
Distribution
Nationwide

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FDA Recall Completed Historical recordClass I

TING 2% Miconazole Nitrate Athlete's Foot Spray Antifungal Spray Powder, NET WT 4.5 oz (128 g) cans, Distributed by: Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company, Tarrytown, NY 10591, UPC 363736532611.

by Insight Pharmaceuticals Corporation

Reason
Chemical Contamination; presence of benzene.
Published
December 27, 2023
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

The HMC Group Marketing Inc

Product
HMC Farms White Peaches 4lb box
Reason
Potential contamination with Listeria monocytogenes
Published
December 27, 2023
Distribution
U.S. distribution to the following: CA,…

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FDA Recall United States Terminated Historical recordClass I

The HMC Group Marketing Inc

Product
HMC Farms White Nectarines 4lb box
Reason
Potential contamination with Listeria monocytogenes
Published
December 27, 2023
Distribution
U.S. distribution to the following: CA,…

View recall →

FDA Recall United States Terminated Historical recordClass I

The HMC Group Marketing Inc

Product
HMC Farms Peaches 4lb box
Reason
Potential contamination with Listeria monocytogenes
Published
December 27, 2023
Distribution
U.S. distribution to the following: CA,…

View recall →

FDA Recall United States Terminated Historical recordClass I

The HMC Group Marketing Inc

Product
HMC Farms Nectarines 4lb bag
Reason
Potential contamination with Listeria monocytogenes
Published
December 27, 2023
Distribution
U.S. distribution to the following: CA,…

View recall →

FDA Recall United States Terminated Historical recordClass I

The HMC Group Marketing Inc

Product
HMC Farms Nectarines Signature Farms 2lb bag
Reason
Potential contamination with Listeria monocytogenes
Published
December 27, 2023
Distribution
U.S. distribution to the following: CA,…

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FDA Recall United States Terminated Historical recordClass I

The HMC Group Marketing Inc

Product
HMC Farms Peaches Signature Farms 2lb bag
Reason
Potential contamination with Listeria monocytogenes
Published
December 27, 2023
Distribution
U.S. distribution to the following: CA,…

View recall →

FDA Recall United States Terminated Historical recordClass I

The HMC Group Marketing Inc

Product
HMC Farms White Nectarines 2lb Gusset Bag
Reason
Potential contamination with Listeria monocytogenes
Published
December 27, 2023
Distribution
U.S. distribution to the following: CA,…

View recall →

FDA Recall United States Terminated Historical recordClass I

The HMC Group Marketing Inc

Product
HMC Farms White Peaches 2lb Gusset Bag
Reason
Potential contamination with Listeria monocytogenes
Published
December 27, 2023
Distribution
U.S. distribution to the following: CA,…

View recall →

FDA Recall United States Terminated Historical recordClass I

The HMC Group Marketing Inc

Product
HMC Farms Plums 2lb Gusset Bag
Reason
Potential contamination with Listeria monocytogenes
Published
December 27, 2023
Distribution
U.S. distribution to the following: CA,…

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.