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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 2,621–2,640 of 18,346 recalls

FDA Recall Terminated Historical recordClass II

Doxycycline Capsules, USP 100 mg, 50 Capsules, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, Maryland 21202 Unite States; Manufactured by: Lupin Limited, Nagpur - 441 108, INDIA. NDC 68180-652-08

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

Donepezil HCl Tablets, 5 mg, 90 Tablets, Rx only, Distributed by: Solco Healthcare U.S. LLC, Hurracao, Puerto Rico 00791. NDC: 43547-275-09

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

Donepezil HCl Tablets, 10 mg, 90 Tablets, Rx only, Distributed by: Solco Healthcare U.S. LLC, Hurracao, Puerto Rico 00791. NDC: 43547-276-09

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

Dicyclomine Hydrochloride Tablets, USP 20 mg, 100 Tablets, Rx only, Manufactured For: Teva Pharmaceuticals USA, Parsippany, NJ 07054. NDC: 0591-0795-01

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

Colgate Total SF Toothpaste, Net Wt 4.8 oz (136 g), Stannous Fluoride 0.454%, Clean Mint, Dist. by: COLGATE-PALMOLIVE CO., New York, NY 10022 USA

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

CITALOPRAM Tablets, USP, 20MG, 100 Tablets, Rx only, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 USA. NDC: 0378-6232-01

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

CHLORTHALIDONE Tablets, USP, 25MG, 1000 Tablets, Rx only, Manufactured by: Appco Pharma LLC, Piscataway, NJ 08854 USA; Manufactured For: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540 USA. NDC: 43598-719-10

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

Bumetanide Tablets, USP, 2 mg, 100 Tablets per bottle, Rx only, Manufactured by: Amneal Pharmaceuticals Pvt. Ltd., Ahmedabad 382213 India; Distributed by: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807

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

Low Dose ASPIRIN, 81 mg, 120 Enteric Coated Tablets, Distributed by: Rugby Lavoratories, 17177 N Laurel Park Drive, Suite 233, Livonia, MI 48152. NDC: 0536-1234-41

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

Asmanex Twisthaler (mometasone furoate inhalation powder, 220 mcg per actuation), 120 Metered Doses, Rx only, Manufactured for: Organon LLC, a subsidiary of Organon & Co., Jersey City, NJ 07302; Manufactured by: MSD International GmbH (Singapore Branch) Singapore 638030, Singapore. NDC: 78206-114-01

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

ARMOUR THYROID (thyroid tablets, USP), 2 GRAIN (120 mg), 100 Tablets, Rx Only, Distributed by: Allergan US, INc., Madison, NJ 07940. NDC: 0456-0461-01

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

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

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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

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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

View recall →

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

View recall →

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 United States Terminated Historical recordClass III

Wakefern Foods Corp.

Product
Bowl & Basket Zero Calorie with Sucralose Sweetener 100 coun…
Reason
Undeclared aspartame lack of phenylalanine warning
Published
January 3, 2024
Distribution
Multiple states

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.