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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.

37,066
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
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/whole-foods-market-issues-allergy-alert-undeclared-egg-cabricharme-cheesePublished September 11, 2026
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 2,821–2,840 of 20,481 recalls

FDA Recall Completed Historical recordClass II

Lurasidone Hydrochloride Tablets 120mg, Rx Only, 30 Tablets per bottle, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, Manufactured by: Sun Pharmaceutical Industries Ltd., Survey No. 259/15, Dadra-396 191(U.T. of D & NH), INDIA, NDC 47335-579-83.

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason
CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment.
Published
January 31, 2024
Distribution
Nationwide

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FDA Recall Completed Historical recordClass II

Lurasidone Hydrochloride Tablets 60mg, Rx Only, 30 Tablets per bottle, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, Manufactured by: Sun Pharmaceutical Industries Ltd., Survey No. 259/15, Dadra-396 191(U.T. of D & NH), INDIA, NDC 47335-639-83.

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason
CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment.
Published
January 31, 2024
Distribution
Nationwide

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FDA Recall Completed Historical recordClass II

Febuxostat Tablets 80 mg, Rx Only, 30 Tablets per bottle, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, Manufactured by: Sun Pharmaceutical Industries Ltd., Survey No. 259/15, Dadra-396 191, (U.T. of D & NH), INDIA, NDC 47335-722-83.

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason
CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment.
Published
January 31, 2024
Distribution
Nationwide

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FDA Recall Completed Historical recordClass II

Febuxostat Tablets 40mg, Rx Only, 30 Tablets per bottle, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, Manufactured by: Sun Pharmaceutical Industries Ltd., Survey No. 259/15, Dadra-396 191 (U.T. of D & NH), INDIA, NDC 47335-721-83.

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason
CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment.
Published
January 31, 2024
Distribution
Nationwide

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FDA Recall Completed Historical recordClass II

Cinacalcet Tablets 60mg, Rx Only, 30 Tablets per bottle, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, Manufactured by: Sun Pharmaceutical Industries Limited Survey No. 259/15, Dadra-396 191 (U.T. of D & NH), India, NDC 47335-380-83.

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason
CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment.
Published
January 31, 2024
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Fosaprepitant for Injection 150 mg per vial, Sterile lyophilized powder for Intravenous use only after reconstitution and dilution, Single Dose Vial, Rx Only, Distributed by BE Pharmaceuticals Inc. 203 New Edition Court Cary, NC 27511, Made in India, NDC 71839-104-01.

by BE PHARMACEUTICALS AG

Reason
Lack of Sterility Assurance: Aseptic process simulation failure.
Published
January 31, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass I

Bleomycin for Injection, USP, 15 units per vial, 1 single dose glass fliptop vial, Rx Only, Distributed by: Hospira, Inc., Lake Forest, IL 68045, NDC 61703-332-18

by Pfizer

Reason
Presence of particulate matter: glass
Published
January 31, 2024
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Methoxsalen Capsules, USP 10mg, 50-count bottle, Rx Only, Manufactured by: Strides Pharma Science Ltd. Bengaluru - 562106, India. Distributed by:Strides Pharma Inc. East Brunswick, NJ 08816, NDC 64380-752-16

by Strides Pharma Inc.

Reason
Failed Dissolution Specifications
Published
January 31, 2024
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Fluocinolone Acetonide Oil, 0.01% (Ear Drops), package in 1 Oz. (20 mL fill volume) bottle, Rx only, Manufactured by: Glenmark Pharmaceuticals Ltd., Village: Kishanpura, Baddi Nalagarh Road, District: Solan, Himachal Pradesh - 173205, India, Manufactured for: Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ 07430, NDC 68462-185-56

by Glenmark Pharmaceuticals Inc., USA

Reason
Failed Excipient Specifications: OOS for assay of Isopropyl Alcohol
Published
January 31, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass III

Benzonatate Capsules, USP, 100 mg, 100 Capsules (10 capsules x 10 unit dose cards), Rx only, Distributed by: American Health Packaging, Columbus, Ohio 43217. Carton NDC 68084-214-01; Individual Dose NDC 68084-214-11

by Amerisource Health Services LLC

Reason
Superpotent drug: Assay results were slightly above specification at the time zero point.
Published
January 31, 2024
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Lidl US TRADING

Product
Duc De Coeur Camembert Cheese Croquettes Frozen NET WT 9 OZ…
Reason
Possible contamination with Listeria monocytogenes
Published
January 31, 2024
Distribution
Distribution centers and retails stores…

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FDA Recall United States Terminated Historical recordClass II

Stonewall Kitchen, LLC

Product
Vermont Village Unsweetened Apple Sauce (24oz)
Reason
Product contains elevated levels of patulin.
Published
January 31, 2024
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass II

Lecoq Cuisine Corporation

Product
RTB MIXED DANISH Variety
Reason
Contains undeclared soy lecithin.
Published
January 31, 2024
Distribution
Arizona, California, Colorado, Connectic…

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FDA Recall United States Terminated Historical recordClass II

Lecoq Cuisine Corporation

Product
R&B Chocolate Chips Croissant Twist
Reason
Contains undeclared soy lecithin.
Published
January 31, 2024
Distribution
Arizona, California, Colorado, Connectic…

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FDA Recall United States Terminated Historical recordClass I

Publix Super Markets, Inc.

Product
Publix Self Service Salad from the Salad Bar, variable weigh…
Reason
The underlying ingredient, shredded lettuce, was recalled by the supplier Fresh Express due to potential contamination with Listeria monocytogenes.
Published
January 31, 2024
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

Publix Super Markets, Inc.

Product
Publix Custom Made Platters, variable weights and sizes, pac…
Reason
The underlying ingredient, shredded lettuce, was recalled by the supplier Fresh Express due to potential contamination with Listeria monocytogenes.
Published
January 31, 2024
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

Publix Super Markets, Inc.

Product
Publix Deli Chicken Street Tacos for Two, variable weights a…
Reason
The underlying ingredient, shredded lettuce, was recalled by the supplier Fresh Express due to potential contamination with Listeria monocytogenes.
Published
January 31, 2024
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

Publix Super Markets, Inc.

Product
Publix Custom Burrito Bowls, variable weights and sizes, pac…
Reason
The underlying ingredient, shredded lettuce, was recalled by the supplier Fresh Express due to potential contamination with Listeria monocytogenes.
Published
January 31, 2024
Distribution
Multiple states

View recall →

FDA Recall United States Terminated Historical recordClass I

Publix Super Markets, Inc.

Product
Publix Custom Made Pizzas, variable weights and sizes, packe…
Reason
The underlying ingredient, shredded lettuce, was recalled by the supplier Fresh Express due to potential contamination with Listeria monocytogenes.
Published
January 31, 2024
Distribution
Multiple states

View recall →

FDA Recall United States Terminated Historical recordClass I

Publix Super Markets, Inc.

Product
Publix Custom Made Sub Sandwiches, variable weights and size…
Reason
The underlying ingredient, shredded lettuce, was recalled by the supplier Fresh Express due to potential contamination with Listeria monocytogenes.
Published
January 31, 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.