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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.

37,143
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,799
Class I recallsReasonable probability of serious health consequences
24,349
Class II recallsTemporary or medically reversible health consequences
2,891
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/sierra-nevada-cheese-company-recalls-graziers-raw-milk-cheese-because-possible-health-riskPublished September 28, 2026
Most affected stateHawaii 200 recalls mention this state

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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)

  • 1,653 recalls have been announced year to date.
  • Sep 2026 was 31% lower than the previous complete period (Aug 2026: 182).
  • The highest complete period was Jun 2026 (297).
Recalls by class

A bar chart of the total number of recalls in this dataset by recall class.

Recalls by class
ClassRecalls
Class II24,349
Class I9,799
Class III2,891
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,349
Class I9,799
Class III2,891
Not Yet Classified1

Showing 13,281–13,300 of 19,372 recalls

FDA Recall United States Terminated Historical recordClass II

Grace Kennedy Foods USA LLC

Product
La Fe Papa Criollas Yellow Potato Net Wt. 14 oz. Distribute…
Reason
La Fe Papas Criollos may be contaminated with Listeria Monoctyogenes.
Published
April 5, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass III

Give and Go Prepared Foods Corp - Finch

Product
The Bakery Mini Pecan Tarts Part Platter NET WT 16x 16.2 OZ…
Reason
Dried weevil larvae may be present in the recalled products.
Published
April 5, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass III

Give and Go Prepared Foods Corp - Finch

Product
Two-Bite Pecan Tarts Party Platter 16 x 16.2 (460g) item num…
Reason
Dried weevil larvae may be present in the recalled products.
Published
April 5, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass III

Give and Go Prepared Foods Corp - Finch

Product
Two-Bite Turtle Brownie Party Platter 16 x 12.2 oz (346g) it…
Reason
Dried weevil larvae may be present in the recalled products.
Published
April 5, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass III

Give and Go Prepared Foods Corp - Finch

Product
Two-Bite Pecan Tart 9.2 oz (261g) item number 02023; NL Two-…
Reason
Dried weevil larvae may be present in the recalled products.
Published
April 5, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Bitterman and Sons

Product
Parmesan Truffle Salt. The product is packaged in glass tast…
Reason
Parmigiano Reggiano (Parmesan) cheese is declared, but milk is not listed on label.
Published
April 5, 2017
Distribution
distributed in AK, CA, CT, FL, IL, IN, K…

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FDA Recall Terminated Historical recordClass II

Desonide Ointment, 0.05%, NET WT 60 grams tubes, Rx only, E. FOUGERA & CO. A division of Fougera Pharmaceuticals Inc., Melville, New York 11747, NDC 0168-0309-60

by Fougera Pharmaceuticals Inc.

Reason
Labeling: Label Mixup; Unit boxes labeled as Desonide Ointment 0.05% may contain tubes of Desonide Ointment labeled as Ketoconazole Cream
Published
March 29, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Testosterone Cypionate Injection , USP, 200 mg/mL, 1 mL vial , For Intramuscular Use Only, Rx Only, Distributed by Sun Pharma Ind. Inc., NJ 08512, Manufactured by Sun Pharma Ind. Ltd. India, NDC 62756-015-40

by Sun Pharmaceutical Industries, Inc.

Reason
Presence of Particulate Matter
Published
March 29, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Famciclovir tablets, 500 mg, packaged in 30-count unit dose cartons, Rx only, Manufactured for: AvKARE, Inc., Pulaski, TN 38478, NDC 50268-307-13

by AVKARE Inc.

Reason
Failed impurities/ degradation specifications: Product was above specification for unknown impurities.
Published
March 29, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Quillivant XR (methylphenidate HCl) for extended-release oral suspension, 900 mg/180 mL (25mg/5mL), Rx Only, Distributed by: NextWave Pharmaceuticals, Inc. A subsidiary of Pfizer Inc, New York, NY 10017 Manufactured by: Tris Pharma, Inc., Monmouth Junction, NJ 08852 (NDC 24478-190-30).

by PFIZER INC

Reason
Failed Dissolution Specifications: Dissolution at 8 hour was out of specification at 12 month at 25 degree Celsius.
Published
March 29, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Quillivant XR (methylphenidate HCl) for extended-release oral suspension, 750 mg/150 mL (25mg/5mL), Rx Only, Distributed by: NextWave Pharmaceuticals, Inc. A subsidiary of Pfizer Inc, New York, NY 10017 Manufactured by: Tris Pharma, Inc., Monmouth Junction, NJ 08852 (NDC 24478-205-25).

by PFIZER INC

Reason
Failed Dissolution Specifications: Dissolution at 8 hour was out of specification at 12 month at 25 degree Celsius.
Published
March 29, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Quillivant XR (methylphenidate HCl) for extended-release oral suspension, 300 mg/60 mL (25mg/5mL), Rx Only, Distributed by: NextWave Pharmaceuticals, Inc. A subsidiary of Pfizer Inc, New York, NY 10017 Manufactured by: Tris Pharma, Inc., Monmouth Junction, NJ 08852 (NDC 24478-190-10).

by PFIZER INC

Reason
Failed Dissolution Specifications: Dissolution at 8 hour was out of specification at 12 month at 25 degree Celsius.
Published
March 29, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

ATENOLOL Tablets, USP, 50 mg, 30-count bottle, Rx only, Distributed by: The Kroger Co., 1014 Vine Street, Cincinnati, OH 45202; Manufactured for: Zydus Pharmaceuticals USA Inc., Pennington, NJ 08534; Packaged by: Legacy Pharmaceutical Packaging LLC, Earth City, MO 63045; NDC 68645-493-54.

by Legacy Pharmaceutical Packaging LLC

Reason
Presence of Foreign Tablets/Capsules: Customer complaint that a bottle of atenolol 50 mg Tablets USP contained a paroxetine 20 mg tablet.
Published
March 29, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

ATENOLOL Tablets, USP, 50 mg, packaged in a) 100-count bottles (NDC 68382-023-01) and b) 1000-count bottles (NDC 68382-023-10), Rx only, Manufactured by: Cadila Healthcare Ltd., India; Distributed by: Zydus Pharmaceuticals USA Inc., Pennington, NJ 08534.

by Zydus Pharmaceuticals USA Inc

Reason
Presence of Foreign Tablets/Capsules: Customer complaint that a bottle of atenolol 50 mg Tablets USP contained a paroxetine 20 mg tablet.
Published
March 29, 2017
Distribution
Nationwide

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FDA Recall United States Ongoing Historical recordClass I

MDS Foods Inc

Product
Jalapeno Cheese packaged as: (a) Deli Readi Jalapeno St…
Reason
Potential cross contamination from a of product collected by the State Department of Agriculture which tested positive for Listeria Monocytogenes
Published
March 29, 2017
Distribution
FL, GA, IL, IN, KS, KY, MA, MI, MO, MC,…

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FDA Recall United States Ongoing Historical recordClass I

MDS Foods Inc

Product
Cheddar Cheese packaged as: (a) AMISH CLASSICS Cheddar Mild…
Reason
Potential cross contamination from a of product collected by the State Department of Agriculture which tested positive for Listeria Monocytogenes
Published
March 29, 2017
Distribution
FL, GA, IL, IN, KS, KY, MA, MI, MO, MC,…

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FDA Recall United States Ongoing Historical recordClass I

MDS Foods Inc

Product
Marble Cheese packaged as: (a) Troyer Marble EW Halfmoon, I…
Reason
Sample of product collected by the State Department of Agriculture tested positive for Listeria Monocytogenes
Published
March 29, 2017
Distribution
FL, GA, IL, IN, KS, KY, MA, MI, MO, MC,…

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FDA Recall United States Ongoing Historical recordClass I

MDS Foods Inc

Product
Farmers Cheese packaged as: (a) AMISH CLASSICS Farmers Ch…
Reason
Sample of product collected by the State Department of Agriculture tested positive for Listeria Monocytogenes
Published
March 29, 2017
Distribution
FL, GA, IL, IN, KS, KY, MA, MI, MO, MC,…

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FDA Recall United States Ongoing Historical recordClass I

MDS Foods Inc

Product
Jalapeno Colby Jack Cheese packaged as: (a) AMISH CLASSIC…
Reason
Sample of product collected by the State Department of Agriculture tested positive for Listeria Monocytogenes
Published
March 29, 2017
Distribution
FL, GA, IL, IN, KS, KY, MA, MI, MO, MC,…

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FDA Recall United States Ongoing Historical recordClass I

MDS Foods Inc

Product
Hot Pepper Cheese packaged as: (a) AMISH CLASSICS Hot Pep…
Reason
Potential cross contamination from a sample of product collected by the State Department of Agriculture which tested positive for Listeria Monocytogenes
Published
March 29, 2017
Distribution
FL, GA, IL, IN, KS, KY, MA, MI, MO, MC,…

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.