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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.

37,142
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
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 II24,349
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 13,141–13,160 of 19,206 recalls

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,…

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FDA Recall United States Ongoing Historical recordClass I

MDS Foods Inc

Product
Colby Cheese packaged as follows: (a) AMISH CLASSICS, DELI…
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 Terminated Historical recordClass I

Dolce Dolci LLC dba Villa Dolce Gelato

Product
Strawberry Sorbet, 5 Liter, 1 unit/case
Reason
Villa Dolce Gelato is recalling Strawberry Gelato and Strawberry Sorbetto because they have the potential to be contaminated with hepatitis A virus.
Published
March 29, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Dolce Dolci LLC dba Villa Dolce Gelato

Product
Strawberry Gelato, 5 Liter, 1 unit/case
Reason
Villa Dolce Gelato is recalling Strawberry Gelato and Strawberry Sorbetto because they have the potential to be contaminated with hepatitis A virus.
Published
March 29, 2017
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

Lakeview Cheese Co Llc

Product
Cheddar Longhorn, 4/13# under Lakeview brand and LH Cheddar…
Reason
Firm was notified by supplier that cheese supplied to Lakeview from September 1, 2016 through January 27, 2017 is being recalled due to the potential of Listeria monocytogenes. contamination.
Published
March 29, 2017
Distribution
AZ, CA, UT, NV, WA, OR.

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FDA Recall United States Terminated Historical recordClass I

Lakeview Cheese Co Llc

Product
Food City random weight cut Pepper Jack Cheese., Also sold…
Reason
Firm was notified by supplier that cheese supplied to Lakeview from September 1, 2016 through January 27, 2017 is being recalled due to the potential of Listeria monocytogenes. contamination.
Published
March 29, 2017
Distribution
AZ, CA, UT, NV, WA, OR.

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FDA Recall United States Terminated Historical recordClass I

Lakeview Cheese Co Llc

Product
Food City Colby Monterey Cheese, 12 oz. package. (Bashas'…
Reason
Firm was notified by supplier that cheese supplied to Lakeview from September 1, 2016 through January 27, 2017 is being recalled due to the potential of Listeria monocytogenes. contamination.
Published
March 29, 2017
Distribution
AZ, CA, UT, NV, WA, OR.

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.