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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.

37,115
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,793
Class I recallsReasonable probability of serious health consequences
24,343
Class II recallsTemporary or medically reversible health consequences
2,887
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/so-delicious-dairy-freer-issues-voluntary-recall-salted-caramel-cluster-non-dairy-frozen-dessertPublished September 15, 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 II24,343
Class I9,793
Class III2,887
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,343
Class I9,793
Class III2,887
Not Yet Classified1

Showing 7,221–7,240 of 25,257 recalls

FDA Recall United States Terminated Historical recordClass I

Joonsung Trading Inc

Product
Spicy Chicken Sauce packaged in 1/2 gallon plastic jug. Lab…
Reason
Undeclared wheat. Label declares Hot Bean Paste but does not declared Wheat.
Published
June 1, 2022
Distribution
Distributed in Oregon and Washington

View recall →

FDA Recall United States Terminated Historical recordClass I

Joonsung Trading Inc

Product
Mio Salad Dressing packaged in 1 gallon plastic jug. Label…
Reason
Undeclared egg. Label declares Mayo but does not declare Egg.
Published
June 1, 2022
Distribution
Distributed in Oregon and Washington

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FDA Recall United States Terminated Historical recordClass I

Joonsung Trading Inc

Product
Chirashi Sauce packaged in 1/2 gallon plastic jug. Label re…
Reason
Undeclared soy and wheat. Label declares Hot Bean Paste but does not declare Soy and Wheat.
Published
June 1, 2022
Distribution
Distributed in Oregon and Washington

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FDA Recall United States Terminated Historical recordClass I

Joonsung Trading Inc

Product
Champon Soup Base packaged in 32 oz plastic jug. The label…
Reason
Undeclared milk and tuna. Label declares Hondashi but does not declare Milk and Tuna.
Published
June 1, 2022
Distribution
Distributed in Oregon and Washington

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FDA Recall Terminated Historical recordClass III

Sirolimus Oral Solution, 1 mg/mL, 60 mL bottle, Rx Only, Manufactured by: Apotex Inc. Toronto, Ontario Canada M9L 1T9 Manufactured for: Apotex Corp. Weston, Florida 33326, NDC 60505-6197-2

by Apotex Corp.

Reason
Failed Dissolution Specifications: Sirolimus Oral Solution recalled due to lot RZ1598 exceeded the specification limit at the 14-month timepoint.
Published
May 25, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Nitrofurantoin Capsules, USP (Monohydrate/Macrocrystals), 100 mg, 100 Capsules (10 x 10), 10-count blisters per card, 10 cards per carton, Unit Dose NDC 68084-446-11, Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217, NDC: 68084-446-01

by American Health Packaging

Reason
Failed Dissolution Specifications: Nitrofurantoin Capsules recalled due to dissolution failure at 0-time of the repackaged lot. Drug release results were above specification at 0-time.
Published
May 25, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

GaviLyte -C (Polyethylene Glycol 3350, 240 g) and electrolytes for Oral Solution, USP with flavor pack NDC# 43386-060-19

by Lupin Pharmaceuticals Inc.

Reason
Failed Stability Specification
Published
May 25, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Accupril (Quinapril HCl Tablets) 40 mg, 90 Tablets, Rx only NDC 0071-0535-23 Distributed by: Parke-Davis Division of Pfizer Inc. NY, NY 10017

by Pfizer Inc.

Reason
CGMP Deviations: Contains N-nitrosoquinapril above the acceptable limits.
Published
May 25, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Accupril (Quinapril HCl Tablets) 20 mg, 90 Tablets, Rx only NDC 0071-0532-23 Distributed by: Parke-Davis Division of Pfizer Inc. NY, NY 10017

by Pfizer Inc.

Reason
CGMP Deviations: Contains N-nitrosoquinapril above the acceptable limits.
Published
May 25, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Accupril (Quinapril HCl Tablets) 10 mg, 90 Tablets Rx only NDC 0071-0530-23 Distributed by: Parke-Davis Division of Pfizer Inc. NY, NY 10017

by Pfizer Inc.

Reason
CGMP Deviations: Contains N-nitrosoquinapril above the acceptable limits.
Published
May 25, 2022
Distribution
Nationwide

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FDA Recall Completed Historical recordClass II

Magnesium Hydroxide 1200mg, Aluminum Hydroxide 1200mg, Simethicone 120mg, 30 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Distributed by Major Pharmaceuticals, Livonia, MI 48152, NDC: 0904-6838-73.

by Plastikon Healthcare LLC

Reason
CGMP Deviations: Failure to properly investigate failed microbial testing.
Published
May 25, 2022
Distribution
Distributed in Indiana for further distr…

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FDA Recall Completed Historical recordClass II

MILK OF MAGNESIA USP, (Magnesium Hydroxide), 2400 mg/30 mL, 30 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Distributed by Major Pharmaceuticals, Livonia, MI 48152, NDC 0904-6846-73.

by Plastikon Healthcare LLC

Reason
CGMP Deviations: Failure to properly investigate failed microbial testing.
Published
May 25, 2022
Distribution
Distributed in Indiana for further distr…

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FDA Recall Completed Historical recordClass II

Acetaminophen Oral Solution, USP 650mg/ 20.3 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Distributed by Major Pharmaceuticals, Livonia, MI 48152, NDC: 0904-6820-76.

by Plastikon Healthcare LLC

Reason
CGMP Deviations: Failure to properly investigate failed microbial testing.
Published
May 25, 2022
Distribution
Distributed in Indiana for further distr…

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FDA Recall Completed Historical recordClass I

Magnesium Hydroxide 1200mg, Aluminum Hydroxide 1200mg, Simethicone 120mg, 30 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Distribute by Major Pharmaceuticals, Livonia, MI 48152, NDC: 0904-6838-73.

by Plastikon Healthcare LLC

Reason
Microbial Contamination of Non-Sterile Products
Published
May 25, 2022
Distribution
Distributed in Indiana for further distr…

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FDA Recall Completed Historical recordClass I

MILK OF MAGNESIA USP, (Magnesium Hydroxide), 2400 mg/30 mL, 30 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Distributed by Major Pharmaceuticals, Livonia, MI 48152, NDC 0904-6846-73.

by Plastikon Healthcare LLC

Reason
Microbial Contamination of Non-Sterile Products
Published
May 25, 2022
Distribution
Distributed in Indiana for further distr…

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FDA Recall United States Terminated Historical recordClass III

Driscoll's Inc.

Product
Driscoll's Blackberries (Fresh) 12x6 oz, 12x12 oz, 12x10 oz…
Reason
California Department of Pesticide Regulation detected the presence of Formetante HCI. This pesticide has a non-tolerance for blackberries.
Published
May 25, 2022
Distribution
Product shipped to 13 DC's located in CA…

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FDA Recall United States Terminated Historical recordClass III

R & S Roberts Enterprises, Inc.

Product
Milk & Dark Chocolate Sea Salt Healthy Bites. Chocolate coa…
Reason
Undeclared Soy Lecithin. Firm used Canola Oil spray as a releasing agent but finished products labels do not declare Soy Lecithin.
Published
May 25, 2022
Distribution
Distributed in Washington.

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FDA Recall United States Terminated Historical recordClass III

R & S Roberts Enterprises, Inc.

Product
Milk & Dark Chocolate Healthy Bites. Chocolate coated cara…
Reason
Undeclared Soy Lecithin. Firm used Canola Oil spray as a releasing agent but finished products labels do not declare Soy Lecithin.
Published
May 25, 2022
Distribution
Distributed in Washington.

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FDA Recall United States Terminated Historical recordClass III

R & S Roberts Enterprises, Inc.

Product
Milk & Dark Chocolate Caramel Macchiato. Chocolate coated c…
Reason
Undeclared Soy Lecithin. Firm used Canola Oil spray as a releasing agent but finished products labels do not declare Soy Lecithin.
Published
May 25, 2022
Distribution
Distributed in Washington.

View recall →

FDA Recall United States Terminated Historical recordClass III

R & S Roberts Enterprises, Inc.

Product
Milk & Dark Chocolate Sea Salt Caramels. Chocolate coated c…
Reason
Undeclared Soy Lecithin. Firm used Canola Oil spray as a releasing agent but finished products labels do not declare Soy Lecithin.
Published
May 25, 2022
Distribution
Distributed in Washington.

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.