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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.

37,139
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/deanos-pasta-issue-allergy-alert-undeclared-lobster-pear-and-pecorino-triangoli-ravioliPublished September 24, 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 II24,349
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 10,701–10,720 of 18,726 recalls

FDA Recall Terminated Historical recordClass II

Ibuprofen Caplets USP 200 mg, a) 50 caplets (NDC 49483-600-05), b) 100 caplets (NDC 49483-600-01), c) 500 caplets (NDC 49483-600-50), and d) BULK (NDC 49483-600-00) bottles, Rx, Manufactured for: Time Cap labs, Inc., Farmingdale, NY 11735, Manufactured by: Marksans Pharma, Ltd., Verna, Goa-403 722, India

by Time-Cap Laboratories, Inc.

Reason
CGMP Deviations: Various strengths of ibuprofen tablets/caplets are being recalled due to complaints of odor related to CGMP deficiencies.
Published
May 2, 2018
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Ibuprofen Tablets USP 800 mg, a) 100 tablet (NDC 42582-113-10) and b) 500 tablet (NDC 42582-113-18) bottles, Rx, Distributed by; Bi-Coastal Pharma International, Shrewsbury, NJ, Manufactured by: Marksans Pharma, Ltd., Verna, Goa-403 722, India

by Time-Cap Laboratories, Inc.

Reason
CGMP Deviations: Various strengths of ibuprofen tablets/caplets are being recalled due to complaints of odor related to CGMP deficiencies.
Published
May 2, 2018
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Ibuprofen Tablets USP 800 mg, a) 100 tablet (NDC 49483-604-01) and b) 500 tablet (NDC 49483-604-50) bottles, Rx, Manufactured for: Time Cap labs, Inc., Farmingdale, NY 11735, USA, Manufactured by: Marksans Pharma, Ltd., Verna, Goa-403 722, India

by Time-Cap Laboratories, Inc.

Reason
CGMP Deviations: Various strengths of ibuprofen tablets/caplets are being recalled due to complaints of odor related to CGMP deficiencies.
Published
May 2, 2018
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Ibuprofen Tablets USP 600 mg, a) 100 tablet (NDC 42582-112-01), b) 500 tablet bottles (NDC 42582-112-18), Rx, Distributed by Drug Mart, Food Fair, Medina, Ohio 44256

by Time-Cap Laboratories, Inc.

Reason
CGMP Deviations: Various strengths of ibuprofen tablets/caplets are being recalled due to complaints of odor related to CGMP deficiencies.
Published
May 2, 2018
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Ibuprofen Tablets USP 600 mg, a) 100 tablets (NDC 42582-112-10) and b) 500 tablet bottles (NDC 42582-112-18), Rx, Distributed by: Bi-Coastal Pharma International, Shrewsbury, NJ, Manufactured by: Marksans Pharma, Ltd., Plot No. L-82, L-83 Verna indl. Estate Verna, Goa-403 722, India

by Time-Cap Laboratories, Inc.

Reason
CGMP Deviations: Various strengths of ibuprofen tablets/caplets are being recalled due to complaints of odor related to CGMP deficiencies.
Published
May 2, 2018
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Ibuprofen Tablets USP 600 mg, a) 100 tablet (NDC 49483-603-01) and b) 500 tablet bottles (NDC 49483-603-50), Rx, Manufactured for: Time Caps Labs, Farmingdale, NY, Manufactured by: Marksans Pharma, Ltd., Plot No. L-82, L-83 Verna indl. Estate Verna, Goa-403 722, India

by Time-Cap Laboratories, Inc.

Reason
CGMP Deviations: Various strengths of ibuprofen tablets/caplets are being recalled due to complaints of odor related to CGMP deficiencies.
Published
May 2, 2018
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Ibuprofen Tablets USP 400 mg, 500 tablet bottles (NDC 42582-111-18), Rx, Distributed by Bi-Coastal Pharma International, Shrewsbury, NJ, Manufactured by: Marksans Pharma, Ltd., Plot No. L-82, L-83 Verna indl. Estate Verna, Goa-403 722, India

by Time-Cap Laboratories, Inc.

Reason
CGMP Deviations: Various strengths of ibuprofen tablets/caplets are being recalled due to complaints of odor related to CGMP deficiencies.
Published
May 2, 2018
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Ibuprofen Tablets USP 400 mg, a) 100 tablet (NDC 49483-602-01) and b) 500 tablet (NDC 49483-602-50) bottles, Rx, Manufactured for: Time Cap labs, Inc., Farmingdale, NY 11735, USA, Manufactured by: Marksans Pharma, Ltd., Plot No. L-82, L-83 Verna indl. Estate Verna, Goa-403 722, India

by Time-Cap Laboratories, Inc.

Reason
CGMP Deviations: Various strengths of ibuprofen tablets/caplets are being recalled due to complaints of odor related to CGMP deficiencies.
Published
May 2, 2018
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Ibuprofen Tablets, USP, 200 mg, a) 50 tablet (NDC 53943-291-15), b) 100 tablet (NDC 53943-291-12), c) 500 tablet (NDC 53943-291-14), Brown, Distributed by Drug Mart, Food Fair, Medina, Ohio 44256

by Time-Cap Laboratories, Inc.

Reason
CGMP Deviations: Various strengths of ibuprofen tablets/caplets are being recalled due to complaints of odor related to CGMP deficiencies.
Published
May 2, 2018
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Ibuprofen Tablets, USP, 200 mg, a) 50 tablets (NDC 49483-601-05), b) 100 tablets (NDC- 49483-601-01), c) 500 tablets (NDC 49483-601-50), d) 1000 tablets (NDC 49489-601-10), e) Bulk (49483-601-00) bottles, Brown, Manufactured for: Time Cap Labs, Inc., Farmingdale, NY 11735, Manufactured by: Marksans Pharma, Ltd., Verna, Goa-403 722, India

by Time-Cap Laboratories, Inc.

Reason
CGMP Deviations: Various strengths of ibuprofen tablets/caplets are being recalled due to complaints of odor related to CGMP deficiencies.
Published
May 2, 2018
Distribution
Nationwide

View recall →

FDA Recall United States Ongoing Historical recordClass I

ROSE ACRE FARM

Product
Shell Eggs packaged in quantities and styles of pack (plasti…
Reason
Shell eggs have the potential to be contaminated with Salmonella Braenderup.
Published
May 2, 2018
Distribution
Direct consignees located in MS, NJ, GA,…

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FDA Recall United States Terminated Historical recordClass I

NGB, Corp

Product
Nxtgen Botanicals, Maeng Da Kratom, Dietary Supplement, 70 c…
Reason
NGB Corp is recalling Nxtgen Botanicals due to potential Salmonella contamination.
Published
May 2, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Maharaja Food Importers, Inc.

Product
WHOLE WHEAT PAROTTA, UPC: 8 70400 00092 0
Reason
Label states ghee, but does not declare milk.
Published
May 2, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Maharaja Food Importers, Inc.

Product
MMRF Ela Ada Jaggery, UPC: 870400000067, Frozen
Reason
Label states ghee, but does not declare milk.
Published
May 2, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Maharaja Food Importers, Inc.

Product
Parotta Family Pack, UPC: 8 70400 00084 5, Frozen; and Small…
Reason
Label states ghee, but does not declare milk.
Published
May 2, 2018
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Maharaja Food Importers, Inc.

Product
MMRF Neyyappam, UPC: 870400000111, Frozen
Reason
Label states ghee, but does not declare milk.
Published
May 2, 2018
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Maharaja Food Importers, Inc.

Product
MMRF Kumbiliappam, UPC: 87040000104, Frozen
Reason
Label states ghee, but does not declare milk.
Published
May 2, 2018
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Maharaja Food Importers, Inc.

Product
ELA ADA (JACK FRUIT), UPC: 8 70400 00085 2
Reason
Label states ghee, but does not declare milk.
Published
May 2, 2018
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

Seabear Company

Product
Cold Smoked Wild Coho Salmon Lox , Gerard & Dominique Seafoo…
Reason
Products recalled due to water phase salt deviations and mislabeling of storage instructions on finished products labels
Published
May 2, 2018
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

Seabear Company

Product
Hot Smoked Keta Beergarden Salmon, Seabear brand, Reduced Ox…
Reason
Products recalled due to water phase salt deviations and mislabeling of storage instructions on finished products labels
Published
May 2, 2018
Distribution
Nationwide

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.