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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 November 2026.

37,449
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,872
Class I recallsReasonable probability of serious health consequences
24,509
Class II recallsTemporary or medically reversible health consequences
2,932
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 2,096 recalls
Newest recallhttps://www.fsis.usda.gov/recalls-alerts/fsis-issues-public-health-alert-meat-and-poultry-products-due-misbranding-andPublished November 6, 2026
Most affected stateHawaii 200 recalls mention this state

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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)

  • 1,956 recalls have been announced year to date.
  • Oct 2026 was 4% higher than the previous complete period (Sep 2026: 209).
  • The highest complete period was Jun 2026 (300).
  • Nov 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 II24,509
Class I9,872
Class III2,932
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,509
Class I9,872
Class III2,932
Not Yet Classified2

Showing 12,681–12,700 of 21,307 recalls

FDA Recall TerminatedTerminated: January 20, 2021Historical 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 TerminatedTerminated: January 20, 2021Historical 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 TerminatedTerminated: January 20, 2021Historical 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 TerminatedTerminated: January 20, 2021Historical 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 TerminatedTerminated: January 20, 2021Historical 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 TerminatedTerminated: January 20, 2021Historical 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 TerminatedTerminated: January 20, 2021Historical 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 TerminatedTerminated: January 20, 2021Historical 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 OngoingHistorical 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 TerminatedTerminated: June 4, 2018Historical recordClass I

Cheezwhse/Com

Product
Formagere de la Brie brand, l 'Explorateur, soft ripened che…
Reason
Product may be contaminated with Listeria monocytogenes.
Published
May 2, 2018
Distribution
NY, NJ, CT, MD, UT, CO, SC, PA, TX and W…

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FDA Recall United States TerminatedTerminated: January 22, 2020Historical 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 TerminatedTerminated: April 5, 2019Historical 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 TerminatedTerminated: April 5, 2019Historical 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 TerminatedTerminated: April 5, 2019Historical 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 TerminatedTerminated: April 5, 2019Historical 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 TerminatedTerminated: April 5, 2019Historical 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 TerminatedTerminated: April 5, 2019Historical 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 TerminatedTerminated: September 10, 2018Historical 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 TerminatedTerminated: September 10, 2018Historical 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 →

FDA Recall TerminatedTerminated: January 14, 2019Historical recordClass II

ACURE, clarifying acne, glycolic + zinc (salicyclic acid 0.5%) towelettes, 30-count pouch, Distributed by Better Planet Brands, Fort Lauderdale, FL 33316, UPC 8 54049 00358 0.

by Diamond Wipes International, Inc.

Reason
CGMP Deviations: finished products were manufactured with poor quality water.
Published
April 25, 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.

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