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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.

37,063
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,786
Class I recallsReasonable probability of serious health consequences
24,313
Class II recallsTemporary or medically reversible health consequences
2,876
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/evergreen-fresh-sprouts-llc-recalls-broccoli-sprouts-because-possible-health-riskPublished September 10, 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 II24,313
Class I9,786
Class III2,876
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,313
Class I9,786
Class III2,876
Not Yet Classified2

Showing 2,341–2,360 of 17,993 recalls

FDA Recall Terminated Historical recordClass III

Digoxin Tablets, USP 125mcg, (0.125 mg), 1000-count bottle, Rx Only, Manufactured by: Novitium Pharma LLC., 70 Lake Drive, East Windsor, New Jersey 08520, NDC 70954-201-20

by Novitium Pharma LLC

Reason
Cross Contamination with Other Products:(mycophenolate mofetil).
Published
March 27, 2024
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Telmisartan Tablets, USP 40mg, Rx Only, 30 Tablets per bottle, Manufactured by: Micro Labs Limited Goa-403 722, INDIA, Manufactured for: Micro Labs USA Inc., Somerset, NJ 08873, NDC 42571-227-30.

by Micro Labs Limited

Reason
Failed Stability Specifications: Out of specification for blend uniformity.
Published
March 20, 2024
Distribution
Puerto Rico, TN, RI

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FDA Recall Ongoing Historical recordClass II

Broncochem Cold & Tea (acetaminophen, phenylephrine, HCl, chlorpheniramine maleate), packaged in 13g sachets, 25 sachets per box, Made in the Dominican Republic Exclusively for Global Corporation Inc, Boca Raton, FL 33187 USA, NDC 65131-097-12

by Global Corporation

Reason
Stability testing failures for one or two of the four active pharmaceutical ingredients among the finished drug products, i.e., Phenylephrine HCL, and/or Chlorpheniramine Maleate.
Published
March 20, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Broncochem Cold & Flu Syrup Kids (acetaminophen, guaifenesin, phenylephrine HCl), packaged in 120 mL bottles, Made in Dominican Republic Exclusively for Global Corporation Inc, Boca Raton, FL 33187 USA, NDC 65131-098-44

by Global Corporation

Reason
Stability testing failures for one or two of the four active pharmaceutical ingredients among the finished drug products, i.e., Phenylephrine HCL, and/or Chlorpheniramine Maleate.
Published
March 20, 2024
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Tobramycin for Injection, USP, 1.2 grams per Pharmacy Bulk Package, Rx Only, For Intravenous Use, PHARMACY BULK PACKAGE NOT FOR DIRECT INFUSION, Mfd. in India for: Eugia US LLC, E. Windsor, NJ 08520, Carton NDC 55150-470-06, Vial NDC 55150-470-01.

by Eugia US LLC

Reason
Failed Stability Specification: Water determination was found not complying with specification.
Published
March 20, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

hyalogic For Dry Eyes, HylaTears", Lubricant Eye Drops, 0.67 FL OZ (20mL) bottle, Manufactured for hyalogic, 610 NW Platte Valley Dr., Riverside, MO 64150

by Optikem International, Inc.

Reason
Lack of Assurance of Sterility
Published
March 20, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

TRP Natural Eyes Red Eye Relief, Sterile Eye Drops, Homeopathic, 0.33 FL OZ (10 mL), Manufactured for TRP Company, Inc, 1575 Delucchi Lane, Suite # 208, Reno, NV, NDC # 17312-158-15.

by Optikem International, Inc.

Reason
Lack of Assurance of Sterility
Published
March 20, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

TRP Natural Eyes Pink Eye Relief, Sterile Eye Drops, Homeopathic, 0.33 FL OZ (10 mL), Manufactured for TRP Company, Inc, 1575 Delucchi Lane, Suite # 208, Reno, NV, NDC # 17312-013-15.

by Optikem International, Inc.

Reason
Lack of Assurance of Sterility
Published
March 20, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

TRP Natural Eyes Aging Eye Relief, Sterile Eye Drops, Homeopathic, 0.33 FL OZ (10 mL), Manufactured for TRP Company, Inc, 1575 Delucchi Lane, Suite # 208, Reno, NV, NDC # 17312-027-15.

by Optikem International, Inc.

Reason
Lack of Assurance of Sterility
Published
March 20, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

TRP Natural Eyes Floaters Relief, Sterile Eye Drops, 0.33 FL OZ (10 mL), Manufactured for TRP Company, Inc, 1575 Delucchi Lane, Suite # 208, Reno, NV, NDC # 17312-098-15.

by Optikem International, Inc.

Reason
Lack of Assurance of Sterility
Published
March 20, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

TRP Eye strain Relief, Sterile Eye Drops, Homeopathic, 0.33 FL OZ (10 mL), Manufactured for TRP Company, Inc, 1575 Delucchi Lane, Suite # 208, Reno, NV, NDC # 17312-172-15.

by Optikem International, Inc.

Reason
Lack of Assurance of Sterility
Published
March 20, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

TRP Natural Eyes Dryness Relief, Sterile Eye Drops, 0.33 FL OZ (10 mL), Manufactured for TRP Company, Inc, 1575 Delucchi Lane, Suite # 208, Reno, NV, NDC # 17312-178-15.

by Optikem International, Inc.

Reason
Lack of Assurance of Sterility
Published
March 20, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

TRP Eye Twitching Relief, Sterile Eye Drops, Homeopathic 0.33 FL OZ (10 mL), Manufactured for TRP Company, Inc, 1575 Delucchi Lane, Suite # 208, Reno, NV, NDC # 17312-040-15.

by Optikem International, Inc.

Reason
Lack of Assurance of Sterility
Published
March 20, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

TRP Blur Relief, Sterile Eye Drops, Homeopathic 0.5 FL OZ (15mL), Manufactured for TRP Company, Inc, 1575 Delucchi Lane, Suite # 208, Reno, NV, NDC # 17312-002-11.

by Optikem International, Inc.

Reason
Lack of Assurance of Sterility
Published
March 20, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

TRP Natural Eyes Allergy Eyes Relief, Sterile Eye Drops, Homeopathic 0.33 FL OZ (10mL), Manufactured for TRP Company, Inc, 1575 Delucchi Lane, Suite # 208, Reno, NV, NDC # 17312-032-15.

by Optikem International, Inc.

Reason
Lack of Assurance of Sterility
Published
March 20, 2024
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Betimol (timolol ophthalmic solution) 0.5%, 15mL bottles, Rx only, Manufactured for: Thea Pharma Inc. Lexington, MA 02420, NDC 82584-002-15

by Thea Pharma, Inc.

Reason
Lack of Assurance of Sterility: Out of specification for volume and compromised container closure.
Published
March 20, 2024
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Potassium Chloride for Injection Concentrate USP, 500 mEq/250 mL (2 mEq/mL), 250 mL Bag, Rx only, B. Braun Medical Inc., Bethlehem, PA 18018, NDC 0264-1944-20

by B. Braun Medical Inc

Reason
Lack of assurance of sterility: pinholes, within the blue label characters on the EXCEL bag, specifically within the dotted characters on the label, resulting in leaks.
Published
March 20, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Febuxostat Tablets 80mg, RX Only, 30 Tablets per bottle, NorthStarx, Manufactured for: Northstar Rx LLC., Memphis, TN 38141, Manufactured by: Sun Pharmaceutical Industries Limited Survey No. 259/15, Dadra-396 191, (U.T. of D & NH), India, NDC 16714-060-01.

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason
CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment.
Published
March 20, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Febuxostat Tablets 40mg, RX Only, 30 Tablets per bottle, NorthStarx, Manufactured for: Northstar Rx LLC., Memphis, TN 38141 , Manufactured by: Sun Pharmaceutical Industries Limited Survey No. 259/15, Dadra-396 191, (U.T. of D & NH), India, NDC 16714-059-01.

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason
CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment.
Published
March 20, 2024
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Trader Joe's Company

Product
Trader Joe s Southwest Salad (SKU 56077) 9 oz.
Reason
L. mono contamination
Published
March 20, 2024
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.