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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 17,805 recalls

FDA Recall Terminated Historical recordClass II

fentaNYL 2,500 mcg/50 mL Injection (Concentration = 50 mcg/mL), INTRAVENOUS USE ONLY, 50 mL Bag, Rx only, SCA Pharma, 755 Rainbow Rd., Windsor, CT 06095, NDC 70004-0222-30 BAR code 70004022230

by SCA Pharmaceuticals, LLC

Reason
Lack of Assurance of Sterility
Published
April 3, 2024
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

fentaNYL 2,500 mcg/250 mL in 0.9% Sodium Chloride Injection (Concentration = 10 mcg/mL), 250 mL Bag, Rx only, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT 06095, 877.550.5059, NDC 70004-0229-40 BAR code 70004022940

by SCA Pharmaceuticals, LLC

Reason
Lack of Assurance of Sterility
Published
April 3, 2024
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Diltiazem HCl 125 mg in 0.9% Sodium Chloride Injection (Concentration = 1mg/mL), 125 mL Bag, Rx only, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT 06095; NDC 70004-0541-35, Bar Code 70004054135

by SCA Pharmaceuticals, LLC

Reason
Lack of Assurance of Sterility
Published
April 3, 2024
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

WS Global Inc

Product
Himalayan Pain Relief Tea for Gout and Hangover
Reason
Contains undeclared drugs Diclofenac and Dexamethasone Acetate
Published
April 3, 2024
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

Neptune's Fix, Tianeptine Elixir, Fast Acting, 0.338 fl.oz. (10 mL) bottle, Distributed By Superchill Products, 827 6th Avenue, New York, New York 10001.

by Super Chill Products

Reason
Marketed without an approved NDA/ANDA: Product contains tianeptine, a substance not FDA-approved for any medical use in the United States.
Published
March 27, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Infumorph (Preservative-free Morphine Sulfate Sterile Solution), 20 mL ampul, Rx only, Manufactured by Hikma Berkeley Heights, NJ 07922, NDC 0641-6039-01

by Hikma Pharmaceuticals USA Inc.

Reason
The filter included in the carton has an expiration date that has expired prior to the expiration date of the actual product lot.
Published
March 27, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Nicardipine Hydrochloride Injection, USP 25mg/mL (2.5 mg/mL) 10 mL vials, Distributed by: AuroMedics Pharma LLC 279 Princeton-Hightstown Rd. E. Windsor, NJ 08520, NDC 55150-183-11

by Eugia US LLC

Reason
Failed Impurities/Degradation Specifications: Out of specification for organic impurities
Published
March 27, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Nicardipine Hydrochloride Injection (2.5mg/mL), US, 25mg per 10mL, 10mL Vial, Rx only, Distributed by: AuroMedics Pharma LLC 279 Princeton-Hightstown Rd. E. Windsor, NJ 08520 NDC 55150-183-10

by Eugia US LLC

Reason
Failed Impurities/Degradation Specifications: Out of specification for organic impurities
Published
March 27, 2024
Distribution
Nationwide

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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 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

View recall →

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

View recall →

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

View recall →

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

View recall →

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

View recall →

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

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.