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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.

37,118
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/gf-blends-recalls-truly-aip-all-purpose-flour-and-bread-mix-and-eat-gangster-flat-bread-pizza-mixPublished September 18, 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 9,761–9,780 of 17,327 recalls

FDA Recall Terminated Historical recordClass I

Hydromorphone, Hydrochloride, Injection, USP CII, 10 mg/mL, Rx Only, 1 mL Single-dose Vial, High Potency Formulation. Mfd For: Teva Parenteral Medicines, Inc., Irvine, CA 92618. NDC: 0703-0110-01

by Pfizer Inc.

Reason
Non-Sterility: Confirmed customer complaints of glass product container vials that may be empty or cracked.
Published
March 21, 2018
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Sermorelin Acetate, powder, a) 1 GM-bottle (NDC58597-8092-1) b) 5 GM-bottle (NDC 58597-8092-2) c) 10 GM-bottle (NDC 58597-8092-4) API American Pharmaceutical Ingredients

by American Pharmaceutical Ingredients LLC

Reason
Stability Data Does Not Support Expiry: Stability data from manufacturer does not support expiration dates listed.
Published
March 21, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Oxytocin USP, powder, 1g-bottle, API American Pharmaceutical Ingredients, NDC 58597-7042-3

by American Pharmaceutical Ingredients LLC

Reason
Stability Data Does Not Support Expiry: Stability data from manufacturer does not support expiration dates listed.
Published
March 21, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Psoriasin Daytime Relief Cream with Vitamin D & Oatmeal, (Coal Tar 1.25%), packagedin 57 g plastic tubes, Distributed by: ALVA-AMCO Pharmacal Cos., Inc., Niles, IL 60714, USA. NDC 52389-745-56, UPC 0 72959 01045 4.

by Alva-Amco Pharmacal Companies., Inc.

Reason
Subpotent Drug: The product has failed to maintain its label claim of coal tar throughout its labeled 24-month expiry period.
Published
March 21, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

methylPREDNISolone Sodium Succinate for Injection, USP, 1 gram* per vial, Single-Dose Vial, Rx only, Mfd. for: Sagent Pharmaceuticals, Schaumburg, IL 60195 (USA), Made in India. NDC 25021-810-30.

by Sagent Pharmaceuticals Inc

Reason
Failed Impurities/Degradation Specifications: High out of specification results for an impurity.
Published
March 21, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

methylPREDNISolone Sodium Succinate for Injection, USP, 125 mg* per vial, Single-Dose Vial, Rx only, Mfd. for: Sagent Pharmaceuticals, Schaumburg, IL 60195 (USA), Made in India. NDC 25021-808-10.

by Sagent Pharmaceuticals Inc

Reason
Failed Impurities/Degradation Specifications: High out of specification results for an impurity.
Published
March 21, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

methylPREDNISolone Sodium Succinate for Injection, USP, 40 mg* per vial, Single-Dose Vial, Rx only, Mfd. for: Sagent Pharmaceuticals, Schaumburg, IL 60195 (USA), Made in India. NDC 25021-807-05.

by Sagent Pharmaceuticals Inc

Reason
Failed Impurities/Degradation Specifications: High out of specification results for an impurity.
Published
March 21, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Plant Devas Inc

Product
Ayurvedic Face Care Kit; Each kit contains: Coconut Cream…
Reason
FDA Office of Colors and Cosmetics sampled product and found virulent and excessive numbers of microorganisms.
Published
March 21, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Plant Devas Inc

Product
Blemish Face Care Kit; Each kit contains: Tea Tree Gel Cle…
Reason
FDA Office of Colors and Cosmetics sampled product and found virulent and excessive numbers of microorganisms.
Published
March 21, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Plant Devas Inc

Product
Blue Face Care Kit; Each kit contains: Blue Lavender Clean…
Reason
FDA Office of Colors and Cosmetics sampled product and found virulent and excessive numbers of microorganisms.
Published
March 21, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Plant Devas Inc

Product
Rose Face Care Kit; Each kit contains: Rose Cleansing Milk…
Reason
FDA Office of Colors and Cosmetics sampled product and found virulent and excessive numbers of microorganisms.
Published
March 21, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Plant Devas Inc

Product
Green Tea Clay; 2.1 and 0.17 oz. jars evanhealy Han…
Reason
FDA Office of Colors and Cosmetics sampled product and found virulent and excessive numbers of microorganisms.
Published
March 21, 2018
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Plant Devas Inc

Product
French Rose Clay; with Mineral Rish Moroccan Rhassoul Clay…
Reason
FDA Office of Colors and Cosmetics sampled product and found virulent and excessive numbers of microorganisms.
Published
March 21, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Plant Devas Inc

Product
Lemongrass Facial Polish with Oats, Fengreek & Neem. 3 oz c…
Reason
FDA Office of Colors and Cosmetics sampled product and found virulent and excessive numbers of microorganisms.
Published
March 21, 2018
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Plant Devas Inc

Product
Clay Mask Kit; 2 glass jars of clay: Green Tea Clay 0.3 oz.…
Reason
FDA Office of Colors and Cosmetics sampled product and found virulent and excessive numbers of microorganisms.
Published
March 21, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Kodiak Cakes, LLC

Product
Kodiak Cakes, Energy Waffles, Blueberry Chia, Net Wt 10.72 O…
Reason
The frozen waffle product contains whey but fails to declare the major food allergen "milk" on the label
Published
March 21, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Progressive Laboratories, Inc

Product
Xenesta Nuvive Womens 90 count packaged in a white plastic b…
Reason
Recalled dietary supplements may contain undeclared milk.
Published
March 21, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Progressive Laboratories, Inc

Product
Xenesta Nuvive Mens 90 count packaged in an white plastic bo…
Reason
Recalled dietary supplements may contain undeclared milk.
Published
March 21, 2018
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

Progressive Laboratories, Inc

Product
Thyroid Resilience 120 count bottle packaged in an amber pla…
Reason
Recalled dietary supplements may contain undeclared milk.
Published
March 21, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Progressive Laboratories, Inc

Product
Testosterzone 180 count bottle packaged in an amber plastic…
Reason
Recalled dietary supplements may contain undeclared milk.
Published
March 21, 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.