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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.

37,066
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/whole-foods-market-issues-allergy-alert-undeclared-egg-cabricharme-cheesePublished September 11, 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 3,881–3,900 of 17,333 recalls

FDA Recall Terminated Historical recordClass II

MILK OF MAGNESIA USP, 2400 mg/10 mL, Magnesium Hydroxide, 30 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr., Suite 233, Livonia, MI 48152, NDC 0904-6840-72.

by Plastikon Healthcare LLC

Reason
CGMP Deviations: products manufactured under conditions which reflect manufacturing processes that were not adequately controlled.
Published
September 14, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

MILK OF MAGNESIA USP, 2400 mg/30 mL, Magnesium Hydroxide, 30 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr., Suite 233, Livonia, MI 48152, NDC 0904-6846-73.

by Plastikon Healthcare LLC

Reason
CGMP Deviations: products manufactured under conditions which reflect manufacturing processes that were not adequately controlled.
Published
September 14, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass I

Magnesium Hydroxide 2400 mg, Aluminum Hydroxide 2400 mg, Simethicone 240 mg MAX, per 30 mL Oral Suspension, 30 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr., Suite 233, Livonia, MI 48152, NDC 0904-6839-73

by Plastikon Healthcare LLC

Reason
Microbial Contamination of Non-Sterile Products.
Published
September 14, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass I

Magnesium Hydroxide 1200 mg, Aluminum Hydroxide 1200 mg, Simethicone 120 mg per 30 mL, 30 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr., Suite 233, Livonia, MI 48152, NDC 0904-6838-73

by Plastikon Healthcare LLC

Reason
Microbial Contamination of Non-Sterile Products.
Published
September 14, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass I

MILK OF MAGNESIA USP, 2400 mg/10 mL, Magnesium Hydroxide, 30 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr., Suite 233, Livonia, MI 48152, NDC 0904-6840-72.

by Plastikon Healthcare LLC

Reason
Microbial Contamination of Non-Sterile Products.
Published
September 14, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass I

MILK OF MAGNESIA USP, 2400 mg/30 mL, Magnesium Hydroxide, 30 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr., Suite 233, Livonia, MI 48152, NDC 0904-6846-73.

by Plastikon Healthcare LLC

Reason
Microbial Contamination of Non-Sterile Products
Published
September 14, 2022
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

King's Hawaiian Bakery

Product
King's Hawaiian 10.5 oz. Pretzel Hamburger Buns (UPC 7343500…
Reason
Ingredient used to manufacture pretzel products may have been contaminated with Cronobacter sakazakii, and/or Clostridium botulinum.
Published
September 14, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Triamcinolone Acetonide Cream USP, 0.1%, 80 g tube, Rx Only, Manufactured By Perrigo, Bronx, NY 10457, Distributed By Perrigo, Allegan, MI 49010, NDC 45802-064-36.

by Padagis US LLC

Reason
CGMP Deviations: Product complaints reporting the product to have a gritty texture and lack of effectiveness.
Published
September 7, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Neomycin Sulfate Tablets, USP 500 mg , 100-count bottles, Rx only, Distributed by: TEVA PHARMACEUTICALS USA, INC North Wales, PA 19454, NDC 0093-1177-01

by Teva Pharmaceuticals USA Inc

Reason
CGMP Deviations: A foreign matter identified as teflon was found in the Active Pharmaceutical Ingredient (API) used in the manufacture of Neomycin Sulfate Tablets, USP 500 mg.
Published
September 7, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Nighttime Sleep-Aid (doxylamine succinate HCl) tablets, 25 mg, 48-count blisters per carton, Distributed by: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895, UPC 0 50428 34873 4.

by LNK International, Inc.

Reason
Labeling: Not Elsewhere Classified: Carton incorrectly identifies product as doxylamine succinate HCl, however the product is doxylamine succinate.
Published
September 7, 2022
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass III

Timolol Maleate Ophthalmic Solution, USP, 0.5%, 5 x 0.3 mL Single-Dose Vials, Rx Only, Sterile, Manufactured for: Akorn, Inc., Lake Forest, IL 60045. NDC 17478-189-24

by Akorn, Inc

Reason
Failed Impurities/Degradation Specifications: Identification of an unknown impurity at the 12-month stability point.
Published
September 7, 2022
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Colgate Whitening Mouthwash, OPTIC WHITE ICY FRESH MINT. 16 fl. OZ. (1 pt) 473 mL UPC 0 35000 67111 0. Dist. by: Colgate-Palmolive Co. New York, NY 10022 U.S.A.

by Family Dollar Stores, Llc.

Reason
cGMP deviation: Product held outside of appropriate temperature storage conditions.
Published
September 7, 2022
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Colgate Anticavity Fluoride Toothpaste OPTIC WHITE STAIN FIGHTER CLEAN MINT PASTE. Net Wt. 4.2 OZ. (119 g) UPC 0 35000 45836 0. Dist. by: Colgate-Palmolive Company New York, NY 10022 U.S.A.

by Family Dollar Stores, Llc.

Reason
cGMP deviation: Product held outside of appropriate temperature storage conditions.
Published
September 7, 2022
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Colgate Anticavity Fluoride Toothpaste, OPTIC WHITE with CHARCOAL COOL MINT PASTE, Net Wt. 4.2 OZ. UPC 0 35000 97872 1. Dist. by: Colgate-Palmolive Company New York, NY 10022 U.S.A.

by Family Dollar Stores, Llc.

Reason
cGMP deviation: Product held outside of appropriate temperature storage conditions.
Published
September 7, 2022
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Colgate Anticavity Fluoride Toothpaste, OPTIC WHITE ADVANCED ICY FRESH, Net Wt. 3.2 OZ. (90 g) UPC 0 35000 97159 3. Dist. by: Colgate-Palmolive Company New York, NY 10022 U.S.A.

by Family Dollar Stores, Llc.

Reason
cGMP deviation: Product held outside of appropriate temperature storage conditions.
Published
September 7, 2022
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Colgate Anticavity Fluoride Toothpaste, OPTIC WHITTE RENEWAL, 3% Hydrogen Peroxide, High Impact White, Net Wt. 3.0 OZ. (85 g) UPC 0 35000 97008 4. Dist. by: Colgate-Palmolive Company New York, NY 10022 U.S.A.

by Family Dollar Stores, Llc.

Reason
cGMP deviation: Product held outside of appropriate temperature storage conditions.
Published
September 7, 2022
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Colgate Anticavity Fluoride Toothpaste, OPTIC WHITE PRO SERIES, Stain Prevention, 5% Hydrogen Peroxide, Net Wt. 2.1 OZ. (59 g) UPC 0 35000 99658 9. Dist. by: Colgate-Palmolive Company New York, NY 10022 U.S.A.

by Family Dollar Stores, Llc.

Reason
cGMP deviation: Product held outside of appropriate temperature storage conditions.
Published
September 7, 2022
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Clinical Innovations, LLC

Product
Sweetums 24% sucrose solution with preservative. Vials conta…
Reason
Firm received complaints of leaking, black liquid, and black particulates in the product vials.
Published
September 7, 2022
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Clinical Innovations, LLC

Product
Sweetums 24% sucrose solution preservative free. Vials conta…
Reason
Firm received complaints of leaking, black liquid, and black particulates in the product vials.
Published
September 7, 2022
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Clinical Innovations, LLC

Product
Sweetums 24% Sucrose Solution Preservative Free 15 mL cups V…
Reason
Firm received complaints of leaking cups, black liquid, and black particulates in the 24% Sucrose Solution.
Published
September 7, 2022
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.