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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 October 2026.

37,271
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,852
Class I recallsReasonable probability of serious health consequences
24,397
Class II recallsTemporary or medically reversible health consequences
2,897
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 2,085 recalls
Newest recallhttps://www.fsis.usda.gov/recalls-alerts/kayem-foods-inc--recalls-meat-and-poultry-products-due-possible-temperature-abusePublished October 17, 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)

  • 1,739 recalls have been announced year to date.
  • Sep 2026 was 15% higher than the previous complete period (Aug 2026: 182).
  • The highest complete period was Jun 2026 (300).
  • Oct 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 II24,397
Class I9,852
Class III2,897
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,397
Class I9,852
Class III2,897
Not Yet Classified2

Showing 3,461–3,480 of 17,287 recalls

FDA Recall TerminatedTerminated: May 12, 2024Historical recordClass II

Verapamil Hydrochloride Extended-Release Tablets, USP, 120 mg, Rx Only, 100 Tablets per Carton (10 x 10), Distributed by: American Health Packaging, Columbus, Ohio 43217. NDC Carton: 60687-493-01; NDC Unit Dose: 60687-493-11.

by Amerisource Health Services LLC

Reason
Failed Dissolution Specification: Out of specification dissolution results at time point zero. The OOS was above specified values.
Published
March 15, 2023
Distribution
Nationwide

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FDA Recall TerminatedTerminated: May 19, 2026Historical recordClass II

Heparin Sodium Injection, USP, 20,000 USP units per mL, 25 x 1 mL Multi-Dose Vials, Rx Only, For Intravenous or Subcutaneous Use, Mfd. for: Sagent Pharmaceuticals, Schaumburg, IL 60195; Made in India, NDC carton: 25021-404-01

by Sagent Pharmaceuticals Inc

Reason
Labeling: Not elsewhere classified
Published
March 15, 2023
Distribution
Nationwide

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FDA Recall TerminatedTerminated: March 13, 2024Historical recordClass II

Heparin Sodium, 25,000USP units per 250 mL, (100 USP units per mL) in 5% Dextrose Injection, 250 mL Excel Container, B.Braun Medical Inc, Bethlehem, PA. 18018-3524 USA. NDC 0264-9587-20.

by B. Braun Medical Inc

Reason
Subpotent Drug: low Anti-Factor IIa potency.
Published
March 15, 2023
Distribution
Nationwide

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FDA Recall CompletedHistorical recordClass II

Brimonidine Tartrate Ophthalmic Solution 0.15%, Rx Only, Packaged as: a) 5 mL dropper bottle, NDC 60505-0564-1, UPC 3 60505 05641 5; b) 10 mL dropper bottle NDC 60505-0564-2, UPC 3 60505 05642 2; c) 15 mL dropper bottle, NDC 60505-0564-3, UPC 3 60505 05643 9; Manufactured by: Apotex Inc. Toronto, Ontario Canada M9L 1T9 Manufactured for: Apotex Corp. Weston, FL 33326

by Apotex Corp.

Reason
Lack of sterility assurance: Cracks have developed in some of the units caps of Brimonidine tartrate ophthalmic solution bottles. There is a possibility the broken cap may impact sterility.
Published
March 15, 2023
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: April 3, 2025Historical recordClass II

DAILY HARVEST

Product
Daily Harvest French Lentil + leek Crumbles, Item ID L02-VEG…
Reason
Product is linked to complaints of gastrointestinal illness.
Published
March 15, 2023
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: April 14, 2023Historical recordClass I

Chukar Cherry Company Inc.

Product
Chukar Cherries Cherry Bombs Bits 'n Pieces, item #21508, ne…
Reason
undeclared hazelnuts
Published
March 15, 2023
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: May 3, 2023Historical recordClass II

Wismettac Asian Foods, Inc.

Product
SPICE SHICHIMI TOGARASHI 300g UPC: 074410341213 Brand: Shir…
Reason
Product was found to contain sesame that were not declared on the ingredient label. Potential for product mix up, so product i being recalled out of an abundance of caution
Published
March 15, 2023
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: May 3, 2023Historical recordClass II

Wismettac Asian Foods, Inc.

Product
Chili Pepper Powder (ICHIMI TOGARASHI) 300g UPC: 07441034116…
Reason
Product was found to contain sesame that were not declared on the ingredient label.
Published
March 15, 2023
Distribution
Nationwide

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FDA Recall TerminatedTerminated: April 30, 2024Historical recordClass II

Carbidopa and Levodopa Tablets, USP 25 mg/100 mg, 10x10 Unit Dose carton, Rx Only, Manufactured in Czech Republic by: Teva Czech Industries, s.r.o. Opava-Komarov, Czech Republic, Manufactured for: Teva Pharmaceuticals USA, Inc. Parsippany, NJ 07054, Packaged and Distributed by: Major Pharmaceuticals Indianapolis, IN 46268 USA. NDC 0904-7257-61, UPC 3 09047 25761 4

by The Harvard Drug Group

Reason
Packaging defect: observed packaging defect, blister packaging inadequately sealed.
Published
March 8, 2023
Distribution
Nationwide

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FDA Recall TerminatedTerminated: June 21, 2023Historical recordClass III

Fentanyl 1,500 mcg/30 mL syringe, Injection for Intravenous Use, Concentration = 50 mcg/mL, Preservative Free, Rx Only, Single Dose Container, SCA Pharmaceuticals, Windsor CT 06095, NDC# 70004-0200-16.

by SCA Pharmaceuticals

Reason
Subpotent Drug
Published
March 8, 2023
Distribution
Nationwide

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FDA Recall TerminatedTerminated: September 24, 2024Historical recordClass II

Phenylephrine HCl in 0.9% Sodium Chloride Injection, USP, 50 mg/250 mL (200 mcg/mL), 250 mL Single-Dose Container bottle, packaged in 15 x 1 IV Bottles per carton, Rx Only, Nephron 503B Outsourcing Facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC 69374-321-25.

by Nephron Sterile Compounding Center LLC

Reason
Lack of Assurance of Sterility
Published
March 8, 2023
Distribution
Nationwide

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FDA Recall TerminatedTerminated: September 24, 2024Historical recordClass II

Phenylephrine HCl Injection, USP, 0.8 mg/10 mL (80 mcg/mL), 10 mL Single-Dose Vial, packaged in 30 x 10 mL Single-Dose Vials per carton, 12 x 30 Vials Carton per case, Rx Only, Nephron 503B Outsourcing Facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC 69374-301-10.

by Nephron Sterile Compounding Center LLC

Reason
Lack of Assurance of Sterility
Published
March 8, 2023
Distribution
Nationwide

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FDA Recall TerminatedTerminated: September 24, 2024Historical recordClass II

Phenylephrine HCl Injection, USP, 0.4 mg/10 mL (40 mcg/mL), 10 mL Single-Dose Vial, packaged in 30 x 10 mL Single-Dose Vials per carton, 12 x 30 Vials Carton per case, Rx Only, Nephron 503B Outsourcing Facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC 69374-305-10.

by Nephron Sterile Compounding Center LLC

Reason
Lack of Assurance of Sterility
Published
March 8, 2023
Distribution
Nationwide

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FDA Recall TerminatedTerminated: September 24, 2024Historical recordClass II

Phenylephrine HCl Injection, USP, 1 mg/10 mL (100 mcg/mL), 10 mL Single-Dose Vial, packaged in 30 x 10 mL Sterile Single-Dose Vials per carton, 12 x 30 Vials Carton per case, Rx Only, Nephron 503B Outsourcing Facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC 69374-302-10.

by Nephron Sterile Compounding Center LLC

Reason
Lack of Assurance of Sterility
Published
March 8, 2023
Distribution
Nationwide

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FDA Recall TerminatedTerminated: September 24, 2024Historical recordClass II

Norepinephrine Bitartrate in 0.9% Sodium Chloride Injection, USP, 16 mg/250 mL (64 mcg/mL*), 250 mL Single-Dose Container bottle, packaged in 15 IV Bottles per carton, Rx Only, Nephron 503B Outsourcing Facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC 69374-315-25.

by Nephron Sterile Compounding Center LLC

Reason
Lack of Assurance of Sterility
Published
March 8, 2023
Distribution
Nationwide

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FDA Recall TerminatedTerminated: September 24, 2024Historical recordClass II

Norepinephrine Bitartrate in 0.9% Sodium Chloride Injection, USP, 4 mg/250 mL (16 mcg/mL*), 250 mL Single-Dose Container bottle, packaged in 15 IV Bottles per carton, Rx Only, Nephron 503B Outsourcing Facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC 69374-319-25.

by Nephron Sterile Compounding Center LLC

Reason
Lack of Assurance of Sterility
Published
March 8, 2023
Distribution
Nationwide

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FDA Recall TerminatedTerminated: September 24, 2024Historical recordClass II

Norepinephrine Bitartrate in 0.9% Sodium Chloride Injection, USP, 8 mg/250 mL (32 mcg/mL*), 250 mL Single-Dose Container, packaged in 15 x 1 IV Bottles per carton, Rx Only, Nephron 503B Outsourcing Facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC 69374-316-25.

by Nephron Sterile Compounding Center LLC

Reason
Lack of Assurance of Sterility
Published
March 8, 2023
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: September 24, 2024Historical recordClass II

Diltiazem HCl in 0.7% Sodium Chloride Injection, 125 mg/125 mL (1 mg/mL), 125 mL Single-Dose Container bottle, packaged in 15 x 1 IV Bottles per carton, Rx Only, Nephron 503B Outsourcing Facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC 69374-997-15.

by Nephron Sterile Compounding Center LLC

Reason
Lack of Assurance of Sterility
Published
March 8, 2023
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: December 20, 2023Historical recordClass III

Avicel PH-200 NF, Microcrystalline Cellulose, NF, Ph. Eur., Jp, Net Content/Gross Weight 20.0 KG / 21.1 KG bulk container, Manufactured by: DuPont Nutrition USA, Inc., 1301 Ogletown Road, Newark, DE 19711, USA. Headquarters: DuPont Nutrition Biosciences ApS, Langebrogade 1, Copenhagen, Denmark

by DuPont Nutrition USA, Inc

Reason
Failed Impurities/Degradation Specifications: Out of specification results obtained for conductivity.
Published
March 8, 2023
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: December 20, 2023Historical recordClass III

Avicel PH- 102 NF, Microcrystalline Cellulose, NF, Ph. Eur., Jp, Net Content/Gross Weight 20.0 KG / 21.1 KG bulk container, Manufactured by: DuPont Nutrition USA, Inc., 1301 Ogletown Road, Newark, DE 19711, USA. Headquarters: DuPont Nutrition Biosciences ApS, Langebrogade 1, Copenhagen, Denmark

by DuPont Nutrition USA, Inc

Reason
Failed Impurities/Degradation Specifications: Out of specification results obtained for conductivity.
Published
March 8, 2023
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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