Skip to main content
Get Alerts

Data Explorer

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 November 2026.

37,449
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,872
Class I recallsReasonable probability of serious health consequences
24,509
Class II recallsTemporary or medically reversible health consequences
2,932
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 2,096 recalls
Newest recallhttps://www.fsis.usda.gov/recalls-alerts/fsis-issues-public-health-alert-meat-and-poultry-products-due-misbranding-andPublished November 6, 2026
Most affected stateHawaii 200 recalls mention this state

Advertisement

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.

Filters
Recall details
Location
Date range
Sort results
Clear filters
Metric
View
Recalls announced by month (Year to date)

A chart of recalls grouped by month.

Download CSV

Source: FDA and USDA public dataLast updated

Summary (Year to date)

  • 1,956 recalls have been announced year to date.
  • Oct 2026 was 4% higher than the previous complete period (Sep 2026: 209).
  • The highest complete period was Jun 2026 (300).
  • Nov 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 II24,509
Class I9,872
Class III2,932
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,509
Class I9,872
Class III2,932
Not Yet Classified2

Showing 12,641–12,660 of 21,307 recalls

FDA Recall United States TerminatedTerminated: October 9, 2018Historical recordClass II

MUNK PACK INC

Product
Munk Pack PROTEIN COOKIE PEANUT BUTTER CHOCLATE CHIP NET WT…
Reason
Mold growth on product.
Published
May 16, 2018
Distribution
CA,CO,CT,FL,GA,IA,IL,IN,MA,MD,MS,NH,NJ,N…

View recall →

FDA Recall United States TerminatedTerminated: October 9, 2018Historical recordClass II

MUNK PACK INC

Product
Munk Pack PROTEIN COOKIE DOUBLE DARK CHOCOLATE NET WT 2.96oz…
Reason
Mold growth on product.
Published
May 16, 2018
Distribution
CA,CO,CT,FL,GA,IA,IL,IN,MA,MD,MS,NH,NJ,N…

View recall →

FDA Recall United States TerminatedTerminated: May 10, 2018Historical recordClass II

NatureBox, Inc.

Product
Whole Wheat Chocolate Animal Cookies; 5 oz. pouch, 5 lb. Co…
Reason
While packing from a bulk bin of whole wheat chocolate animal cookies, 2 whole wheat vanilla animal cookies were discovered. The vanilla cookies contain soy lecithin that is not declared on the chocolate cookie label.
Published
May 16, 2018
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: October 19, 2018Historical recordClass I

Labrada Nutrition, Inc

Product
Lean Pro 8 Cookies & Cream 1,000g (2.2lb) Tub
Reason
Undeclared egg
Published
May 16, 2018
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: October 19, 2018Historical recordClass I

Labrada Nutrition, Inc

Product
Lean Pro 8 Chocolate 2,268g (5lb) Tub and Lean Pro 8 Chocola…
Reason
Undeclared egg
Published
May 16, 2018
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: October 19, 2018Historical recordClass I

Labrada Nutrition, Inc

Product
Lean Pro 8 Vanilla 2,268g (5lb) Tub
Reason
Undeclared egg
Published
May 16, 2018
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: January 20, 2021Historical recordClass II

Docetaxel injection concentrate, 20 mg/mL, 1 mL vial, Rx only, Winthrop U.S. a business of Sanofi-Aventis U.S. LLC., NDC 0955-1020-01

by Sanofi-Aventis U.S. LLC

Reason
Superpotent drug: over-concentrated vials of Docetaxel injection concentrate 20 mg/mL may have been distributed.
Published
May 9, 2018
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: May 19, 2020Historical recordClass III

Aptensio XR (methylphenidate HCl extended-release) capsules 15 mg Rx Only 90-count bottle. Marketed by: Rhodes Pharmaceuticals L.P., Coventry, RI 02816. Manufactured by: Patheon Manufacturing Services LLC, Greenville, NC 27834. NDC 42858-402-45

by Rhodes Pharmaceuticals, L.P.

Reason
Failed Dissolution Specification: Low dissolution outside of specifications
Published
May 9, 2018
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: February 18, 2022Historical recordClass II

Levofloxacin in 5% Dextrose Injection, 750 mg Levofloxacin (5 mg/mL) in 150 mL of 5% Dextrose, For Intravenous Infusion, Rx only, Manufactured By: Aurobindo Pharma Limited IDA Pashamylaram - 502307, India, Manufactured for AuroMedics Pharma, LLC, NDC 55150-245-52

by AuroMedics Pharma LLC

Reason
Lack of Assurance of Sterility; confirmed customer report of a leaking bags and mold found between the outer bag and the overwrap
Published
May 9, 2018
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: February 18, 2022Historical recordClass II

Levofloxacin in 5% Dextrose Injection, 500 mg Levofloxacin (5 mg/mL) in 100 mL of 5% Dextrose, For Intravenous Infusion, Rx only, Manufactured By: Aurobindo Pharma Limited IDA Pashamylaram - 502307, India, Manufactured for AuroMedics Pharma, LLC, NDC 55150-244-47

by AuroMedics Pharma LLC

Reason
Lack of Assurance of Sterility; confirmed customer report of a leaking bags and mold found between the outer bag and the overwrap
Published
May 9, 2018
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: February 18, 2022Historical recordClass II

Levetiracetam in 0.54% Sodium Chloride Injection, 1,500 mg per 100 mL (15 mg/mL), For Intravenous Infusion Only, Distributed By: AuroMedics Pharma LLC, E. Windsor, NJ 08520, NDC 55150-248-47.

by AuroMedics Pharma LLC

Reason
Lack of Assurance of Sterility; confirmed customer report of a leaking bags and mold found between the outer bag and the overwrap
Published
May 9, 2018
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: February 18, 2022Historical recordClass II

Levetiracetam in 0.75% Sodium Chloride Injection, 1000 mg per 100 mL (10 mg/mL), For Intravenous Infusion Only, Distributed By: AuroMedics Pharma LLC, E. Windsor, NJ 08520, NDC 55150-247-47.

by AuroMedics Pharma LLC

Reason
Lack of Assurance of Sterility; confirmed customer report of a leaking bags and mold found between the outer bag and the overwrap
Published
May 9, 2018
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: February 18, 2022Historical recordClass II

Levetiracetam in 0.82% Sodium Chloride Injection, 500 mg per 100 mL (5 mg/mL), For Intravenous Infusion Only, Distributed By: AuroMedics Pharma LLC, E. Windsor, NJ 08520, NDC 55150-246-47.

by AuroMedics Pharma LLC

Reason
Lack of Assurance of Sterility; confirmed customer report of a leaking bags and mold found between the outer bag and the overwrap
Published
May 9, 2018
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: February 18, 2022Historical recordClass II

Levofloxacin in 5% Dextrose Injection, 250 mg Levofloxacin (5 mg/mL) in 50 mL of 5% Dextrose, For Intravenous Infusion, Rx only, Manufactured By: Aurobindo Pharma Limited IDA Pashamylaram - 502307, India, Manufactured for: AuroMedics Pharma, LLC, NDC 55150-243-46.

by AuroMedics Pharma LLC

Reason
Lack of Assurance of Sterility; confirmed customer report of a leaking bags and mold found between the outer bag and the overwrap
Published
May 9, 2018
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: February 18, 2022Historical recordClass II

Linezolid Injection 600 mg per 300 mL (2 mg/mL) For Intravenous Administration, Rx only, Manufactured By: Aurobindo Pharma Limited IDA Pashamylaram - 502307, India, Manufactured for AuroMedics Pharma, LLC, NDC 55150-242-51

by AuroMedics Pharma LLC

Reason
Lack of Assurance of Sterility; confirmed customer report of a leaking bags and mold found between the outer bag and the overwrap
Published
May 9, 2018
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: November 16, 2018Historical recordClass I

Viable Solutions, LLC

Product
Mitragyna Speciosa Leaf Powder Red Vein Sumatra and Mitragyn…
Reason
Mitragyna Speciosa Leaf Powder Red Vein Sumatra and Mitragyna Speciosa Leaf Powder Red Vein Bali Kratom products are being recalled because they have the potential to be contaminated with Salmonella
Published
May 9, 2018
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: November 16, 2018Historical recordClass I

Viable Solutions, LLC

Product
Mitragyna Speciosa Leaf Powder-Thai Maeng Da, sold under the…
Reason
Mitragyna Speciosa Leaf Powder Thai Maeng Da Kratom product is being recalled because they have the potential to be contaminated with Salmonella
Published
May 9, 2018
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: November 16, 2018Historical recordClass I

Viable Solutions, LLC

Product
Mitragyna Speciosa Leaf Powder-GREEN Horn, sold under the br…
Reason
Mitragyna Speciosa Leaf Powder Green Horn Kratom product is being recalled because they have the potential to be contaminated with Salmonella
Published
May 9, 2018
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: August 17, 2018Historical recordClass II

purely elizabeth.

Product
Chocolate Sea Salt Probiotic Granola, Purely Elizabeth, 8oz,…
Reason
Chocolate Sea Salt Probiotic Granola due to undeclared soy lecithin.
Published
May 9, 2018
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: November 24, 2020Historical recordClass II

PYRIDOXINE Injectable-30 mL MDV Coastal Meds LLC 1759 Medical Park Dr., Ste C Bioloxi, MS 39532

by Coastal Meds, LLC.

Reason
Presence of Particulate matter. Recall due to presence of unknown particulate matter.
Published
May 2, 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.

Reconnecting to the server…

We lost the connection to the server.

Your session has expired.