Skip to main content

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 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
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.

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)

  • 1,739 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 341–360 of 37,271 recalls

FDA Recall Ongoing2026 recordClass II

SEMAGLUTIDE 10mg (5mg/mL), Glycine 10 mg (5mg/mL), 2 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-722-02

by Apollo Care, LLC

Reason
Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
Published
August 19, 2026
Distribution
Nationwide

View recall →

FDA Recall Ongoing2026 recordClass II

SEMAGLUTIDE 7.5mg (5mg/mL), Glycine 7.5 mg (5mg/mL), 1.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-721-01

by Apollo Care, LLC

Reason
Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
Published
August 19, 2026
Distribution
Nationwide

View recall →

FDA Recall Ongoing2026 recordClass II

SEMAGLUTIDE 5mg (1mg/mL), Glycine 25 mg (5mg/mL), 5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202.NDC 71170-712-03

by Apollo Care, LLC

Reason
Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
Published
August 19, 2026
Distribution
Nationwide

View recall →

FDA Recall Ongoing2026 recordClass II

SEMAGLUTIDE 2.5mg (1mg/mL), Glycine 12.5 mg (5mg/mL), 2.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-711-02

by Apollo Care, LLC

Reason
Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
Published
August 19, 2026
Distribution
Nationwide

View recall →

FDA Recall Ongoing2026 recordClass II

SEMAGLUTIDE 0.9mg (0.9 mg/mL), 1 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-810-01

by Apollo Care, LLC

Reason
Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
Published
August 19, 2026
Distribution
Nationwide

View recall →

FDA Recall Ongoing2026 recordClass II

SEMAGLUTIDE 9mg (4.5 mg/mL), 2 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-822-02

by Apollo Care, LLC

Reason
Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
Published
August 19, 2026
Distribution
Nationwide

View recall →

FDA Recall Ongoing2026 recordClass II

SEMAGLUTIDE 4.5mg (0.9 mg/mL), 5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-812-03

by Apollo Care, LLC

Reason
Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
Published
August 19, 2026
Distribution
Nationwide

View recall →

FDA Recall Ongoing2026 recordClass II

SEMAGLUTIDE 6.75mg (4.5 mg/mL), 1.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202 NDC 71170-821-01

by Apollo Care, LLC

Reason
Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
Published
August 19, 2026
Distribution
Nationwide

View recall →

FDA Recall Ongoing2026 recordClass II

SEMAGLUTIDE 2.25MG (0.9 mg/mL), 2.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202 NDC 71170-811-02

by Apollo Care, LLC

Reason
Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
Published
August 19, 2026
Distribution
Nationwide

View recall →

FDA Recall Ongoing2026 recordClass II

SEMAGLUTIDE 12.5MG (2.5MG/mL), 5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-495-05

by Apollo Care, LLC

Reason
Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
Published
August 19, 2026
Distribution
Nationwide

View recall →

FDA Recall Ongoing2026 recordClass II

Diovan (valsartan) 160 mg, 90 tablets, Rx only, Manufactured by: Patheon Manufacturing Services LLC, Greenville, NC 27834, Distributed by: Novartis Pharmaceutical Corp, East Hanover, NJ 07936, NDC 0078-0359-34

by Novartis Pharmaceuticals Corporation

Reason
Failed Dissolution Specifications
Published
August 19, 2026
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: September 18, 20262026 recordClass I

MIDWEST POULTRY SERVC C/O H & LELECTRIC

Product
Grade A White In-shell Chicken eggs packaged in the followin…
Reason
Possible Salmonella Enteritidis
Published
August 19, 2026
Distribution
Arkansas, Louisiana, Mississippi, New Me…

View recall →

FDA Recall United States TerminatedTerminated: September 18, 20262026 recordClass I

MIDWEST POULTRY SERVC C/O H & LELECTRIC

Product
Grade A Brown In-shell Chicken eggs packaged in the followin…
Reason
Possible Salmonella Enteritidis
Published
August 19, 2026
Distribution
Arkansas, Louisiana, Mississippi, New Me…

View recall →

FDA Recall United States Ongoing2026 recordClass I

Bazzini LLC

Product
Dark Chocolate Coconut Almond Bites, 3.17oz, Plastic Pouches…
Reason
Undeclared peanuts
Published
August 19, 2026
Distribution
The product was distributed to WA.

View recall →

FDA Recall United States Ongoing2026 recordClass III

FlavorsandColor.Com

Product
Honeyville YELLOW COLOR 1 GALLON NFI: WATER, FD&C YELLOW #5…
Reason
Undeclared Red #40.
Published
August 19, 2026
Distribution
Product is sold to independent manufactu…

View recall →

FDA Recall United States TerminatedTerminated: August 27, 20262026 recordClass II

SHEANDRO LLC

Product
Vodka Tomato Sauce, NET WT. 24 oz / 680g, glass jar packed 1…
Reason
Label declares cream and cheese, but Milk is not declared
Published
August 19, 2026
Distribution
Product distributed in Florida

View recall →

FDA Recall United States Status not reported2026 record

Prince Bakery Inc Issues Allergy Alert on Undeclared Milk and Sesame in Prince Bakery Breads

Reason
Prince Bakery of Bronx, New York is recalling Prince brand Sesame Italian Bread, Large Italian Bread, Large Sesame French Bread, Long Sesame French Bread and Pan de Manteca Spanish Style Bread because they may contain undeclared sesame or milk. People who have an allergy or severe sensitivity to s
Published
August 19, 2026

View recall →

FDA Recall United States Status not reported2026 record

Updated – Dreyer’s Grand Ice Cream, Inc. Issues Voluntary Recall on Select Outshine Fruit Bars Due to Possible Foreign Matter Contamination

Reason
August 18, 2026 - Dreyer’s Grand Ice Cream, Inc. is voluntarily recalling a limited number of select flavors of Outshine Fruit Bars due to possible foreign material contamination with glass. Products affected include Outshine Strawberry, Watermelon, Grape, Tangerine and Black Cherry 6-Count 2.5 ounc
Published
August 18, 2026

View recall →

FDA Recall United States Status not reported2026 record

L-Nutra Issues Allergy Alert on Undeclared Tree Nuts in Prolon Brand Apulian Almond & Cocoa Spread

Reason
L-Nutra of Culver City, California is recalling Prolon brand Apulian Almond & Cocoa Spread because it contains undeclared cashew, pistachio, and hazelnut. People who have an allergy or severe sensitivity to cashew, pistachio, and/or hazelnut run the risk of serious or life-threatening allergic react
Published
August 18, 2026

View recall →

USDA FSIS Recall United States Status not reported2026 record

Indus Foods, LLC DBA Gangothri Foods Recalls Ready-To-Eat Pickled Goat and Chicken Products Produced Without Benefit of Inspection

Reason
<img align="left" hspace="5" src="https://www.fsis.usda.gov/sites/default/files/2023-04/Icon-Recalls.png"/> WASHINGTON, Aug. 17, 2026 - Indus Foods, LLC, doing business as Gangothri Foods, an Austin, Tex. firm, is recalling approximately 1,626 pounds of ready-to-eat (RTE) pickled goat and chicken products...
Published
August 17, 2026

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.