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 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.

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)

  • 1,527 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 3,281–3,300 of 19,916 recalls

FDA Recall Terminated Historical recordClass II

CARDIOPLEGIA SOLUTION, 24 mEq K, Maintenance 8:1, Low Potassium, Total volume = 500 mL, EVA Bag, Rx only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Pheonix, AZ 85043, NDC: 72196-0105-1

by Central Admixture Pharmacy Services, Inc.

Reason
Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Published
September 6, 2023
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

CARDIOPLEGIA SOLUTION, HIGH K, Induction 4:1, Plasmalyte/Tromethamine, High Potassium, EVA Bags, total volume = 500 mL, Rx Only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Pheonix, AZ 85043, NDC: 72196-0111-1

by Central Admixture Pharmacy Services, Inc.

Reason
Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Published
September 6, 2023
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

CARDIOPLEGIA SOLUTION, 60 mEq K, Induction 4:1, HIGH POTASSIUM, Total Volume = 830 mL, EVA Bag, RX only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Pheonix, AZ 85043, NDC: 72196-0100-1

by Central Admixture Pharmacy Services, Inc.

Reason
Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Published
September 6, 2023
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

CARDIOPLEGIA SOLUTION, 20 mEq K, Maintenance 4:1, Low Potassium, Total Volume = 810 mL, EVA Bag, Rx only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Phoenix, AZ 85043, NDC: 72196-0103-1

by Central Admixture Pharmacy Services, Inc.

Reason
Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Published
September 6, 2023
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Lyons Magnus LLC

Product
GFS Harvest Valley Grape Juice packaged in 4 fl oz opaque wh…
Reason
Signs of bloating in juice cups
Published
September 6, 2023
Distribution
AR, FL, GA, IA, KY, LA, MI, NC, OH, PA,…

View recall →

FDA Recall United States Terminated Historical recordClass II

Lyons Magnus LLC

Product
GFS Harvest Valley Cranberry/Grape Juice packaged in 4 fl oz…
Reason
Signs of bloating in juice cups
Published
September 6, 2023
Distribution
AR, FL, GA, IA, KY, LA, MI, NC, OH, PA,…

View recall →

FDA Recall United States Terminated Historical recordClass II

Lyons Magnus LLC

Product
Lyons Grape Juice packaged in 4 fl oz opaque white plastic c…
Reason
Signs of bloating in juice cups
Published
September 6, 2023
Distribution
AR, FL, GA, IA, KY, LA, MI, NC, OH, PA,…

View recall →

FDA Recall United States Terminated Historical recordClass II

Moore Family Farms Creamery

Product
Moore Family Farms and Creamery Cheddar Cheese Curds BLT, 1…
Reason
May contain elevated coliform count and generic E. coli.
Published
September 6, 2023
Distribution
IA

View recall →

FDA Recall United States Terminated Historical recordClass II

Moore Family Farms Creamery

Product
Moore Family Farms and Creamery Cheddar Cheese Curds Loaded…
Reason
May contain elevated coliform count and generic E. coli.
Published
September 6, 2023
Distribution
IA

View recall →

FDA Recall United States Terminated Historical recordClass II

Moore Family Farms Creamery

Product
Moore Family Farms and Creamery Cheddar Cheese Curds Cucumbe…
Reason
May contain elevated coliform count and generic E. coli.
Published
September 6, 2023
Distribution
IA

View recall →

FDA Recall United States Terminated Historical recordClass II

Moore Family Farms Creamery

Product
Moore Family Farms and Creamery Cheddar Cheese Curds, 1 lb p…
Reason
May contain elevated coliform count and generic E. coli.
Published
September 6, 2023
Distribution
IA

View recall →

FDA Recall Terminated Historical recordClass II

NAD+ 200mg/ml, 10ml vials, Tailor Made Compounding.

by TMC Acquisitions LLC dba Tailor Made Compounding

Reason
Lack of Assurance of Sterility
Published
August 30, 2023
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Semaglutide/Cyanocobalamin 2mg/0.4mg/mL, 1mLvials, Tailor Made Compounding.

by TMC Acquisitions LLC dba Tailor Made Compounding

Reason
Lack of Assurance of Sterility
Published
August 30, 2023
Distribution
Nationwide

View recall →

FDA Recall Completed Historical recordClass III

Bendamustine HCl Injection, 100mg/4mL (25mg/mL), One 4 mL Multiple-Dose Vial, Rx only, Manufactured for Baxter Healthcare Corporation, Deerfield, IL 60015, NDC 10019-079-01.

by Baxter Healthcare Corporation

Reason
Labeling: Missing Label; customer complaint received that labels were partially or completely peeled off injection vial.
Published
August 30, 2023
Distribution
Nationwide

View recall →

FDA Recall Completed Historical recordClass II

Lugol's (Strong Iodine Solution USP), Each mL contains Iodine 0.05gm and potassium iodide 0.100gm, 8mL Single Use Vials, Rx Only, Manufactured for CooperSurgical, Trumbull, CT 06611, NDC 59365-6064-0, Ref 6064.

by Ecometics, Inc.

Reason
CGMP Deviations: Products not manufactured under current good manufacturing practices.
Published
August 30, 2023
Distribution
Nationwide

View recall →

FDA Recall Completed Historical recordClass II

AstrinGyn (Ferric Subsulfate) Aqueous, 259 mg/g, 8 gm Single Use Vials, Manufactured for CooperSurgical, Trumbull, CT 06611, NDC 59365-6065-0, Ref 6065.

by Ecometics, Inc.

Reason
CGMP Deviations: Products not manufactured under current good manufacturing practices.
Published
August 30, 2023
Distribution
Nationwide

View recall →

FDA Recall Completed Historical recordClass II

activator concentrate, Sodium Fluoride 0.96% in Activator Concentrate; 0.08% in diluted Activator Solution, Net 1 FL. OZ., Manufactured for: All USA Direct, LLC, Broadview, IL 60155.

by Ecometics, Inc.

Reason
CGMP Deviations: Products not manufactured under current good manufacturing practices.
Published
August 30, 2023
Distribution
Nationwide

View recall →

FDA Recall Completed Historical recordClass II

Unguentine Ointment, (Camphor 3.0%, Phenol 2.5%, Tannic Acid 2.2%, Zinc Oxide 6.6%), labeled as a) NET WT 1 OZ (28 g) tubes, Improved Formula, UPC 0 11169 10216 0, and b) NET WT 1 OZ (28.3g) tubes, Maximum Strength, UPC 0 11169 11250 3, Distributed by: Oakhurst Company, Levittown, NY 11756.

by Ecometics, Inc.

Reason
CGMP Deviations: Products not manufactured under current good manufacturing practices.
Published
August 30, 2023
Distribution
Nationwide

View recall →

FDA Recall Completed Historical recordClass II

ALCOLADO RELAMPAGO (Menthol and Camphor), 1% and 1.5% respectively, packaged in a 7 FLUID OZ (207 ml) bottles, UPC 7 18864 20102 9 and b) 16 FLUID OZ (472 ml) bottles, UPC 7 18864, 20110 4, Distributed by: The Larkspur Group, Inc., Norwalk, CT 06854.

by Ecometics, Inc.

Reason
CGMP Deviations: Products not manufactured under current good manufacturing practices.
Published
August 30, 2023
Distribution
Nationwide

View recall →

FDA Recall Completed Historical recordClass II

YAGER'S LINIMENT (Camphor and Turpentine Oil) 3.1% and 8.12% respectively, packaged in a) 4 FL OZ (118 mL) bottles, UPC 0 11169 00004 6, and 8 FL OZ (236 mL) bottles, UPC 0 11169 00008 4, The Oakhurst Co., Dist., Levittown, NY 11756.

by Ecometics, Inc.

Reason
CGMP Deviations: Products not manufactured under current good manufacturing practices.
Published
August 30, 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.