Public Health Trace

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

State: RI ×
Clear all

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

Timeline Classification Table

Metric

Time range

Group by

View

Recalls announced by month (Year to date)

Download CSV

Source: FDA and USDA public dataLast updated September 12, 2026 ET

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

Recalls by class
Class	Recalls
Class II	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

Recalls by class
Class	Recalls
Class II	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

FDA Recall United States Terminated Historical recordClass II

Cargill, Inc Corporate Headquarters

Product: PROSANTE TSOYFLR 5P MNCD 50LB BG/21P, PROSANTE TSOYFLR 5P MN…
Reason: Products with a gluten free claim may contain gluten levels above 20 ppm.
Published: May 10, 2023
Distribution: Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Cargill, Inc Corporate Headquarters

Product: PROSANTE TSOYFLR 3P MNCD 50LB BG, paper bag
Reason: Products with a gluten free claim may contain gluten levels above 20 ppm.
Published: May 10, 2023
Distribution: Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Cargill, Inc Corporate Headquarters

Product: PROSANTE TSOYFLR 10P MNCD 50LB BG, paper bag
Reason: Products with a gluten free claim may contain gluten levels above 20 ppm.
Published: May 10, 2023
Distribution: Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Cargill, Inc Corporate Headquarters

Product: PROSANTE TVGPTN 10B MNCD 25LB BG/40P, PROSANTE TVGPTN 10B MN…
Reason: Products with a gluten free claim may contain gluten levels above 20 ppm.
Published: May 10, 2023
Distribution: Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Cargill, Inc Corporate Headquarters

Product: PROSANTE TVGPTN 3018B FLK 50LB BG, paper bag
Reason: Products with a gluten free claim may contain gluten levels above 20 ppm.
Published: May 10, 2023
Distribution: Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Cargill, Inc Corporate Headquarters

Product: PROSANTE TSOYFLR 3014P FLK 50LB BG, paper bag
Reason: Products with a gluten free claim may contain gluten levels above 20 ppm.
Published: May 10, 2023
Distribution: Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Cargill, Inc Corporate Headquarters

Product: PROSANTE TVGPTN 3014B FLK 50LB BG, paper bag
Reason: Products with a gluten free claim may contain gluten levels above 20 ppm.
Published: May 10, 2023
Distribution: Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Cargill, Inc Corporate Headquarters

Product: PROLIA SOY FLR 200/20 STD BLK, PROLIA SOY FLR 200/70 STD BLK…
Reason: Products with a gluten free claim may contain gluten levels above 20 ppm.
Published: May 10, 2023
Distribution: Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Cargill, Inc Corporate Headquarters

Product: PROSANTE TSOYFLR 3018P FLK 50LB BG, PROSANTE TSOYFLR 3018P F…
Reason: Products with a gluten free claim may contain gluten levels above 20 ppm.
Published: May 10, 2023
Distribution: Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Cargill Cocoa & Chocolate, Inc.

Product: Wilbur¿ Dark Chocolate Covered Cashews Net Wt.16 oz (1 LB) 4…
Reason: Undeclared peanut
Published: May 10, 2023
Distribution: Distributed to 6 consumers in MN, NJ, OH…

View recall →

FDA Recall Terminated Historical recordClass II

Fyremadel (ganirelix acetate) injection, 250 mcg/0.5 mL, One Single Dose Sterile Prefilled Syringe 0.5 mL, For Subcutaneous Use, Rx Only, Sterile, Distributor: Ferring Pharmaceuticals Inc., Parsippany, NJ 07054, USA, NDC 55566-1010-1

by Sun Pharmaceutical Industries Ltd.

Reason: Presence of Particulate Matter: A piece of glass was found in a prefilled syringe.
Published: May 3, 2023
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Oxytocin 30 units added to 0.9% Sodium Chloride 500 mL, Rx Only, Single Dose Container, SCA Pharmaceuticals, Windsor, CT 06095, NDC# 70004-085-44

by SCA Pharmaceuticals

Reason: Subpotent Drug: Out of specification results for low potency was obtained.
Published: May 3, 2023
Distribution: Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Tadalafil Tablets, USP 5 mg, 30-count bottles, Rx Only, Repackaged By: Northwind Pharmaceuticals, Indianapolis, IN 46203. NDC 51655-487-52

by Northwind Pharmaceuticals LLC

Reason: CGMP Deviations
Published: May 3, 2023
Distribution: Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Tadalafil Tablets, USP 20 mg, packaged in a) 6-count bottles (NDC 51655-473-87), and b) 15-count bottles (NDC 51655-473-54), Rx Only, Repackaged By: Northwind Pharmaceuticals, Indianapolis, IN 46203.

by Northwind Pharmaceuticals LLC

Reason: CGMP Deviations
Published: May 3, 2023
Distribution: Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Glimepiride Tablets, USP 4mg, packaged in a) 30-count bottles (NDC 51655-120-52), and b) 90-count bottles (NDC 51655-120-26), Rx Only, Repackaged By: Northwind Pharmaceuticals, Indianapolis, IN 46203.

by Northwind Pharmaceuticals LLC

Reason: CGMP Deviations
Published: May 3, 2023
Distribution: Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Glimepiride Tablets, USP 2mg, packaged in a) 30-count bottles (NDC 51655-383-52), and b)90-count bottles (NDC 51655-383-26), Rx Only, Repackaged By: Northwind Pharmaceuticals, Indianapolis, IN 46203.

by Northwind Pharmaceuticals LLC

Reason: CGMP Deviations
Published: May 3, 2023
Distribution: Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Doxazosin Tablets, USP, 4mg, 30-count bottles, Rx Only, Repackaged By: Northwind Pharmaceuticals, Indianapolis, IN 46203. NDC 51655-109-52

by Northwind Pharmaceuticals LLC

Reason: CGMP Deviations
Published: May 3, 2023
Distribution: Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

BusPIRone Hydrochloride Tablets USP, 7.5 mg, 30-count bottles, Rx Only, Repackaged By: NOrthwind Pharmaceuticals, Indianapolis, IN 46203. NDC 51655-511-52

by Northwind Pharmaceuticals LLC

Reason: CGMP Deviations
Published: May 3, 2023
Distribution: Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Atorvastatin Calcium Tablets, USP, 10 mg, 30-count bottles, Rx Only, Repackaged By: Northwind Pharmaceuticals, Indianapolis, IN 46203. NDC 51655-946-52

by Northwind Pharmaceuticals LLC

Reason: CGMP Deviations
Published: May 3, 2023
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Avicel DG, MCC/Dibasic Calcium Phosphate, 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; Manufactured in 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: May 3, 2023
Distribution: Nationwide

View recall →

Data last updated: September 12, 2026 ET

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.