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.

37,143
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,799
Class I recallsReasonable probability of serious health consequences
24,349
Class II recallsTemporary or medically reversible health consequences
2,891
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/sierra-nevada-cheese-company-recalls-graziers-raw-milk-cheese-because-possible-health-riskPublished September 28, 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 II24,349
Class I9,799
Class III2,891
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,349
Class I9,799
Class III2,891
Not Yet Classified1

Showing 12,961–12,980 of 18,257 recalls

FDA Recall Terminated Historical recordClass II

Heparin Sodium, 1 USP Unit/2 mL (0.5 USP Units/mL) in 0.45% Sodium Chloride, Single-Dose Syringe, Hospital/Office Use Only, Rx Only, Cantrell Drug Co. 7321 Cantrell Rd. Little Rock, AR 72207, NDC 52533-148-16

by Cantrell Drug Company

Reason
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Published
December 21, 2016
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Glycopyrrolate 1 mg/5 mL (0.2 mg/mL) Injection Solution, 5 mL Single-Dose Syringe, For IV Use, Hospital/Office Use Only, Rx Only, Cantrell Drug Co. 7321 Cantrell Rd. Little Rock, AR 72207, NDC 52533-028-15

by Cantrell Drug Company

Reason
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Published
December 21, 2016
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Fentanyl Citrate 2 mcg/mL & Bupivacaine HCl 0.125% in 0.9% Sodium Chloride, 100 mL* Bag, Epidural Use Only, Single-Dose Bag, Hospital/Office Use Only, Rx Only, Cantrell Drug Company 7321 Cantrell Road Little Road, AR 72207, NDC 52533-080-75

by Cantrell Drug Company

Reason
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Published
December 21, 2016
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Fentanyl Citrate 2,500 mcg in 0.9% Sodium Chloride (10 mcg/mL) 250 mL* Bag, Single-Dose Bag, Rx Only, Cantrell Drug Company 7321 Cantrell Road Little Road, AR 72207, NDC 52533-024-61

by Cantrell Drug Company

Reason
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Published
December 21, 2016
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Fentanyl Citrate 1,500 mcg in 0.9% Sodium Chloride (10 mcg/mL) 150 mL Bag, Single-Dose Bag, Rx Only, Cantrell Drug Company 7321 Cantrell Road Little Road, AR 72207, NDC 52533-024-35

by Cantrell Drug Company

Reason
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Published
December 21, 2016
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Calcium Chloride, (1 g/10 mL) Injection Solution 10 mL, 10% Single-Dose Vial, Rx Only, Cantrell Drug Co. 7321 Cantrell Road Little Rock, AR 72207

by Cantrell Drug Company

Reason
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Published
December 21, 2016
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Calcium Chloride (20 mg/mL) in 0.9% Sodium Chloride 500 mL Bag, Rx Only, Single-Dose Bag Cantrell Drug Company 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-102-09

by Cantrell Drug Company

Reason
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Published
December 21, 2016
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Phenylephrine HCl 1 mg/10 mL (100 mcg/mL) in 0.9% Sodium Chloride, 10 mL Single-Dose Syringe, Rx Only Cantrell Drug Company 7321 Cantrell Rd Little Rock, AR 72207, NDC 52533-171-12

by Cantrell Drug Company

Reason
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Published
December 21, 2016
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Calcium Chloride 1 g/50 mL* Added to 5% Dextrose (20 mg/mL)*, Single-Dose Bag, Rx Only, Hospital/Office Use Only, Cantrell Drug Co. 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-175-37

by Cantrell Drug Company

Reason
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Published
December 21, 2016
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

Apple Tree Goat Dairy

Product
Apple Tree Goat Dairy French Herb Chevre, Net WT. 8 oz shrin…
Reason
Product may be contaminated with Listeria monocytogenes.
Published
December 21, 2016
Distribution
DC, MD, NJ, NY, PA and VA

View recall →

FDA Recall United States Terminated Historical recordClass I

Apple Tree Goat Dairy

Product
Apple Tree Goat Dairy FETA; Raw cultured goat milk; Aged 60…
Reason
Product may be contaminated with Listeria monocytogenes.
Published
December 21, 2016
Distribution
DC, MD, NJ, NY, PA and VA

View recall →

FDA Recall United States Terminated Historical recordClass I

Apple Tree Goat Dairy

Product
Apple Tree Goat Dairy Chevre, Net Wt. 8 oz. shrink wrap and…
Reason
Product may be contaminated with Listeria monocytogenes.
Published
December 21, 2016
Distribution
DC, MD, NJ, NY, PA and VA

View recall →

FDA Recall United States Terminated Historical recordClass I

Apple Tree Goat Dairy

Product
Apple Tree Goat Dairy, Cheddar; Raw cultured goat milk; Age…
Reason
Product may be contaminated with Listeria monocytogenes.
Published
December 21, 2016
Distribution
DC, MD, NJ, NY, PA and VA

View recall →

FDA Recall United States Terminated Historical recordClass I

Apple Tree Goat Dairy

Product
Apple Tree Goat Dairy Gouda; Net Wt. 8 oz. shrink wrap block…
Reason
Product may be contaminated with Listeria monocytogenes.
Published
December 21, 2016
Distribution
DC, MD, NJ, NY, PA and VA

View recall →

FDA Recall Terminated Historical recordClass II

USCG Boat Response Kit - Product Code 80-0353, North American Rescue

by North American Rescue LLC.

Reason
Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
Published
December 14, 2016
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Aid Backpack Kit - Product Code 85-0917, North American Rescue

by North American Rescue LLC.

Reason
Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
Published
December 14, 2016
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Mini Resupply Trauma Kit - Product Code 85-0835, North American Rescue

by North American Rescue LLC.

Reason
Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
Published
December 14, 2016
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Amphibious Trauma Kit - Product Code 85-0639, North American Rescue

by North American Rescue LLC.

Reason
Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
Published
December 14, 2016
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

K-9 Trauma Field Kit - Product Code 80-0211, 80-0304, 80-0209, 80-0210, 80-0300, 80-0301, North American Rescue

by North American Rescue LLC.

Reason
Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
Published
December 14, 2016
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Advance Trauma Kit - Product Code 85-0742, 85-0746, 85-0745, 85-0639, 85-0744, 85-0744, 85-0741, North American Rescue

by North American Rescue LLC.

Reason
Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
Published
December 14, 2016
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.