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.

37,497
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,881
Class I recallsReasonable probability of serious health consequences
24,543
Class II recallsTemporary or medically reversible health consequences
2,935
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 2,098 recalls
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/family-farmstead-dairy-announces-recall-all-cheddar-cheese-products-because-possible-health-riskPublished November 10, 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 II24,543
Class I9,881
Class III2,935
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,543
Class I9,881
Class III2,935
Not Yet Classified2

Showing 15,781–15,800 of 21,347 recalls

FDA Recall TerminatedTerminated: April 29, 2020Historical recordClass II

Midazolam HCl 50 mg/50 mL in 0.9% Sodium Chloride (1 mg/mL), Single-Dose Syringe, Hospital/Office Use Only, Rx Only, Cantrell Drug Co. 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-001-04

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 TerminatedTerminated: April 29, 2020Historical recordClass II

Lidocaine HCl 1%, 10 mL Syringe, Hospital/Office Use Only, Rx Only, Cantrell Drug Co. 7321 Cantrell Rd. 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 TerminatedTerminated: April 29, 2020Historical recordClass II

Hydromorphone HCl 1 mg/mL in 0.9% Sodium Chloride 30 mL PCA Vial (1 mg/mL), Single-Dose Injection Solution For Slow IV Use, Rx Only, Cantrell Drug Co. 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-006-10

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 TerminatedTerminated: April 29, 2020Historical recordClass II

HYDROmorphone HCl 50 mg/50 mL in 0.9% Sodium Chloride (1 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Co. 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-006-04

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 TerminatedTerminated: April 29, 2020Historical recordClass II

HYDROmorphone HCl 6 mg/30 mL in 0.9% Sodium Chloride (0.2 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Co. 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-002-03

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 TerminatedTerminated: April 29, 2020Historical recordClass II

Heparin Sodium 5,000 USP Units Added to 0.9% Sodium Chloride 1,000 mL* Bag (5 USP units/mL), Single-Dose Bag.,Hospital/Office Use Only, Injection Solution For IV Use, Rx Only, Cantrell Drug Company 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-097-24

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 TerminatedTerminated: April 29, 2020Historical 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 TerminatedTerminated: April 29, 2020Historical 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 TerminatedTerminated: April 29, 2020Historical 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 TerminatedTerminated: April 29, 2020Historical 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 TerminatedTerminated: April 29, 2020Historical 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 TerminatedTerminated: April 29, 2020Historical 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 TerminatedTerminated: April 29, 2020Historical 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 TerminatedTerminated: April 29, 2020Historical 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 TerminatedTerminated: April 29, 2020Historical 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 TerminatedTerminated: February 28, 2017Historical recordClass II

Cargill, Inc Corporate Headquarters

Product
refyne Artificially Flavored BUTTER FLAVORED OIL, NET CONTEN…
Reason
Products contain an excessive amount of TBHQ (tert-Butylhydroquinone) and DMPS (dimethyl polysiloxane).
Published
December 21, 2016
Distribution
Product was shipped to the following sta…

View recall →

FDA Recall United States TerminatedTerminated: February 28, 2017Historical recordClass II

Cargill, Inc Corporate Headquarters

Product
Crisco PROFESSIONAL Liquid Butter Alternative, SALTED FOR A…
Reason
Products contain an excessive amount of TBHQ (tert-Butylhydroquinone) and DMPS (dimethyl polysiloxane).
Published
December 21, 2016
Distribution
Product was shipped to the following sta…

View recall →

FDA Recall United States TerminatedTerminated: February 28, 2017Historical recordClass II

Cargill, Inc Corporate Headquarters

Product
Beyond PREMIUM LIQUID BUTTER ALTERNATIVE ,ARTIFICIALLY FLAVO…
Reason
Products contain an excessive amount of TBHQ (tert-Butylhydroquinone) and DMPS (dimethyl polysiloxane).
Published
December 21, 2016
Distribution
Product was shipped to the following sta…

View recall →

FDA Recall United States TerminatedTerminated: February 28, 2017Historical recordClass II

Cargill, Inc Corporate Headquarters

Product
MONARCH LIQUID BUTTER ALTERNATIVE, ARTIFICIALLY FLAVORED ,NE…
Reason
Products contain an excessive amount of TBHQ (tert-Butylhydroquinone) and DMPS (dimethyl polysiloxane).
Published
December 21, 2016
Distribution
Product was shipped to the following sta…

View recall →

FDA Recall United States TerminatedTerminated: February 28, 2017Historical recordClass II

Cargill, Inc Corporate Headquarters

Product
QUALI FRY PREMIUM BUTTERY PAN AND GRILL, ARTIFICIALLY FLAVOR…
Reason
Products contain an excessive amount of TBHQ (tert-Butylhydroquinone) and DMPS (dimethyl polysiloxane).
Published
December 21, 2016
Distribution
Product was shipped to the following sta…

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.