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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.

37,139
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/deanos-pasta-issue-allergy-alert-undeclared-lobster-pear-and-pecorino-triangoli-ravioliPublished September 24, 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.

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Recalls announced by month (Year to date)

A chart of recalls grouped by month.

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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 11,941–11,960 of 17,237 recalls

FDA Recall United States Terminated Historical recordClass II

Brownwood Farms

Product
Brownwood Farms Apple Riesling Salsa. 21oz glass bottles an…
Reason
Products contain yellow#5 ingredients not declared on the label.
Published
December 28, 2016
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Brownwood Farms

Product
Brownwood Farms BBQ Mustard Glaze. 11oz glass bottles and 1…
Reason
Products contain soy ingredients not declared on the label.
Published
December 28, 2016
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Brownwood Farms

Product
Brownwood Farms Cherry BBQ Sauce. 21oz glass bottles, 1 gal…
Reason
Products contain soy ingredients not declared on the label.
Published
December 28, 2016
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Brownwood Farms

Product
Brownwood Farms Yankee Bourbon BBQ Sauce. 19oz glass bottle…
Reason
Products contain soy ingredients not declared on the label.
Published
December 28, 2016
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Chaos and Pain

Product
CANNIBAL FEROX AMPED, FACE-MELTING NOOTROPIC, PRE-WORKOUT EN…
Reason
Product was analyzed and found to contain 1,3- dimethylbutylamine which was not declared on the label and is a prohibited substance.
Published
December 28, 2016
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

NATURECOM INC

Product
DMAA (1,3-Dimethylamylamine) Net Weight 500g Product is p…
Reason
Naturecom dba NutriVitaShop is recalling DMAA net weight 500 g because there may be presence of 1,3-dimethylamylamine.
Published
December 28, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Methylprednisolone Tablets, USP, 16 mg, 50-count bottles, Rx only, Manufactured by Jubilant Cadista Pharmaceuticals Inc., Salisbury, MD 21801, NDC 59746-003-14.

by Jubilant Cadista Pharmaceuticals, Inc.

Reason
Labeling: Incorrect or Missing Lot and/or Exp Date: incorrect expiration date of 02/0218 is printed on the container label instead of the correct expiration date of 02/2018.
Published
December 21, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Succinylcholine Chloride 200 mg/10 mL Injection Solution 10 mL (20 mg/mL) ,Single-Dose Syringe Injection Solution, For Slow IV Use Only ,Rx Only, Cantrell Drug Company 7321 Cantrell Rd Little Rock, AR 72207, NDC 52533-067-12

by Cantrell Drug Company

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

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FDA Recall Terminated Historical recordClass II

Ropivacaine HCl 0.25% in 0.9% Sodium Chloride, 100 mL Bag, Epidural Use Only, Rx Only, Cantrell Drug Co. 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-185-75

by Cantrell Drug Company

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

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FDA Recall Terminated Historical recordClass II

Rocuronium Bromide 50 mg/5 mL Injection Solution, 5 mL (10 mg/mL) Single-Dose Syringe, Injection Solution For Slow IV Use, Rx Only, Cantrell Drug Co. 7321 Cantrell Rd. Little Rock, AR 72207, NDC 52533-064-15

by Cantrell Drug Company

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

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FDA Recall Terminated Historical recordClass II

Oxytocin 30 USP Units Added to 0.9% Sodium Chloride, 500 mL Bag, Single-Dose Bag, Injection Solution for IV Use Only, Rx Only, Cantrell Drug Company 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-056-30

by Cantrell Drug Company

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

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FDA Recall Terminated Historical recordClass II

Neostigmine Methylsulfate 5 mg/5 mL Injection Solution, 5 mL (1 mg/mL) Single-Dose Syringe, For Slow IV Use, Rx Only, Cantrell Drug Co. 7321 Cantrell Rd. Little Rock, AR 72207, NDC 52533-046-15

by Cantrell Drug Company

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

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FDA Recall Terminated Historical recordClass II

Morphine Sulfate 1 mg/mL in 0.9% Sodium Chloride, 100 mL Bag, Single-Dose Bag, Rx Only, Cantrell Drug Co. 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-160-75

by Cantrell Drug Company

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

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FDA Recall Terminated Historical 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

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FDA Recall Terminated Historical 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 Terminated Historical 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

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FDA Recall Terminated Historical 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

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FDA Recall Terminated Historical 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

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FDA Recall Terminated Historical 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

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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 →

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.