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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 October 2026.

37,343
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,860
Class I recallsReasonable probability of serious health consequences
24,450
Class II recallsTemporary or medically reversible health consequences
2,901
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 2,095 recalls
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/vitality-works-inc-recalls-365-whole-foods-market-ashwagandha-capsules-sold-nationwide-due-potentialPublished October 30, 2026
Most affected stateHawaii 200 recalls mention this state

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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)

  • 1,853 recalls have been announced year to date.
  • Oct 2026 was 45% lower than the previous complete period (Sep 2026: 209).
  • The highest complete period was Jun 2026 (300).
Recalls by class

A bar chart of the total number of recalls in this dataset by recall class.

Recalls by class
ClassRecalls
Class II24,450
Class I9,860
Class III2,901
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,450
Class I9,860
Class III2,901
Not Yet Classified2

Showing 3,441–3,460 of 22,707 recalls

FDA Recall United States TerminatedTerminated: September 5, 2024Historical recordClass II

Greco Sidari

Product
Norpaco GARLIC STUFF OLIVE 1/7.5# SUPC/ITEM # 3461
Reason
The food was not held at an appropriate temperature. The holding temperature could affect spoilage and potentially support pathogen growth.
Published
February 14, 2024
Distribution
OH, NY & PA

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FDA Recall United States TerminatedTerminated: September 5, 2024Historical recordClass II

Greco Sidari

Product
RESER'S POTATOE POTATOES MASHED RED SKN 4/5# SUPC/ITEM # 326…
Reason
The food was not held at an appropriate temperature. The holding temperature could affect spoilage and potentially support pathogen growth.
Published
February 14, 2024
Distribution
OH, NY & PA

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FDA Recall TerminatedTerminated: September 18, 2024Historical recordClass I

Zenzedi (Dextroamphetamine Sulfate) CII Tablets, USP, 30 mg, 30-count bottle, Rx only, Mfd. for: Arbor Pharmaceuticals, LLC., Atlanta, Georgia, 30328, NDC 24338-856-03

by Azurity Pharmaceuticals, Inc.

Reason
Labeling: Label Mix-up
Published
February 7, 2024
Distribution
Nationwide

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FDA Recall OngoingHistorical recordClass II

Hydrogen Peroxide Oral Rinse, Significantly Reduces Bacteria, Fresh Mint Flavor, Alcohol Free, a)16 fl. oz. (473 mL) bottle, NDC 59883-202-16, UPC 3 59883 00009 7); b) 64 fl. oz. (1.89 L) bottle, NDC 59883-202-64; c) 128 fl. oz. (1 gal) 3.78L bottle, NDC 59883-202-28, UPC 3 59883 00007 3), Manufactured by: Den-Mat Holdings, LLC, Lompoc, CA 93436.

by Den-Mat Holdings, LLC

Reason
CGMP Deviations: products may not conform to the labeled specifications.
Published
February 7, 2024
Distribution
Nationwide

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FDA Recall OngoingHistorical recordClass II

OralProCare medicated lip treatment, Net Wt 9.9 g (0.35 oz) tube, Ethyl alcohol 6.0% Antibacterial, Manufactured by: Den-Mat Holdings, LLC, Lompoc, CA, 93436, USA, NDC 59883-500-01, UPC: 3 59883 00000 4.

by Den-Mat Holdings, LLC

Reason
CGMP Deviations: products may not conform to the labeled specifications.
Published
February 7, 2024
Distribution
Nationwide

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FDA Recall TerminatedTerminated: September 30, 2024Historical recordClass II

Rifampin Capsules USP, 150 mg, 30 Capsules (3 x 10) unit doses per carton, Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217. NDC Carton: 60687-575-21; NDC Unit Dose: 60687-575-11

by Amerisource Health Services LLC

Reason
Failed Impurities/Degradation Specification.
Published
February 7, 2024
Distribution
Nationwide

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FDA Recall OngoingHistorical recordClass I

VANCOmycin HCl PF 1.5g added to 0.9% Sodium Chloride 250 mL IV bag, Item F3208, for IV use only; Leiters 13796 Compark Blvd Englewood, CO 80112; NDC 71449-029-68.

by Denver Solutions, LLC DBA Leiters Health

Reason
Superpotent Drug: semi-automated IV bag filling system can malfunction and provide a double dose of drug product to IV bags.
Published
February 7, 2024
Distribution
Nationwide

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FDA Recall OngoingHistorical recordClass I

VANCOmycin HCl PF 1.25g added to 0.9% Sodium Chloride 250 mL IV bag, Item F3206, for IV use only; Leiters 13796 Compark Blvd Englewood, CO 80112; NDC 71449-028-68.

by Denver Solutions, LLC DBA Leiters Health

Reason
Superpotent Drug: semi-automated IV bag filling system can malfunction and provide a double dose of drug product to IV bags.
Published
February 7, 2024
Distribution
Nationwide

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FDA Recall OngoingHistorical recordClass I

PHENYLephrine HCl 40 mg per 250 mL 0.9% Sodium Chloride (160 mcg per mL), Item F3352, for IV use only; Leiters 13796 Compark Blvd Englewood, CO 80112; NDC 71449-150-82.

by Denver Solutions, LLC DBA Leiters Health

Reason
Superpotent Drug: semi-automated IV bag filling system can malfunction and provide a double dose of drug product to IV bags.
Published
February 7, 2024
Distribution
Nationwide

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FDA Recall OngoingHistorical recordClass I

PHENYLephrine HCl 20 mg per 250 mL 0.9% Sodium Chloride (80 mcg per mL), Item F3360, for IV use only; Leiters 13796 Compark Blvd Englewood, CO 80112; NDC 71449-148-94.

by Denver Solutions, LLC DBA Leiters Health

Reason
Superpotent Drug: semi-automated IV bag filling system can malfunction and provide a double dose of drug product to IV bags.
Published
February 7, 2024
Distribution
Nationwide

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FDA Recall OngoingHistorical recordClass I

FentaNYL citrate PF, 2500 mcg per 250 mL 0.9% Sodium Chloride (10 mcg per mL), Item F3342, for IV use only; Leiters 13796 Compark Blvd Englewood, CO 80112; NDC 71449-072-82.

by Denver Solutions, LLC DBA Leiters Health

Reason
Superpotent Drug: semi-automated IV bag filling system can malfunction and provide a double dose of drug product to IV bags.
Published
February 7, 2024
Distribution
Nationwide

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FDA Recall OngoingHistorical recordClass I

FentaNYL citrate PF, 1000 mcg per 100 mL 0.9% Sodium Chloride (10 mcg per mL), Item F3355, for IV use only; Leiters 13796 Compark Blvd Englewood, CO 80112; NDC 71449-072-41.

by Denver Solutions, LLC DBA Leiters Health

Reason
Superpotent Drug: semi-automated IV bag filling system can malfunction and provide a double dose of drug product to IV bags.
Published
February 7, 2024
Distribution
Nationwide

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FDA Recall OngoingHistorical recordClass II

Budesonide Extended-Release Tablets 9mg, 30-count bottle, Rx Only, Manufactured by: Actavis Laboratories FL, Inc., Fort Lauderdale, FL 33314 USA, Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054 USA, NDC 0591-2510-30

by Teva Pharmaceuticals USA, Inc

Reason
Failed Dissolution Specifications
Published
February 7, 2024
Distribution
Nationwide

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FDA Recall TerminatedTerminated: December 27, 2024Historical recordClass II

Cefixime for Oral Suspension 100mg/5mL, 50 mL bottle, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, Maryland 21202, Manufactured by:Lupin Limited, Mandideep 462 046 INDIA, NDC 68180-405-01

by Lupin Pharmaceuticals Inc.

Reason
Failed Impurities/Degradation Specifications
Published
February 7, 2024
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: July 16, 2024Historical recordClass II

8TH AVE PHARMACY

Product
Notoginseng Formula Special Gout Granule; 100% Natural; 8 G…
Reason
Product contains undeclared Diclofenac and Dexamethasone Acetate
Published
February 7, 2024
Distribution
Multiple states

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FDA Recall United States TerminatedTerminated: July 5, 2024Historical recordClass I

HY SUCCESS INC.

Product
Fat Choy Kee Dried Longan
Reason
Contains undeclared sulfites
Published
February 7, 2024
Distribution
Indiana, Missouri, Ohio, Pennsylvania, F…

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FDA Recall United States TerminatedTerminated: March 26, 2024Historical recordClass III

Nestle Product Technology Center - Nestle Health Science

Product
Solgar, Triple Strength, Shellfish -Free, Glucosamine Chondr…
Reason
Nestle Health Science has initiated a recall of Solgar Glucosamine Chondroitin, 120 Tablets, in Glass bottle, 12 bottles per case because of error during packaging in which a A Megasorb B-Complex product was filled into bottles labeled as Glucosamine_Chondroitin MSM.
Published
February 7, 2024
Distribution
The recalled product was distributed to…

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FDA Recall United States TerminatedTerminated: December 17, 2025Historical recordClass II

Benny Ts Vesta Inc dba Vesta Firey Gourmet Toppings

Product
the original BENNY T'S VESTA DRY HOT SAUCE VERY HOT NET WT.…
Reason
The firm was notified by the North Carolina Dept of Agriculture and Consumer Services that the product labeling does not include wheat and other ingredient common names in the ingredient statement.
Published
February 7, 2024
Distribution
Product was shipped to the following sta…

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FDA Recall United States TerminatedTerminated: December 17, 2025Historical recordClass II

Benny Ts Vesta Inc dba Vesta Firey Gourmet Toppings

Product
the original BENNY T'S VESTA DRY HOT SAUCE SCORPION NWT WT.…
Reason
The firm was notified by the North Carolina Dept of Agriculture and Consumer Services that the product labeling does not include wheat and other ingredient common names in the ingredient statement.
Published
February 7, 2024
Distribution
Product was shipped to the following sta…

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FDA Recall United States TerminatedTerminated: December 17, 2025Historical recordClass II

Benny Ts Vesta Inc dba Vesta Firey Gourmet Toppings

Product
the original BENNY T'S VESTA DRY HOT SAUCE REAPER NET WT. 1.…
Reason
The firm was notified by the North Carolina Dept of Agriculture and Consumer Services that the product labeling does not include wheat and other ingredient common names in the ingredient statement.
Published
February 7, 2024
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.

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