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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.

37,066
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

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 II24,313
Class I9,786
Class III2,876
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,313
Class I9,786
Class III2,876
Not Yet Classified2

Showing 3,961–3,980 of 17,805 recalls

FDA Recall Terminated Historical recordClass III

Clonidine Hydrochloride Tablets, USP, 0.3 mg, 100-count bottle, Rx Only, Manufactured by: UNICHEM LABORATORIES LTD. Pilerne Ind. Estate, Pilerne, Bardez, Goa 403 511, India Manufactured for: UNICHEM PHARMACEUTICALS (USA), INC. East Brunswick, NJ 08816. NDC# 29300-137-01

by UNICHEM PHARMACEUTICALS USA INC

Reason
Product mix-up:0.2 mg strength Clonidine Hydrochloride Tablets, USP in a 100-count bottle of 0.3 mg strength Clonidine Hydrochloride Tablets,
Published
September 28, 2022
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass III

Pepsico Inc

Product
Mountain Dew Major Melon Zero, 12 FL OZ (355mL) can, sold as…
Reason
The outer wraps match the liquid in the can (Zero Sugar - Mountain Dew Major Melon) however the primary package (can) is incorrect (Full Sugar Mountain Dew Major Melon). Product inside can matches the product/nutritional panel on the point-of-sale outer container wrap.
Published
September 28, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

PROPOFOL Injectable Emulsion, 1 g/100 mL (10 mg/mL), packaged in 100 mL glass fliptop vial (NDC 0409-4699-54) further packaged in a tray of 10 vials (NDC Carton: 0409-4699-24), Rx only, Distributed by Hospira, Inc., Lake Forest, IL 60045 USA

by Pfizer Inc.

Reason
Presence of particulate matter
Published
September 21, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets (Mixed Salts of a Single Entity Amphetamine Product), 15 mg, Rx Only, 100 tablets per bottle, Teva Pharmaceuticals USA, Inc. North Wales, PA 19454, NDC 0555-0777-02.

by Teva Pharmaceuticals USA Inc

Reason
Labeling: Label Error on Declared Strength; A sealed 100-count bottle labeled with 15 mg actually contained 100 tablets of 20 mg strength of the drug product.
Published
September 21, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Lisinopril 10 mg tablets, 30-count Blister Card, Rx Only, MFG: Lupin Pharma, Baltimore, MD Repackaged by: RemedyRepack Inc, Indiana PA. Original NDC# 68180-0980-03, Repackaged NDC# 70518-0468-00

by RemedyRePack Inc.

Reason
Presence of Foreign Substance: Foreign material (metal piece) embedded in one tablet.
Published
September 21, 2022
Distribution
Distributed to two direct accounts in PA…

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FDA Recall Terminated Historical recordClass II

Synergy Hand Sanitizer, Non-Sterile Solution to help reduce bacteria that can potentially cause disease, For use when soap and water are not available, Alcohol 80% Topical Solution, Antiseptic, 8.5 oz./ 250 mL bottles, Made and Distributed by: Superior Glove Works Ltd., 36 Vimy Street, Acton, Ontario, L7J 1S1, Canada, Made in Canada, UPC: 779406201594.

by SUPERIOR GLOVE WORKS, LTD.

Reason
CGMP Deviations: FDA analysis found product to contain acetaldehyde impurity and the Sum of All Impurities, above specification limits.
Published
September 21, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Lisinopril Tablets USP, 10 mg, 1000-count bottles, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202, Manufactured by: Lupin Limited, Nagpur- 441 108, India. NDC 68180-980-03

by Lupin Pharmaceuticals Inc.

Reason
Presence of Foreign Substance: Foreign material (metal piece) embedded in one tablet.
Published
September 21, 2022
Distribution
Nationwide

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FDA Recall Completed Historical recordClass II

QUAD-MIX 30MG/3MG/60MCG/0.2 Injectable, 10 ML vial, Rx only, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936.

by Carolina Infusion

Reason
Lack of Assurance of Sterility
Published
September 21, 2022
Distribution
Nationwide

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FDA Recall Completed Historical recordClass II

QUAD-MIX 30/2/60/0.15 Injectable, 5 ML vial, Rx only, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936.

by Carolina Infusion

Reason
Lack of Assurance of Sterility
Published
September 21, 2022
Distribution
Nationwide

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FDA Recall Completed Historical recordClass II

TRI-MIX 50/2.5/25 Injectable, 2 ML vial, Rx only, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936.

by Carolina Infusion

Reason
Lack of Assurance of Sterility
Published
September 21, 2022
Distribution
Nationwide

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FDA Recall Completed Historical recordClass II

TRI-MIX 30/2/40 Injectable, 10 ML vial, Rx only, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936.

by Carolina Infusion

Reason
Lack of Assurance of Sterility
Published
September 21, 2022
Distribution
Nationwide

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FDA Recall Completed Historical recordClass II

TRI-MIX 30/2/20 Injectable, 10 ML vial, Rx only, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936.

by Carolina Infusion

Reason
Lack of Assurance of Sterility
Published
September 21, 2022
Distribution
Nationwide

View recall →

FDA Recall Completed Historical recordClass II

TRI-MIX 30/1/60 Injectable, 5 ML vial, Rx only, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936.

by Carolina Infusion

Reason
Lack of Assurance of Sterility
Published
September 21, 2022
Distribution
Nationwide

View recall →

FDA Recall Completed Historical recordClass II

TRI-MIX 30/1/40 Injectable, 10 ML vial, Rx only, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936.

by Carolina Infusion

Reason
Lack of Assurance of Sterility
Published
September 21, 2022
Distribution
Nationwide

View recall →

FDA Recall Completed Historical recordClass II

TRI-MIX 30/1/20 Injectable, 5 ML vial, Rx only, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936.

by Carolina Infusion

Reason
Lack of Assurance of Sterility
Published
September 21, 2022
Distribution
Nationwide

View recall →

FDA Recall Completed Historical recordClass II

TRI-MIX 30/1/10 Injectable, 10 ML vial, Rx only, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936.

by Carolina Infusion

Reason
Lack of Assurance of Sterility
Published
September 21, 2022
Distribution
Nationwide

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FDA Recall Completed Historical recordClass II

TEST CYP/PROP (50:50) 100 MG/100 MG/ML Injectable, 12.6 ML vial, Rx only, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936.

by Carolina Infusion

Reason
Lack of Assurance of Sterility
Published
September 21, 2022
Distribution
Nationwide

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FDA Recall Completed Historical recordClass II

TEST CYP/DHEA (Sesame) 200 MG/2.5 MG/ML Injectable, 10 ML vial, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936.

by Carolina Infusion

Reason
Lack of Assurance of Sterility
Published
September 21, 2022
Distribution
Nationwide

View recall →

FDA Recall Completed Historical recordClass II

TEST CYP/DHEA (Sesame Oil) 100 MG/2.5 MG/ML Injection, 3 ML and 6 ML vials, Rx only, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936.

by Carolina Infusion

Reason
Lack of Assurance of Sterility
Published
September 21, 2022
Distribution
Nationwide

View recall →

FDA Recall Completed Historical recordClass II

TEST CYP (Grapeseed) 200 MG/ML Injectable, 10 ML vial, Rx only, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936.

by Carolina Infusion

Reason
Lack of Assurance of Sterility
Published
September 21, 2022
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.