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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.

37,061
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 recallhttps://www.fsis.usda.gov/recalls-alerts/el-eden-import-distributor-corp-recalls-ineligible-pork-cracklings-products-importedPublished September 9, 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 1,921–1,940 of 17,805 recalls

FDA Recall United States Terminated Historical recordClass II

Sri Lakshmi Narasimhar Overseas

Product
Bliss Tree Moringa Butter Murukku 400g UPC:8906087452836. Pa…
Reason
Undeclared milk
Published
September 25, 2024
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Sri Lakshmi Narasimhar Overseas

Product
Bliss Tree Millet Butter Ribbon Pakoda 200g UPC:890608745162…
Reason
Undeclared milk
Published
September 25, 2024
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Sri Lakshmi Narasimhar Overseas

Product
Bliss Tree Millet Butter Murukku 200g UPC:8906087451631. Pac…
Reason
Undeclared sesame and milk
Published
September 25, 2024
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Sri Lakshmi Narasimhar Overseas

Product
Bliss Tree Ragi Butter Murukku 200g UPC:8906087451754. Packa…
Reason
Undeclared milk
Published
September 25, 2024
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Just Right 5000, 1.1% Sodium Fluoride, Candy Apple Flavor, Net Wt. 3.4oz (97g), Rx Only, Manufactured for Elevate Oral Care, LLC in the U.S.A with imported pump, 346 Pike Rd, Suite 5, West Palm Beach, FL 33411, NDC 57511-002-1

by Elevate Oral Care

Reason
LABELING: LABEL MIX-UP.
Published
September 18, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

BARRIER THERAPY SKIN PROTECTANT CREAM (1% colloidal oatmeal), 10 FL OZ/296 ML- tube, Distributed By: Prequel, LOS ANGELES, CA 90069. UPC 8 10129 11007 4

by PREQUEL SKIN

Reason
Microbial contamination of non-sterile Products -
Published
September 18, 2024
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

American Outdoor Products, Inc.

Product
American Outdoor Products - Astronaut Strawberries, packaged…
Reason
Elevated levels of lead
Published
September 18, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

TIRZEPATIDE 60 mg/3mL (20/mg/mL), Rx Only, 3mL Multiple Dose Vial, Mfd by: ProRx Exton, PA, 19341, NDC 84139-210-02

by ProRx LLC

Reason
Lack of Assurance of Sterility
Published
September 11, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

TIRZEPATIDE 20 mg/2mL (10/mg/mL), Rx Only, 2mL Multiple Dose Vial, Mfd by: ProRx Exton, PA, 19341, NDC 84139-210-01

by ProRx LLC

Reason
Lack of Assurance of Sterility
Published
September 11, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Semaglutide / Cyanocobalamin Injection: 2.5/0.5 mg/mL, 2 mL Multiple Dose Vial, Compounded Rx Product, ProRX 267-565-7008, NDC 84139-225-02

by ProRx LLC

Reason
Lack of Assurance of Sterility
Published
September 11, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

SEMAGLUTIDE 10mg/4mL (2.5mg/mL), 4 mL Multiple Dose Vial, Rx Only, Compounded Drug, Mfd by: ProRX Exton, PA19341, NDC 84139-225-04

by ProRx LLC

Reason
Lack of Assurance of Sterility
Published
September 11, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

SEMAGLUTIDE 5mg/2mL (2.5mg/mL), Rx Only 2 mL Multiple Dose Vial, Rx Only, Compounded Drug, Mfd by: ProRX Exton, PA19341, NDC 84139-225-01

by ProRx LLC

Reason
Lack of Assurance of Sterility
Published
September 11, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Tirzepatide 2 mL (10 mg/mL) and 20 mg/mL, 2mL Multidose SC Injection vials, Compounded Rx Product, ProRx 267-565-7008, NDC 84139-210-01

by ProRx LLC

Reason
Lack of Assurance of Sterility
Published
September 11, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Semaglutide, 2 mL (2.5mg/mL), Compounded RX Product, Multidose SC inj, glass vial, ProRx, 267-565-7008, NDC 84139-225-01

by ProRx LLC

Reason
Lack of Assurance of Sterility
Published
September 11, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass I

Heparin (Heparin Sodium in 0.9% Sodium Chloride Injection), 2,000 units per 1,000 mL (2 units/mL), 1000 mL Sterile Single Dose Container, Rx Only, Baxter USA, NDC 0338-0433-04

by Baxter Healthcare Corporation

Reason
Microbial Contamination of Sterile Products; out of limit results obtained for endotoxin testing.
Published
September 11, 2024
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Unilever North America Supply Chain Company, LLC

Product
Popsicle Jolly Rancher Frozen Confection Pop Net Wt 2.71 FL…
Reason
Undeclared milk
Published
September 11, 2024
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Cefixime for Oral Suspension USP, 100 mg/5 mL, 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
Subpotent Drug- An out of specification ( OOS ) result observed in assay test during 18-month long term stability study.
Published
September 4, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

IBU Ibuprofen Tablets, USP, 400 mg, Rx Only, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, Made in India, a) NDC 55111-682-01 - 100 Tablets per bottle, b) NDC 55111-682-05 - 500 Tablets per bottle.

by Dr. Reddy's Laboratories, Inc.

Reason
Failed impurities/degradation specifications: results for unknown impurity, were 0.13% and 0.11% respectively, exceeding the 0.10% specification limit.
Published
September 4, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

IBU Ibuprofen Tablets, USP, 600 mg, Rx Only, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, Made in India, a)NDC 55111-683-01 - 100 Tablets per bottle, b)NDC 5511-683-05 - 500 Tablets per bottle.

by Dr. Reddy's Laboratories, Inc.

Reason
Failed impurities/degradation specifications: results for unknown impurity, were 0.13% and 0.11% respectively, exceeding the 0.10% specification limit.
Published
September 4, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

IBU Ibuprofen Tablets, USP, 800 mg, Rx Only, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, Made in India, a)NDC 55111-684-01 - 100 Tablets per bottle, b)NDC 55111-684-05 - 500 Tablets per bottle.

by Dr. Reddy's Laboratories, Inc.

Reason
Failed impurities/degradation specifications: results for unknown impurity, were 0.13% and 0.11% respectively, exceeding the 0.10% specification limit.
Published
September 4, 2024
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.