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Recall totals

All FDA and USDA recalls in Public Health Trace, June 2012 to September 2026.

37,063

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/evergreen-fresh-sprouts-llc-recalls-broccoli-sprouts-because-possible-health-riskPublished September 10, 2026

Most affected stateHawaii 200 recalls mention this state

State: MP ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated September 11, 2026 ET

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

Recalls by class
Class	Recalls
Class II	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

FDA Recall Ongoing Historical recordClass II

Epinephrine-Lidocaine HCl 0.25 mg/mL and 7.5 mg/mL Preservative-Free 1mL Single-Use vials for Intraocular Injection, Imprimis NJOF, LLC. 1705 Route 46 West, unit 6B, Ledgewood, NJ 07852, NDC 71384-640-01

by Imprimis NJOF, LLC

Reason: Lack of Assurance of Sterility
Published: June 5, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

Tirzepatide 10 mg/0.5 mL Sterile Solution, 2 mL Multi-dose vial, Rx only, This is a Compounded Product By: Revive RX Pharmacy, 3831 Golf Dr A, Houston, TX 77018, internally assigned NDC 99000-9278-64

by Revive Rx LLC dba Revive Rx Pharmacy

Reason: Labeling: Label Mix-up - product labeled as tirzepatide contains testosterone cypionate
Published: June 5, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Zoledronic Acid Injection 5mg/100mL Sterile Solution, 100mL Single-Dose vials, Rx only, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, Made in India, NDC 55111-688-52

by Dr. Reddy's Laboratories, Inc.

Reason: Lack of Assurance of Sterility: Leaking vials
Published: June 5, 2024
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Cathflo activase (ALTEPLASE), 2mg vials, Rx only, Genentech Inc., South San Francisco, CA 94080, NDC 50242-041-64

by Genentech, Inc.

Reason: Lack of Assurance of Sterility: Deformed stoppers observed during filling operations for Cathflo Activase.
Published: June 5, 2024
Distribution: Nationwide

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FDA Recall United States Ongoing Historical recordClass II

Nutrition Corp

Product: Fresh N Lean brand Crustless Chicken Potato Pot Pie. Package…
Reason: Possible contamination with Listeria monocytogenes
Published: June 5, 2024
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Maribel's Sweets, Inc.

Product: 9. 25pc Mother s Day heart ganache box
Reason: Contains undeclared coconut.
Published: June 5, 2024
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Maribel's Sweets, Inc.

Product: 8. 16pc Mother s Day ganache box
Reason: Contains undeclared coconut.
Published: June 5, 2024
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Maribel's Sweets, Inc.

Product: 7. 7pc Mother s Day heart box
Reason: Contains undeclared coconut.
Published: June 5, 2024
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Maribel's Sweets, Inc.

Product: 6. Mother s Day love purse
Reason: Contains undeclared coconut.
Published: June 5, 2024
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Maribel's Sweets, Inc.

Product: 5. 9pc signature box
Reason: Contains undeclared coconut.
Published: June 5, 2024
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Maribel's Sweets, Inc.

Product: 4. 6pc signature ganache box
Reason: Contains undeclared coconut.
Published: June 5, 2024
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Maribel's Sweets, Inc.

Product: 3. 4pc ganache box
Reason: Contains undeclared coconut.
Published: June 5, 2024
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Maribel's Sweets, Inc.

Product: 2. 2pc signature Ganache box
Reason: Contains undeclared coconut.
Published: June 5, 2024
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Maribel's Sweets, Inc.

Product: 1. 2pc Ganache tote box
Reason: Contains undeclared coconut.
Published: June 5, 2024
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Vasopressin Injection, USP, 200 Units per 10 mL (20 Units per mL), 10 mL Multiple-Dose Vial, Rx only, For Intravenous Infusion, American Regent, Inc., Shirley, NY 11967, NDC 0517-1030-01

by American Regent, Inc.

Reason: Subpotent product in addition to having out-of-specification results for impurities.
Published: May 29, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Haloperidol decanoate Injection 50mg/mL, packaged in a) 1 mL Single-Dose Vials (NDC 70069-381-01) and b) 10 1mL Single-Dose Vials (NDC 70069-381-10), Rx only, Manufactured for: Somerset Therapeutics, LLC, Hollywood, FL 33024, Made in India.

by SOMERSET THERAPEUTICS LLC

Reason: Presence of Foreign Substance: This oil based product may contain trace amounts of water for injection (WFI).
Published: May 29, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass III

Sirolimus Tablets 1mg Tablets 100-count bottle, Rx Only, Distributed by: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, Made in India, NDC 55111-653-01

by Dr. Reddy's Laboratories, Inc.

Reason: Failed Impurities/Degradation Specifications
Published: May 29, 2024
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass III

Natural Waters of Viti Limited

Product: Fiji Natural Artesian Water 500 mL (24 pack) Case UPC Code:…
Reason: Firm testing revealed Manganese in addition to three bacterial genera.
Published: May 29, 2024
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Colonna Brothers Inc.

Product: Supreme Tradition brand and Marcum brand ground cinnamon. Pa…
Reason: Elevated lead levels in cinnamon
Published: May 29, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Meijer Magnesium Citrate Saline Laxative Oral Solution Dye Free, Sugar Free Grape, 10 fl. oz bottle, Distributed by: Meijer Distribution Inc., Grand Rapids,MI 49544, NDC 79481-0034-9

by Pharma Nobis LLC

Reason: Microbial Contamination of Non-Sterile Products - Presence of Acetobacter nitrogenifigens bacteria
Published: May 22, 2024
Distribution: Nationwide

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Data last updated: September 11, 2026 ET

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.