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Recall totals

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

37,118

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,793

Class I recallsReasonable probability of serious health consequences

24,343

Class II recallsTemporary or medically reversible health consequences

2,887

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/gf-blends-recalls-truly-aip-all-purpose-flour-and-bread-mix-and-eat-gangster-flat-bread-pizza-mixPublished September 18, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 20, 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	24,343
Class I	9,793
Class III	2,887
Not Yet Classified	1

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Recalls by class
Class	Recalls
Class II	24,343
Class I	9,793
Class III	2,887
Not Yet Classified	1

FDA Recall Terminated Historical recordClass II

Estradiol 18mg pellet, 1 count (NDC 69761-018-01), 6 count (NDC 69761-018-06), 12 count (NDC 69761-018-12), and 30 count (NDC 69761-018-30) vials, Rx Only, Qualgen, LLC, Edmond, OK 73013

by Qualgen, LLC

Reason: Lack of Assurance of Sterility
Published: November 14, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Estradiol 10mg pellet, 1 count (NDC 69761-010-01), 6 count (NDC 69761-010-06), 12 count (NDC 69761-010-12), and 30 count (NDC 69761-010-30) vials, Rx Only, Qualgen, LLC, Edmond, OK 73013

by Qualgen, LLC

Reason: Lack of Assurance of Sterility
Published: November 14, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Tesamorelin, 1mg/vial, 6mL vial, Lyophilized Powder for Reconstitution and Subcutaneous Injection, Rx Only, Tailor Made Compounding, Nicholasville, KY 40356

by Tailor Made Compounding

Reason: Labeling: Incorrect or Missing Lot and/or Expiration Date; vial indicates a 1 year expiration date instead of a 6 month expiration date
Published: November 14, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Ortho-Novum 7/7/7 (norethindrone/ethinyl/estradiol) Tablets, 0.5 mg/0.035 mg, 0.75 mg/0.035 mg, 1 mg/0.035, 28-Day Regimen per pouch, packaged in a) 6 Veridate Tablet Dispensers and 6 Refill pouches (NDC 504-58-178-28) per carton (NDC 50458-178-06); and b) 12 Veridate Tablet Dispenser Refills (NDC 50458-178-12) per carton (NDC 50458-178-12), Clinic Package, , Rx Only, Manufactured by: Janssen Ortho, LLC, Manati, Puerto Rico 00674; Manufactured for: Janssen Pharmaceuticals, Inc., Titusville, New Jersey 08560.

by Janssen Pharmaceuticals, Inc.

Reason: Labeling: Incorrect Instructions; Instructions included for use with the Veridate dispenser contained instructions for the Dialpak dispenser.
Published: November 14, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Native Remedies VaricoGo Oral Spray, 2 fl oz (59 mL) per bottle, Distributed by: Silver Star Brands, Oshkosh, WI 54906. NDC 68703-105-59

by Silver Star Brands

Reason: Microbial Contamination of Non-Sterile Products
Published: November 14, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Testosterone 200 mg/Anastrozole 20 mg pellet, 1 count (NDC 69761-222-01), 6 count (NDC 69761-222-06), 12 count (NDC 69761-222-12), and 30 count (NDC 69761-222-30) vials, Rx Only, Qualgen, Edmond, OK 73013

by Qualgen, LLC

Reason: Lack of Assurance of Sterility
Published: November 14, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Testosterone 50mg pellet, 1 count (NDC 69761-150-01), 6 count (NDC 69761-150-06), 12 count (NDC 69761-150-12), and 30 count (NDC 69761-150-30) vials, Rx Only Qualgen, LLC, Edmond, OK 73013

by Qualgen, LLC

Reason: Lack of Assurance of Sterility
Published: November 14, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Testosterone 25 mg pellet, 1 count (NDC: 69761-125-01) and 30 count vials (NDC: 69761-125-30), Rx Only Qualgen, LLC, Edmond, OK 73013

by Qualgen, LLC

Reason: Lack of Assurance of Sterility
Published: November 14, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Testosterone 100mg pellet, 1 count (NDC 69761-110-01), 6 count (NDC 69761-110-06), 12 count (NDC 69761-110-12), and 30 count (NDC 69761-110-30) vials, Rx Only Qualgen, LLC, Edmond, OK 73013

by Qualgen, LLC

Reason: Lack of Assurance of Sterility
Published: November 14, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Estradiol 15mg pellet, 1 count (NDC 69761-015-01), 6 count (NDC 69761-015-06), 12 count (NDC 69761-015-12), and 30 count (NDC 69761-015-30) vials, Rx Only, Qualgen, LLC, Edmond, OK 73013

by Qualgen, LLC

Reason: Lack of Assurance of Sterility
Published: November 14, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Estradiol 12.5mg pellet, 1 count (NDC 69761-012-01), 6 count (NDC 69761-012-06), 12 count (NDC 69761-012-12), and 30 count (NDC 69761-012-30) vials, Rx Only, Qualgen, LLC, Edmond, OK 73013

by Qualgen, LLC

Reason: Lack of Assurance of Sterility
Published: November 14, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Metoprolol Tartrate Injection, USP, 5 mg/ 5 mL (1 mg/mL), 5 mL per sterile single use glass vial, Rx Only, Manufactured for: Claris Lifesciences, Inc., North Brunswick, NJ 08902. By: Claris Injectables Ltd., Gujarat, India. NDC: 36000-033-10

by Baxter Healthcare Corporation

Reason: Failed pH Specifications: Upward shift in the pH of the solution within the shelf life of the impacted lots.
Published: November 14, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Ortho-Novum 1/35 (norethindrone/ethinyl estradiol) Tablets, 1 mg/0.035 mg, 28-Day Regimen per pouch (NDC 50458-176-28), 6 Veridate Tablet Dispensers and 6 refills per carton (NDC 50458-176-06), Rx only, Manufactured by: Janssen Ortho, LLC, Manati, Puerto Rico 00674; Manufactured for: Janssen Pharmaceuticals, Inc., Titusville, New Jersey 08560.

by Janssen Pharmaceuticals, Inc.

Reason: Labeling: Incorrect Instructions; Instructions included for use with the Veridate dispenser contained instructions for the Dialpak dispenser.
Published: November 14, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

0.9% Sodium Chloride Injection, USP Rx Only a) 250 mL NDC 0409-7983-02; b) 150 mL NDC 0409-7983-61; c) 50 mL NDC 0409-7984-36; d) 100 mL NDC 0409-7984-37, Hospira, Inc. Lake Forest, IL 60045

by ICU Medical Inc

Reason: Lack of Assurance of Sterility; bags have the potential to leak
Published: November 14, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

5% Dextrose Injection, USP, Rx Only, a) 25 mL NDC 0409-7923-20; b) 250 mL NDC 0409-7922-02, Hospira, Inc. Lake Forest, IL 60045

by ICU Medical Inc

Reason: Lack of Assurance of Sterility; bags have the potential to leak
Published: November 14, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Request Foods Incorporated

Product: Gordon Choice / GFS Vegetable Egg & Cheese Frittata 60oz. U…
Reason: The firm was notified by their supplier that ingredients used in their products were possibly contaminated with Listeria monocytogenes and Salmonella.
Published: November 14, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Request Foods Incorporated

Product: Beecher's Mariachi Mac & Cheese 20oz. UPC 82045 11274 Froz…
Reason: The firm was notified by their supplier that ingredients used in their products were possibly contaminated with Listeria monocytogenes and Salmonella.
Published: November 14, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Request Foods Incorporated

Product: Love The Wild Hawaiian Style Tropical Bowl with Barramundi 9…
Reason: The firm was notified by their supplier that ingredients used in their products were possibly contaminated with Listeria monocytogenes and Salmonella.
Published: November 14, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Request Foods Incorporated

Product: Jenny Craig Butternut Squash Ravioli 213g. UPC 55447 10625…
Reason: The firm was notified by their supplier that ingredients used in their products were possibly contaminated with Listeria monocytogenes and Salmonella.
Published: November 14, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Request Foods Incorporated

Product: Moe's Southwest Vegetarian Breakfast Bowl 8oz. UPC 38000 17…
Reason: The firm was notified by their supplier that ingredients used in their products were possibly contaminated with Listeria monocytogenes and Salmonella.
Published: November 14, 2018
Distribution: Nationwide

View recall →

Data last updated: September 20, 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.