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Recall totals

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

37,449

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,872

Class I recallsReasonable probability of serious health consequences

24,509

Class II recallsTemporary or medically reversible health consequences

2,932

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 2,096 recalls

Newest recallhttps://www.fsis.usda.gov/recalls-alerts/fsis-issues-public-health-alert-meat-and-poultry-products-due-misbranding-andPublished November 6, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated November 8, 2026 ET

Summary (Year to date)

1,956 recalls have been announced year to date.
Oct 2026 was 4% higher than the previous complete period (Sep 2026: 209).
The highest complete period was Jun 2026 (300).
Nov 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,509
Class I	9,872
Class III	2,932
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,509
Class I	9,872
Class III	2,932
Not Yet Classified	2

FDA Recall United States TerminatedTerminated: November 16, 2018Historical recordClass I

Wegmans Food Markets, Inc.

Product: Wegmans Pumpkin Loaf, 19 oz., UPC 77890 27002
Reason: Product contains undeclared milk.
Published: November 21, 2018
Distribution: Wegmans stores located in New York, New…

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FDA Recall TerminatedTerminated: August 25, 2019Historical recordClass II

Healthful Naturals Leg Cramp Support Oral Spray, 2 fl oz (59 mL) per bottle, Distributed by: Silver Star Brands, Oshkosh, WI 54906 NDC 68703-206-02

by Silver Star Brands

Reason: CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.
Published: November 14, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: August 25, 2019Historical recordClass II

Healthful Naturals DizziFree Oral Spray, 2 fl oz (59 mL) per bottle, Distributed by: Silver Star Brands, Oshkosh, WI 54906. NDC 68703-204-02

by Silver Star Brands

Reason: CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.
Published: November 14, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: August 25, 2019Historical recordClass I

Native Remedies EyeClear Pro Oral Spray, 2 fl oz (59 mL) per bottle, Distributed by: Silver Star Brands, Oshkosh, WI 54906. NDC 68703-151-59

by Silver Star Brands

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

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FDA Recall TerminatedTerminated: August 25, 2019Historical recordClass I

Native Remedies HypoSlim Oral Spray, 2 fl oz (59 mL) per bottle, Distributed by: Silver Star Brands, Oshkosh, WI 54906. NDC 68703-275-02

by Silver Star Brands

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

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FDA Recall TerminatedTerminated: August 25, 2019Historical recordClass I

Native Remedies VertiFree Oral Spray, 2 fl oz (59 mL) per bottle, Distributed by: Silver Star Brands, Oshkosh, WI 54906. NDC 68703-253-02

by Silver Star Brands

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

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FDA Recall TerminatedTerminated: September 4, 2020Historical recordClass II

SparkleFresh Fluoride Toothpaste, Sodium Monofluorophosphate 0.76%, a) 17 g tube (NDC 53329-083-92, product number NONTP6I), b) 24 g tube (NDC 53329-083-93, product number NONTP85I), c) 42.5 g (NDC 53329-083-21, product number NONTP15I), d) 24 g tube (NDC 53329-081-93, product number DGN1000), Made in Malaysia for Medline Industries, Inc., Three Lakes Drive, Northfield, IL 60093 USA

by Medline Industries Inc

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

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FDA Recall TerminatedTerminated: June 4, 2020Historical recordClass II

Testosterone 87.5mg pellet, 1 count (NDC 69761-187-01), 6 count (NDC 69761-187-06), 12 count (NDC 69761-187-12), and 30 count (NDC 69761-187-30) 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 TerminatedTerminated: June 4, 2020Historical recordClass II

Testosterone 37.5 mg pellet, 1 count (NDC 69761-137-01), 6 count (NDC 69761-137-06), 12 count (NDC 69761-137-12) and 30 count (NDC 69761-137-30) 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 TerminatedTerminated: June 4, 2020Historical recordClass II

Testosterone 200mg pellet, 1 count (NDC 69761-120-01), 6 count (NDC 69761-120-06), 12 count (NDC 69761-120-12), and 30 count (NDC 69761-120-30) 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 TerminatedTerminated: June 4, 2020Historical recordClass II

Testosterone 12.5mg pellet, 1 count (NDC 69761-112-01), 6 count (NDC 69761-112-06), 12 count (NDC 69761-112-12), and 30 count (NDC 69761-112-30) 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 TerminatedTerminated: June 4, 2020Historical recordClass II

Estradiol 6 mg pellet, 1 count (NDC 69761-006-01), 6 count (NDC 69761-006-06), 12 count (NDC 69761-006-12), and 30 count (NDC 69761-006-30) 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 TerminatedTerminated: June 4, 2020Historical recordClass II

Estradiol 25mg pellet, 1 count (NDC 69761-025-01), 6 count (NDC 69761-025-06), 12 count (NDC 69761-025-12), and 30 count (NDC 69761-025-30) 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 TerminatedTerminated: June 4, 2020Historical 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 TerminatedTerminated: June 4, 2020Historical 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 TerminatedTerminated: August 21, 2019Historical 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 TerminatedTerminated: October 30, 2019Historical 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 TerminatedTerminated: August 25, 2019Historical 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 TerminatedTerminated: June 4, 2020Historical 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 TerminatedTerminated: June 4, 2020Historical 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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Data last updated: November 8, 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.