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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

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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated November 9, 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

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

FDA Recall TerminatedTerminated: August 28, 2023Historical recordClass II

Medline CNTRL Line Removal Kit Scripps. Packaged in USA for Medline Industries, Inc., Northfield, IL 60093

by Medline Industries Inc

Reason: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Published: February 7, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: August 28, 2023Historical recordClass II

Medline Pediatric IV Kit. Packaged in USA for Medline Industries, Inc., Northfield, IL 60093

by Medline Industries Inc

Reason: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Published: February 7, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: August 28, 2023Historical recordClass II

Medline Concordia Nurse Bag Kit. Packaged in USA for Medline Industries, Inc., Northfield, IL 60093

by Medline Industries Inc

Reason: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Published: February 7, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: August 28, 2023Historical recordClass II

Medline Concordia Trunk Kit. Packaged for Medline Industries, Inc., Northfield, IL 60093

by Medline Industries Inc

Reason: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Published: February 7, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: August 28, 2023Historical recordClass II

Medline Newborn Kit. Packaged for Medline Industries, Inc., Northfield, IL 60093

by Medline Industries Inc

Reason: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Published: February 7, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: August 28, 2023Historical recordClass II

Medline RAD NECK ENT TRAY Pack, Single Use Only. Packaged in USA for Medline Industries, Inc., Northfield, IL 60093

by Medline Industries Inc

Reason: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Published: February 7, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: August 28, 2023Historical recordClass II

Medline Vitrectomy CDS Pack, Single Use Only. Packaged in Mexico for Medline Industries, Inc., Northfield, IL 60093

by Medline Industries Inc

Reason: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Published: February 7, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: August 28, 2023Historical recordClass II

Medline Vaginal Delivery CDS Pack, Single Use Only. Packaged in Mexico for Medline Industries, Inc., Northfield, IL 60093

by Medline Industries Inc

Reason: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Published: February 7, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: August 28, 2023Historical recordClass II

Medline CC Drawer 4 IV Circulation Pack, Contains Rx, Single Use Only, contains 2 Prep Pad PVPs. Packaged in USA for Medline Industries, Inc., Northfield, IL 60093

by Medline Industries Inc

Reason: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Published: February 7, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: August 28, 2023Historical recordClass II

Aplicare Povidone-Iodine Prep Pad, Antiseptic, Sterile Solution, Active Ingredient: Povidone-iodine USP 10%. Aplicare, INC., Meriden, CT 06450 USA. NDC: 52380-0111-1

by Medline Industries Inc

Reason: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Published: February 7, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 4, 2020Historical recordClass II

Mitomycin 40 mg/mL Preservative Free Irrigation Volume: 10 mL SDV , Compounded by: Premier Pharmacy Labs 8265 Commercial Way, Weeki Wachee, FL 34613, NDC: 69623-160-35.

by Premier Pharmacy Labs Inc

Reason: Labeling: Label Error on Declared Strength
Published: February 7, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: September 21, 2020Historical recordClass III

Clobetasol Propionate Cream USP, 0.05% 60 g tube, Rx only Mfd. by: Taro Pharmaceutical Industries Ltd., Haifa Bay, Israel 2624761 Dist. by : Taro Pharmaceuticals U.S.A., Inc., Hawthorne, NY 10532 UPC 351672125837 NDC 51672-1258-3

by Taro Pharmaceuticals U.S.A., Inc.

Reason: Failed Content Uniformity Specifications
Published: February 7, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: April 23, 2018Historical recordClass III

Oxycodone Hydrochloride Tablets, USP 15 mg, 100 count bottles, Rx only, Manufactured for Camber Pharmaceuticals, Inc., Piscataway, NJ, Manufactured by: Ascent Pharmaceuticals, Inc., Central Islip, NY --- NDC 31722-917-01

by Ascent Pharmaceuticals, Inc.

Reason: Labeling; Label Error Not Elsewhere Classified; label missing controlled substance CII symbol
Published: February 7, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: December 6, 2018Historical recordClass I

BLUE PEARL capsules, 500mg, 1-count packets, Distributed by Blue Pearl Long Beach, CA UPC 8 4704600978 5

by Blue Fusion Natural

Reason: Marketed Without An Approved NDA/ANDA: FDA analysis found this product to contain undeclared sildenafil, an FDA approved drug for the treatment of erectile dysfunction, making this an unapproved drug for which safety and efficacy have not been established and therefore, subject to recall.
Published: February 7, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: August 3, 2020Historical recordClass III

Cefuroxime, Ophthalmic Solution for Injection, 10 mg/mL, 0.3 mL single-use syringe. This is a Compounded Drug, Hospital & Office Use Only, Not for Resale. Fagron Sterile Services/JCB Laboratories, 7335 W. 33rd St. N., Wichita, KS 67205

by JCB Laboratories LLC

Reason: Subpotent Drug: The product is sub-potent prior to its 90-day beyond use date.
Published: February 7, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: September 9, 2019Historical recordClass II

Neutrogena Elevated 4-Holiday Trays (contains Neutrogena Deep Clean Purifying Whipped Foam Cleanser) Case Code: 00070501302866

by Johnson & Johnson

Reason: Defective Container: products showed leakage (bubbles, foaming) of propellant and product from the container valve cup area.
Published: February 7, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: September 9, 2019Historical recordClass II

Neutrogena deep clean purifying whipped foam cleanser, (Salicylic Acid 0.5%), aerosolized product in a can, NET WT. 5 OZ. (141 g) Distributed By: Johnson & Johnson Consumer Inc. Skillman, NJ 08558. UPC: 0 70501 10053 0

by Johnson & Johnson

Reason: Defective Container: products showed leakage (bubbles, foaming) of propellant and product from the container valve cup area.
Published: February 7, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: September 9, 2019Historical recordClass II

Neutrogena Acne Proofing whipped foam cleanser, (Salicylic Acid 2%), aerosolized product in a can, NET WT. 5 OZ (141 g) , Distributed by Johnson & Johnson Consumer Inc. Skillman, NJ 08558, UPC 0 70501 11131 4

by Johnson & Johnson

Reason: Defective Container: products showed leakage (bubbles, foaming) of propellant and product from the container valve cup area.
Published: February 7, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: October 17, 2018Historical recordClass II

SPIRIVA HandiHaler (tiotropium bromide inhalation powder) 18 mcg/capsule (90 capsules (unit dose blisters) per box, Rx Only, Made in Germany, Distributed by: Boehringer Ingelheim (BI) Pharmaceuticals, Inc., Ridgefield, CT 06877, NDC 0597-0075-47

by Boehringer Ingelheim Pharmaceuticals, Inc.

Reason: Failed Stability Specifications
Published: February 7, 2018
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: March 15, 2019Historical recordClass I

Dollar General Corporation, Inc.

Product: Clover Valley¿ Iced Oatmeal Cookies NET WT 12 OZ (340 g) CON…
Reason: The firm received Ice Oatmeal Cookies that actually contain Coconut Macaroon Cookies. Product is being recalled due to mislabeling. Product contains both milk and tree nuts that are not listed in the ingredient statement.
Published: February 7, 2018
Distribution: Product was shipped to the following sta…

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Data last updated: November 9, 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.