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Recall totals

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

37,142

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,799

Class I recallsReasonable probability of serious health consequences

24,349

Class II recallsTemporary or medically reversible health consequences

2,891

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/fontanini-foods-llc-recalls-raw-frozen-pork-sausage-products-due-possible-foreignPublished September 25, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 27, 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	24,349
Class I	9,799
Class III	2,891
Not Yet Classified	1

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Recalls by class
Class	Recalls
Class II	24,349
Class I	9,799
Class III	2,891
Not Yet Classified	1

FDA Recall Terminated Historical recordClass II

Fentanyl Citrate 1,500 mcg in 0.9% Sodium Chloride (10 mcg/mL) 150 mL Bag, Single-Dose Bag, Rx Only, Cantrell Drug Company 7321 Cantrell Road Little Road, AR 72207, NDC 52533-024-35

by Cantrell Drug Company

Reason: Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Published: December 21, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Calcium Chloride, (1 g/10 mL) Injection Solution 10 mL, 10% Single-Dose Vial, Rx Only, Cantrell Drug Co. 7321 Cantrell Road Little Rock, AR 72207

by Cantrell Drug Company

Reason: Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Published: December 21, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Calcium Chloride (20 mg/mL) in 0.9% Sodium Chloride 500 mL Bag, Rx Only, Single-Dose Bag Cantrell Drug Company 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-102-09

by Cantrell Drug Company

Reason: Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Published: December 21, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Phenylephrine HCl 1 mg/10 mL (100 mcg/mL) in 0.9% Sodium Chloride, 10 mL Single-Dose Syringe, Rx Only Cantrell Drug Company 7321 Cantrell Rd Little Rock, AR 72207, NDC 52533-171-12

by Cantrell Drug Company

Reason: Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Published: December 21, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Calcium Chloride 1 g/50 mL* Added to 5% Dextrose (20 mg/mL)*, Single-Dose Bag, Rx Only, Hospital/Office Use Only, Cantrell Drug Co. 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-175-37

by Cantrell Drug Company

Reason: Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Published: December 21, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

GREENCORE USA

Product: Fresh to Go Mediterranean Chicken Hummus Sandwich, Fresh Re…
Reason: Product may be contaminated with Listeria monocytogenes.
Published: December 21, 2016
Distribution: Illinois, Indiana, Iowa, Wisconsin and M…

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FDA Recall United States Terminated Historical recordClass I

Ohio Hickory Harvest Brand Products Inc.

Product: Big Y cranberry nut trail mix in plastic tub NET WT 20 OZ (1…
Reason: The firm was notified by their supplier that the products may be contaminated with Listeria monocytogenes..
Published: December 21, 2016
Distribution: Product was shipped to the following sta…

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FDA Recall United States Terminated Historical recordClass I

Ohio Hickory Harvest Brand Products Inc.

Product: Club Chef Raisin Sunflower Mix 4.8 oz bag
Reason: The firm was notified by their supplier that the products may be contaminated with Listeria monocytogenes..
Published: December 21, 2016
Distribution: Product was shipped to the following sta…

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FDA Recall United States Terminated Historical recordClass I

Ohio Hickory Harvest Brand Products Inc.

Product: Hickory Harvest FOODS Sweet & Salty Trail Mix 25 lb. UPC 0-3…
Reason: The firm was notified by their supplier that the products may be contaminated with Listeria monocytogenes..
Published: December 21, 2016
Distribution: Product was shipped to the following sta…

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FDA Recall United States Terminated Historical recordClass I

Ohio Hickory Harvest Brand Products Inc.

Product: Roasted No Salt Sunflower Kernel s under the following brand…
Reason: The firm was notified by their supplier that the products may be contaminated with Listeria monocytogenes..
Published: December 21, 2016
Distribution: Product was shipped to the following sta…

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FDA Recall United States Terminated Historical recordClass I

Ohio Hickory Harvest Brand Products Inc.

Product: Roasted & Salted Sunflower Kernels under the following brand…
Reason: The firm was notified by their supplier that the products may be contaminated with Listeria monocytogenes.
Published: December 21, 2016
Distribution: Product was shipped to the following sta…

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FDA Recall United States Terminated Historical recordClass I

Ohio Hickory Harvest Brand Products Inc.

Product: Hickory Harvest FOODS Rucker's Cajun Mix 25 lb. bag in a box…
Reason: The firm was notified by their supplier that the products may be contaminated with Listeria monocytogenes..
Published: December 21, 2016
Distribution: Product was shipped to the following sta…

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FDA Recall Terminated Historical recordClass II

USCG Boat Response Kit - Product Code 80-0353, North American Rescue

by North American Rescue LLC.

Reason: Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
Published: December 14, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Aid Backpack Kit - Product Code 85-0917, North American Rescue

by North American Rescue LLC.

Reason: Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
Published: December 14, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Mini Resupply Trauma Kit - Product Code 85-0835, North American Rescue

by North American Rescue LLC.

Reason: Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
Published: December 14, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Amphibious Trauma Kit - Product Code 85-0639, North American Rescue

by North American Rescue LLC.

Reason: Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
Published: December 14, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

K-9 Trauma Field Kit - Product Code 80-0211, 80-0304, 80-0209, 80-0210, 80-0300, 80-0301, North American Rescue

by North American Rescue LLC.

Reason: Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
Published: December 14, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Advance Trauma Kit - Product Code 85-0742, 85-0746, 85-0745, 85-0639, 85-0744, 85-0744, 85-0741, North American Rescue

by North American Rescue LLC.

Reason: Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
Published: December 14, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Range Trauma Kit - Product Code 85-1274, North American Rescue

by North American Rescue LLC.

Reason: Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
Published: December 14, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Range Trauma Kit ORG - Product Code 80-0213, 80-0299, 80-0298, North American Rescue

by North American Rescue LLC.

Reason: Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
Published: December 14, 2016
Distribution: Nationwide

View recall →

Data last updated: September 27, 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.