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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 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

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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 TerminatedTerminated: May 1, 2019Historical recordClass II

Ephedrine sulfate 5 mg/mL in 0.9% Sodium Chloride 10 mL in Single Dose Syringe, Total Volume 10 mL, Rx only, SCA Pharmaceuticals, 8821 Knoedl Ct. Little Rock, AR 72205, NDC 70004-0600-12

by SCA Pharmaceuticals

Reason: Labeling: Incorrect or Missing Lot and/or Exp Date - product label was missing lot number and beyond use date.
Published: January 17, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 20, 2019Historical recordClass II

Viokace (pancrelipase) tablets, 20,880 USP units, 100-count bottle, Rx only, Distributed by; Allergan USA Inc., Irvine, CA 92612, Manufactured in Canada, NDC 58914-117-10

by ALLERGAN

Reason: Subpotent Drug: One lot of Viokace is being recalled since product stability testing results did not meet the specifications for enzyme profile.
Published: January 17, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: October 11, 2019Historical recordClass III

Enoxaparin Sodium, Injection 120 mg/0.8 mL, pre-filled, packaged in 10-count cartons, Rx Only, Winthrop US., a business of Sanofi-aventis, U.S. LLC Bridgewater, NJ 08807, NDC 0955-1012-10

by Sanofi-Aventis U.S. LLC

Reason: Labeling: Label Error on Declared Strength. A single syringe labeled as 150 mg/1.0 mL was found packaged in a blister labeled as 120 mg/mL
Published: January 17, 2018
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: August 17, 2018Historical recordClass II

Coconuthead, LLC

Product: CO YO Coconut Yogurt Alternative CHOCOLATE, 5.3 oz and 12 oz…
Reason: Coconuthead LLC is recalling CO YO Coconut Yogurt Alternative CHOCOLATE due to container bloating.
Published: January 17, 2018
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: April 26, 2018Historical recordClass II

Nutricia North America

Product: SHS Wel-Plan Wheat and Corn Strach Baking Mix , 400 g box,Ca…
Reason: Nutricia North America, Inc. has decided to recall SHS Wel-Plan Baking Mix , 400 g box because testing of the product has detected a low level (0.74 cfu/g) contamination of Klebsiella pneumonia. The product is a baking mix and is intended to be cooked, which would kill K. pneumonia. The recall is being conducted out of an abundance of caution to avoid the risk that some consumers may misuse the product and consume it without cooking.
Published: January 17, 2018
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: June 19, 2018Historical recordClass II

American Sugar Refining, Inc.

Product: Sugar Syrup / Bulk / Tanker Truck #1 & 2
Reason: Firm was notified on 12/13/2017 by a customer that their company had found metal on their off loading strainer. The metal was identified to be fine metallic powder and thin strands with 1/32" diameter / steel wool. The firm, upon confirming that the material did come from their Tank Truck #1 filled with Sugar Syrup initiated a recall. The firm has not received any notification of injury or sickness or deaths from consumption by any customers finished goods made with our products.
Published: January 17, 2018
Distribution: This product was distributed within the…

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FDA Recall United States TerminatedTerminated: February 15, 2018Historical recordClass I

Nodine's Smokehouse Inc.

Product: Smoked salmon in 1.5 oz. and 8 oz. packages
Reason: Product may be contaminated with Listeria monocytogenes.
Published: January 17, 2018
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: March 27, 2018Historical recordClass II

Harrisburg Dairies, Inc

Product: 365 brand Egg Nog, Grade A; 1 qt. and 1/2 GAL; and Harris…
Reason: Dried Egg Yolks was not specifically stated in ingredient statement
Published: January 17, 2018
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: May 31, 2018Historical recordClass II

Saputo Cheese USA Inc.

Product: Light String Cheese, Part Skim Mozzarella cheese, sold under…
Reason: cheese has an off odor / off taste.
Published: January 17, 2018
Distribution: Multiple states

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FDA Recall TerminatedTerminated: October 5, 2020Historical recordClass I

Midazolam Injection, USP, Preservative Free, 2 mg / 2 mL (1 mg / mL), 24 X 2mL Prefilled single-use syringes per carton, Rx only, Fresenius Kabi Lake Zurich, IL 60047, NDC 76045-001-20

by Fresenius Kabi USA, LLC

Reason: Labeling: Label MIX-UP. Blister Packages, Labeled as Midazolam injection, USP, 2 mg / 2 ml, Containing Syringes of Ondansetron Injection, USP, 4 mg / 2 mL
Published: January 10, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 2, 2020Historical recordClass II

Zoloft (sertraline HCl) tablets 25 mg* 30-count bottle, Rx only, Distributed by Roerig Division of Pfizer Inc., NY, NY, 10017 NDC 0049-4960-30

by Pfizer Inc.

Reason: SUPERPOTENT: Weight variations resulting in tablets that are sub and super potent
Published: January 10, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 2, 2020Historical recordClass I