Category Archives: FDA

USA – Twin City Foods, Inc., Recalls Frozen Super Sweet Corn and Mixed Vegetables Because of Possible Health Risk – Listeria monocytogenes

FDA

Summary

Company Announcement Date:
FDA Publish Date:
Product Type:
Food & Beverages
Reason for Announcement:
Potential Foodborne Illness
Company Name:
Twin City Foods, Inc.
Brand Name:
Food Lion, Kroger and more
Product Description:
Frozen sweet corn and mixed vegetables

Company Announcement

August 22, 2023, Twin City Foods, Inc. of Stanwood, Washington, is voluntarily recalling a limited quantity of Not-Ready-To Eat Individually Quick Frozen (IQF) Super Sweet Cut Corn and Mixed Vegetables in retail bags, due to a potential for these products to be contaminated with Listeria monocytogenesListeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, listeria infection can cause miscarriages and stillbirths among pregnant women.

The following products were distributed nationwide by the following retailers. No other products have been affected.

Product Name UPC Lot and Best if Used By Date
FOOD LION Mixed Vegetables Carrots, Corn, Green
Beans & Peas, net wt. 16oz
35826005090 50183 BEST BY 18 JAN 2025 PROD OF USA
FOOD LION Super Sweet Cut Yellow Corn, net wt. 16oz. 35826079855 53072 BEST BY 03 NOV 2024 PROD OF USA
FOOD LION Super Sweet Cut Yellow Corn, net wt. 16oz. 35826079855 53622 BEST BY 28 DEC 2024 PROD OF USA
Kroger Mixed Vegetables Carrots, Super Sweet Corn,
Green Beans & Green Peas, net wt. 32 oz
11110865854 BEST IF USED BY FEB.2024 82352 SIDE ID,TIME
Kroger Mixed Vegetables Carrots, Super Sweet Corn,
Green Beans & Green Peas, net wt. 12 oz.
11110849625 53122 BEST IF USED BY MAY 2024 PROD OF USA
Kroger Mixed Vegetables Carrots, Super Sweet Corn,
Green Beans & Green Peas, net wt. 12 oz.
11110849625 53412 BEST IF USED BY JUN 2024 PROD OF USA
Kroger Mixed Vegetables Carrots, Super Sweet Corn,
Green Beans & Green Peas, net wt. 12 oz.
11110849625 53412 BEST IF USED BY JUN 2024 PROD OF USA
Kroger Mixed Vegetables Carrots, Super Sweet Corn,
Green Beans & Green Peas, net wt. 12 oz.
11110849625 BEST IF USED BY APR.2024 82942 SIDE ID, TIME
Kroger Mixed Vegetables Carrots, Super Sweet Corn,
Green Beans & Green Peas, net wt. 12 oz.
11110849625 BEST IF USED BY APR.2024 83012 SIDE ID, TIME
Kroger Super Sweet Corn, net wt. 32 oz. 11110865786 53052 BEST IF USED BY MAY 2024 PROD OF USA
Kroger Super Sweet Corn, net wt. 32 oz. 11110865786 53112 BEST BY MAY 2024 PROD OF USA
Kroger Super Sweet Corn, net wt. 32 oz. 11110865786 BEST IF USED BY APR.2024 82932 SIDE ID, TIME
Kroger Super Sweet Corn, net wt. 32 oz. 11110865786 BEST IF USED BY APR.2024 83012 SIDE ID, TIME
Kroger Super Sweet Corn, net wt. 12 oz. 11110849618 52842 BEST IF USED BY APR 2024 PROD OF USA
Kroger Super Sweet Corn, net wt. 12 oz. 11110849618 53042 BEST IF USED BY APR 2024 PROD OF USA
Kroger Super Sweet Corn, net wt. 12 oz. 11110849618 53272 BEST IF USED BY MAY 2024 PROD OF USA
Kroger Super Sweet Corn, net wt. 12 oz. 11110849618 53542 BEST IF USED BY JUN 2024 PROD OF USA
Kroger Super Sweet Corn, net wt. 12 oz. 11110849618 50043 BEST IF USED BY JUL 2024 PROD OF USA
Kroger Super Sweet Corn, net wt. 12 oz. 11110849618 50033 BEST IF USED BY JUL 2024 PROD OF USA
Kroger Super Sweet Corn, net wt. 12 oz. 11110849618 BEST IF USED BY FEB.2024 82352 SIDE ID,TIME
Kroger Super Sweet Corn, net wt. 12 oz. 11110849618 BEST IF USED BY APR.2024 82842 SIDE ID, TIME
Signature Select Golden Corn Super Sweet, net wt. 12oz 21130090655 BEST IF USED BY FEB.22.24 S5716 TIME,SIDE ID

To date, there have been no actual consumer reports of human illness or other complaints associated with this product.

The recall has been initiated because finished products may potentially be contaminated with the Listeria monocytogenes, based on one customer’s 3rd party lab results for the IQF sweet cut corn.

Consumers who have purchased the affected product are urged not to consume the product and immediately return the product to the store where they purchased it for a full refund.

This recall is being made with the knowledge of the Food and Drug Administration.

Consumers with any questions may contact Twin City Foods at (360) 629-5678 Monday through Friday, between 8:00 a.m. and 5:00 p.m. (Eastern Time).


Company Contact Information

Consumers:
Twin City Foods
 360-629-5678

USA – Outbreak Investigation of Listeria: Ice Cream (August 2023)

FDA

Product 

  • Real Kosher Ice Cream has voluntarily recalled all flavors of Soft Serve On The Go 8-oz ice cream cups 
    • Soft Serve On The Go Vanilla Chocolate
    • Soft Serve On The Go Razzle
    • Soft Serve On The Go Caramel
    • Soft Serve On The Go Parve Vanilla Chocolate
    • Soft Serve On The Go Sorbet Strawberry Mango
    • Soft Serve On The Go Lite Peanut Butter

FDA’s investigation is ongoing. Products may be added to this advisory. Additional recall information is available below.

Stores Affected

  • Multiple retailers in CA, CO, CT, DC, DE, FL, IL, MA, MD, MI, MN, NC, NH, NJ, NY, OH, OR, PA, VA, WV.

Symptoms of Listeriosis (Listeria Infection)

Illness can occur within a few hours or as long as two to three days after eating contaminated food. More severe forms of listeriosis may take anywhere from three days to three months to develop. Mild symptoms may include a fever, muscle aches, nausea, vomiting, and diarrhea. If the more severe form of listeriosis develops, symptoms may include headache, stiff neck, confusion, loss of balance, and convulsions.

Status

Ongoing

Recommendation

  • Consumers, restaurants, and retailers should not eat, sell, or serve recalled Soft Serve On The Go ice cream and should throw the recalled product away or return it to the place of purchase for a full refund. This recall includes all flavors of Soft Serve On The Go 8-oz cups.
  • Ice cream has a long shelf life and may still be in freezers. Consumers, restaurants, and retailers should check their freezers and throw away recalled ice cream products or return it to the place of purchase for a full refund.
  • Consumers, restaurants, and retailers who purchased or received any recalled ice cream products should follow FDA’s safe handling and cleaning advice and use extra vigilance in cleaning and sanitizing any surfaces and containers that may have come in contact with these products to reduce the risk of cross-contamination. Listeria can survive temperatures at or below freezing and can easily spread to other foods and surfaces.

Recommendation for At-Risk Groups:

  • Listeria is most likely to sicken pregnant people and newborns, adults aged 65 or older, and people with weakened immune systems. Other people can be infected with Listeria, but they rarely become seriously ill.
  • Pregnant people typically experience only fever, fatigue, and muscle aches. However, Listeria infection during pregnancy can lead to miscarriage, stillbirth, premature delivery, or life-threatening infection of the newborn.
  • Call your healthcare provider right away if you have symptoms of a Listeria infection.

Current Update

August 22, 2023

The U.S. Food and Drug Administration (FDA) and Centers for Disease Control and Prevention (CDC), in collaboration with state and local partners, are investigating an outbreak of Listeria monocytogenes infections linked to Soft Serve On The Go cups produced by Real Kosher Ice Cream of Brooklyn, NY.

The Pennsylvania Department of Agriculture collected an unopened sample of Soft Serve On The Go from an ill person’s home. This sample was reported as positive for Listeria monocytogenes. Whole Genome Sequencing (WGS) analysis confirmed that the strain of Listeria found in the sample from the patient’s home matches the strain of Listeria causing illnesses in this outbreak.

Additionally, product sampling was conducted by the New York State Department of Agriculture and Markets at Real Kosher Ice Cream’s manufacturing location. Five finished product samples of Soft Serve On The Go Vanilla Chocolate ice cream were reported as positive for Listeria monocytogenes. WGS analysis confirmed that the strain of Listeria found in these products matches the outbreak strain.

FDA’s investigation is ongoing. Updates to this advisory will be provided as they become available.

USA – FDA issues advisory over Darwin’s Natural Pet Products over Salmonella concerns

Food Safety News

The U.S. Food and Drug Administration (FDA) has issued a cautionary advisory to consumers, urging them not to feed their pets specific lots of raw cat food and dog food produced by Arrow Reliance Inc.’s brand, Darwin’s Natural Pet Products. The agency’s move comes after samples from the affected lots tested positive for Salmonella contamination.

The FDA’s advisory was spurred by the potentially severe health implications these contaminated pet food lots can cause for both animals and humans. Salmonella infections can lead to serious illness, especially in individuals with weakened immune systems, the elderly, and young children. Since the affected products are typically stored frozen, the FDA is particularly worried that people might still have them and unwittingly feed them to their pets.

The FDA identified the potentially hazardous products as follows:

  • Darwin’s Natural Pet Products Natural Selections Chicken Recipe with Organic Vegetables for Dogs, Lot 9774, manufactured on June 13, 2023.
  • Darwin’s Natural Pet Products Natural Selections Chicken Recipe for Cats, Lot 9795, manufactured on June 28, 2023.
  • Darwin’s Natural Pet Products Natural Selections Chicken Recipe for Cats, Lot 9830, manufactured on July 19, 2023.

USA – FDA – Core Investigation Table

FDA

What’s New

  • A new outbreak of Listeria monocytogenes (ref #1172) in a not yet identified product has been added to the table. There are two cases in this outbreak. FDA has initiated traceback.
  • For the outbreak of Cyclospora cayetanensis (ref #1171), the case count has increased from 47 to 55 cases.
  • For the outbreak of E. coli O157:H7 (ref #1166), the outbreak has ended and FDA’s investigation has closed.
  • For the outbreak of Salmonella Paratyphi B var. L(+) tartrate+ (ref #1157), the case count has increased from 36 to 37 cases.

USA – Real Kosher Ice Cream Recalls Soft Serve on the Go Cups Because of Possible Health Risk – Listeria monocytogenes

FDA

Summary

Company Announcement Date:
FDA Publish Date:
Product Type:
Food & Beverages
Foodborne Illness
Reason for Announcement:
Possible Listeria monocytogenes contamination
Company Name:
Real Kosher Ice Cream
Brand Name:
Soft serve on the go
Product Description:
Soft serve ice cream and sorbet cups

Company Announcement

Real Kosher Ice Cream of Brooklyn, NY is recalling soft serve on the go ice cream and sorbet cups, because it has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.

SOFT SERVE ON THE GO CUPS were distributed in the states of CA, CO, CT, DC, DE, FL, IL, MA, MD, MI, MN, NC, NH, NJ, NY, OH, OR, PA, VA, WV.

The recalled product reached consumers through Canteens, Grocery and Convenience stores etc.

The recalled product is packaged in an 8 fl oz., clear plastic cup. The product looks like a soft serve cup served in an ice cream store, with a clear plastic cover with a seal and spoon attached to it.

The product brand name is Soft Serve On The Go cups, All flavors, UPC (SEE LIST)

Soft Serve on the go Vanilla Chocolate, 8 fl oz UPC 0-91404-15129-0
Soft Serve on the go Razzle, 8 fl oz UPC 0-91404-15133-7
Soft Serve on the go Caramel, 8 fl oz UPC 0-91404-15131-3
Soft Serve on the go Parve Vanilla Chocolate, 8 fl oz UPC 0-91404-15113-9
Soft Serve on the go Sorbet Strawberry Mango, 8 fl oz UPC0-91404-15128-3
Soft Serve Lite Peanut Butter, 8 fl oz UPC0-91404-15285-3

The UPC is the only identifiable code on the package. It does not have any LOT number or best by date. All product produced up to 8/4/23 is being recalled.

To date, two cases of illness have been reported in this outbreak in two states (NY and PA). Both individuals were hospitalized but no deaths have been reported to date.

The recall is the result of an individual becoming ill and reporting to have eaten this product. Pennsylvania Department of Agriculture tested samples of product and one sample tested positive for Listeria monocytogenes.

The company has ceased the production and distribution of the product as FDA and the company continue their investigation as to what caused the problem.

Consumers should discontinue consumption of the product immediately. Please dispose of this product or return to your store of purchase for full credit. Consumers with questions may contact our Soft Serve on the Go team at: 845-668-4346 or info@softserveonthego.com . Monday thru Friday 9am to 5 pm EST.

USA- David Oppenheimer and Company I, LLC Voluntarily Recalls Organic Green Kiwifruit Due to Possible Health Risk – Listeria monocytogenes

FDA

Zespri organic green kiwifruit, one-pound clear plastic clamshells

David Oppenheimer and Company I LLC is voluntarily recalling from the market all one-pound clamshells of organic green kiwifruit described below because they have the potential to be contaminated with Listeria monocytogenesListeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.  Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, listeria infection can cause miscarriages and stillbirths among pregnant women.

The recalled organic green kiwifruit is grown in New Zealand, exported to North America and repacked locally for sale in one-pound clear plastic clamshells bearing the Zespri brand and UPC code 8 18849 02009 3, containing fruit stickered with the GTIN bar code 9400 9552.

The organic green kiwifruit subject to the voluntary recall was shipped between June 14, 2023 and July 7, 2023, and sold in clamshells at retail locations in FL, GA, IL, IN, KY, MI, NC, NY, OH, PA, TN, TX, VA, and WI.  Zespri organic green kiwifruit sold in other states is NOT subject to this recall.

Zespri organic green kiwifruit shipped after August 7, 2023 in one-pound plastic clamshells with a WHITE STICKER that includes Work Order (WO) number and Packed on date is NOT affected by this recall. See example of white sticker below:

The recall was the result of a routine sampling by the Kentucky Department for Public Health on July 7, 2023. Since being notified on August 3, David Oppenheimer and Company I LLC has worked with Zespri to trace the product through the supply chain to two grower lots, and immediately ceased the distribution of organic green kiwifruit from the related grower lots as it continues its investigation in cooperation with the U.S. Food and Drug Administration. 

No illnesses have been reported to date. No other David Oppenheimer and Company I, LLC products are part of this voluntary recall.

Consumers who still have any of these products are urged not to consume the product and to discard it immediately. Consumers with questions may contact David Oppenheimer and Company I, LLC (Oppy) at 1-866-698-2580, Monday-Friday, 9am-4:30pm PDT, or send an email to contact@oppy.com.

USA – FDA – Investigations of Foodborne Illness Outbreaks

FDA

What’s New

  • For the outbreak of Cyclospora cayetanensis (ref #1171), the case count has increased from 39 to 47 cases.
  • For the outbreak of Cyclospora cayetanensis (ref #1163), the case count has increased from 121 to 140 cases.
  • For the outbreak of Salmonella Paratyphi B var. L(+) tartrate+ (ref #1157), the case count has increased from 35 to 36 cases.
  • For the outbreak of Cyclospora cayetanensis (ref #1159), the case count has increased from 68 to 69 cases.

USA – FDA – Investigations of Foodborne Illness Outbreaks

FDA

What’s New

  • For the outbreak of E. coli O157:H7 (ref #1166), the case count has increased from 11 to 12.
  • For the outbreak of Cyclospora cayetanensis (ref #1163), the case count has increased from 112 to 118 cases.
  • For the outbreak of Cyclospora cayetanensis (ref #1159), the case count has increased from 38 to 43 cases. This incident now includes additional illnesses based on similarities in reported exposures.
  • For the outbreak of Salmonella Enteritidis (ref #1156) linked to raw cookie dough, the advisory was updated on July 13, 2023. The outbreak has ended and FDA’s investigation is closed.
  • For the investigation linked to Morel mushrooms (ref #1152), the advisory was updated on July 19, 2023. The outbreak has ended, and FDA’s investigation is closed.

USA – How the FDA Uses Traceback to Respond to Foodborne Illness Outbreaks

FDA

Every year the FDA responds to dozens of foodborne outbreaks, but what does that mean? What are the steps the FDA and other public health agencies take to determine the source of a foodborne illness outbreak and protect public health?

In a video and infographic, the FDA provides an overview of the traceback process used to examine the complex path of food as it travels through the supply chain. Typically, in a traceback investigation, investigators trace food that ill people report eating all the way back to a farm or production facility. Finding commonalities in the supply chains of foods eaten by ill people helps investigators zero in on a potential source of the outbreak. Traceback is one tool used by FDA investigators during the many steps taken by the agency along with the Centers for Disease Control and Prevention (CDC) and local, state, and international public health authorities to respond to outbreaks in FDA-regulated food products.

The video explores how the CDC works with public health authorities to learn more about what might be making consumers sick, and then if an FDA-regulated food product is identified, how the FDA investigates the cause of the outbreak and works with industry to remove any potentially contaminated product from store shelves. The FDA, CDC, and local and state partners also work together to warn the public, as appropriate, and to help prevent additional illnesses.

Infographic (PDF)

USA – FDA Advises Restaurants, Retailers and Consumers to Avoid Certain Fortune Brand Raw Oysters from Nova Scotia Contaminated with Norovirus

FDA

Audience

Restaurants and food retailers that have received shipments of oysters harvested from NS 10, an oyster harvest area in Nova Scotia, Canada on June 9, 2023, and were distributed by Bill and Stanley Oyster Co. of Nova Scotia, Canada through U.S. distributors to 17 states and the District of Columbia: CA, CO, CT, DC, DE, FL, GA, IN, MA, MD, MI, MN, NJ, NY, OH, PA, TX, and WI. The FDA is working to obtain additional information on distribution of the oysters and will continue to monitor the investigation, provide assistance to state authorities, and update our communications to the public as needed.

Consumers, especially those who are or could become pregnant, the elderly, and persons with weakened immune systems, who have recently consumed raw oysters and suspect they have food poisoning should seek medical care immediately.

Product

  • Fortune brand oysters harvested from harvest location NS 10 in Nova Scotia, Canada on June 9, 2023 that were distributed to 17 states and the District of Columbia: CA, CO, CT, DC, DE, FL, GA, IN, MA, MD, MI, MN, NJ, NY, OH, PA, TX, and WI.
  • Oyster containers include the harvest area information and original shipper certification number NS 6024 SS WS on the attached product tag.

Purpose

The US Food and Drug Administration (FDA) is advising consumers not to eat, and restaurants and food retailers not to sell, and to dispose of raw oysters that were harvested from harvest location NS 10 in Nova Scotia, Canada on June 9, 2023 and were distributed to 17 states and the District of Columbia: CA, CO, CT, DC, DE, FL, GA, IN, MA, MD, MI, MN, NJ, NY, OH, PA, TX, and WI. Consumers who purchased oysters after June 9, 2023 should check the packaging to see if they were harvested from location NS 10 on June 9, 2023. Contaminated shellfish can cause illness if eaten raw, particularly in people with compromised immune systems. Food contaminated with norovirus may look, smell, and taste normal. Consumers of these products who are experiencing symptoms of norovirus illness should contact their healthcare provider, who should report their symptoms to their local Health Department.

Summary of Problem and Scope

On June 30, 2023, the Minnesota Department of Health (MDH) reported to CDC an outbreak consisting of 9 cases of norovirus illness associated with the consumption of oysters from Nova Scotia. The oysters harvested from Nova Scotia were sold in both Canada and the U.S. FDA is working with federal, state, and local officials, and with Canadian public health authorities to investigate this outbreak, obtain additional information on distribution of the oysters, and determine if additional illnesses have occurred.

Retailers should not sell or serve raw oysters from harvest location NS 10 with a harvest date of June 9, 2023, which will be printed on product tags.

Shellfish can cause illness if contaminated and eaten raw, particularly in people with compromised immune systems. Food contaminated with norovirus may look, smell, and taste normal.

FDA Actions

The FDA is issuing this alert advising consumers not to eat, and restaurants and food retailers not to sell or serve, raw oysters from harvest location NS 10 on June 9, 2023 that were distributed to 17 states and the District of Columbia: CA, CO, CT, DC, DE, FL, GA, IN, MA, MD, MI, MN, NJ, NY, OH, PA, TX, and WI.

The FDA will continue to monitor the investigation and provide updates and assistance to state authorities as needed.