Author Archives: KSW

Germany – Organic Primo Goji Berries – Salmonella

Lebensmittelwarnung

Alert type:

Groceries

Date of first publication:

01/03/2024

Product name:

Organic Primo Goji Berries

Product images:

Organic Primo Goji Berries.PNG

Consumer notice

Manufacturer (distributor):

Manufacturer: Bio Food Production and Trading GmbH Sales through branches of Müller Handels GmbH & Co. KG

Reason for warning: Salmonella
Packaging Unit: 100 g
Durability:

Best before dates/batches: 03/28/2024 C306284, 04/26/2024 B307267, 05/21/2024 A308213, 06/16/2024 A309163, 07/19/2024 A310193

Additional Information:

Further information can be found in the attached consumer notice.

Belgium – Special Oysters from lsigny of the brand “La Précieuse” n°3. – Norovirus

afsca

Product: Special Oysters from lsigny of the brand “La Précieuse” n°3.
Problem: Presence of Norovirus.
Following a prefectural order to close the production area due to the presence of norovirus.

DESIGNATION: Special d’Isigny Oysters, brand “La Précieuse” n°3 per dozen or 2 kg
BRAND: La Precious – Company “Les coquillages de la Baie d’Isigny”
SALE PERIOD: From 12 to

30/12/2023 product was distributed in CORA, and various MATCH AND SMATCH.

In consultation with the FASFC (Federal Agency for the Safety of the Food Chain), we have decided to withdraw this product from sale.

Customers who have purchased this product are asked not to consume it and to return it to the point of sale, where they will be refunded.
Norovirus can cause gastroenteritis in humans. The incubation period is 6 to 48 hours. The main symptoms are:
Vomiting, diarrhea, abdominal cramps, nausea, as well as less specific symptoms like fever, headache and general fatigue.
Any person who has consumed the product mentioned above and who presents these symptoms is invited to consult their doctor and report this consumption.

In the meantime, the products have been removed from the shelves and a ‘Customer Reminder’ poster is displayed at points of sale.
We offer our most sincere apologies to our customers for this inconvenience and assure them that the most effective measures are taken to avoid this type of incident.

Any customer wishing additional information can contact our Quality Department and contact the number 071.69.95.24 or by email at the address: ALERTES-RETRAITS@CORA.BE .

The CORA Quality Department

USA – Fratelli Beretta USA, Inc. Recalls Busseto Foods Brand Ready-to-Eat Charcuterie Meat Products Due to Possible Salmonella Contamination

FSIS USDA

WASHINGTON, Jan. 3, 2024 – Fratelli Beretta USA, Inc., a Mount Olive, N.J. establishment, is recalling approximately 11,097 pounds of Busseto Foods brand ready-to-eat charcuterie meat products that may be contaminated with Salmonella, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.

The ready-to-eat (RTE) charcuterie sampler product was produced on October 30, 2023. The following products are subject to recall [view labels]:

  • 18-oz. plastic tray packages containing “BUSSETO FOODS CHARCUTERIE SAMPLER Prosciutto, Sweet Sopressata, and Dry Coppa” with lot code L075330300 and “BEST IF USED BY APR 27 24.” The products are sold as a twin pack with two 9-oz. packages.

The products subject to recall bear establishment number “EST. 7543B” inside the USDA mark of inspection and “EST. #47967” printed with the lot and date codes. These items were shipped to Sam’s Club distribution centers in Georgia, Illinois, Indiana, Minnesota, North Carolina, Ohio, Oklahoma, and Texas.

The problem was discovered when FSIS was notified that a sample collected by the Minnesota Department of Agriculture tested positive for Salmonella.

FSIS is working with the Centers for Disease Control and Prevention (CDC) and state public health partners to investigate a multistate outbreak of Salmonella. Minnesota collected unopened ready-to-eat charcuterie sampler product as part of the investigation. The product tested positive for Salmonella. Further testing is ongoing to determine if the product sample is related to the outbreak. The investigation is ongoing.

Consumption of food contaminated with Salmonella can cause salmonellosis, one of the most common bacterial foodborne illnesses. The most common symptoms of salmonellosis are diarrhea, abdominal cramps, and fever within 6 hours to 6 days after eating the contaminated product. The illness usually lasts 4 to 7 days. Most people recover without treatment. In some persons, however, the diarrhea may be so severe that the patient needs to be hospitalized. Older adults, infants, and persons with weakened immune systems are more likely to develop a severe illness. Individuals concerned about an illness should contact their health care provider.

FSIS is concerned that some product may be in consumers’ refrigerators. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.

FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.

Media with questions regarding the recall can contact Marco Lastrico, Public Relations, Busseto Foods, at 917-634-1685 or m.lastrico@barabinousa.com. Consumers with questions regarding the recall can contact the Busseto Recall Hotline at 866-552-4916.

Consumers with food safety questions can call the toll-free USDA Meat and Poultry Hotline at 888-MPHotline (888-674-6854) or send a question via email to MPHotline@usda.gov. For consumers that need to report a problem with a meat, poultry, or egg product, the online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at https://foodcomplaint.fsis.usda.gov/eCCF/.

Product Images

USA – Expanded Recall Affected States: Blue Ridge Beef Issues Voluntary Recall of Blue Ridge Beef Kitten Grind, Blue Ridge Kitten Mix and Blue Ridge Beef Puppy Mix Due to Salmonella and Listeria Monocytogenes Contamination

FDA

A previous version of this press release was issued on 12/22/2023. This press release was updated to include all states that may have received the recalled product lot numbers.

STATESVILLE, NC – January 3, 2024 – Blue Ridge Beef is expanding their recall to include additional lot numbers. This recall includes all lot numbers and used by dates between N24 1114 to N24 1224 of their 2 lb log of Kitten Grind UPC 8 54298 00101 6; 2lb log of Kitten Mix UPC 8 54298 00143 6 and their 2lb log of Puppy Mix UPC 8 54298 00169 6 due to contamination of Salmonella and Listeria monocytogenesSalmonella and Listeria monocytogenes can affect animals eating the products and there is risk to humans from handling contaminated pet products, especially if they have not thoroughly washed their hands after having contact with the products or any surfaces exposed to these products.

Healthy people infected with Salmonella should monitor themselves for some or all of the following symptoms: nausea, vomiting, diarrhea or bloody diarrhea, abdominal cramping and fever. Rarely, Salmonella can result in more serious ailments, including arterial infections, endocarditis, arthritis, muscle pain, eye irritation, and urinary tract symptoms. Consumers exhibiting these signs after having contact with this product should contact their healthcare providers.

Pets with Salmonella and Listeria infections may be lethargic and have diarrhea or bloody diarrhea, fever, and vomiting. Some pets will have only decreased appetite, fever, and abdominal pain. Infected but otherwise healthy pets can be carriers and infect other animals or humans. If your pet has consumed the recalled product and has these symptoms, please contact your veterinarian.

On 12/15/2023 the firm was notified by the North Carolina Department of Agriculture and Consumer Services that one lot of each of the products were sampled and tested positive for Salmonella and Listeria monocytogenes. However, out of an abundance of caution the firm is recalling all lots with the used by dates between N24 1114 to N24 1224.

No illnesses have been reported to date.

The products were distributed between 11/14/2023 – 12/20/2023. These products were packaged in clear plastic and sold primarily in retail stores located in the states of: CT, FL, IA, IL, MA, MD, MI, NC, NY, OH, OR, PA, RI, TN, VA & WI. Image of the products are below.

Products affected are:

Product

Size

UPC

All Lot #/Use By Dates Between

Kitten Grind 2lbs 8 54298 00101 6 N24 1114 to N24 1224
Kitten Mix 2lbs 8 54298 00243 6 N24 1114 to N24 1224
Puppy Mix 2lbs 8 54298 00169 6 N24 1114 to N24 1224

The lot numbers and used by dates are located on the silver tabs at the end of the tubes.

Consumers who have purchased these products are urged to contact Blue Ridge Beef at blueridgebeefnc@yahoo.com for a full refund and destroy the food in a way that children, pets, and wildlife cannot access. Do not sell or donate the recalled products. Do not feed the recalled product to pets or any other animals. Wash and sanitize pet food bowls, cups, and storage containers. Always ensure you wash and sanitize your hands after handling recalled food or any utensils that come in contact with recalled food. Consumers with questions may contact Mr. Steven Lea at (704) 880-4500 Monday through Friday 8:00 am – 5:00 pm EST.

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


Company Contact Information

Consumers:
Mr. Steven Lea
 704-880-4500

UK -Reckitt recalls two infant formula powders because of the possible presence of Cronobacter sakazakii

FSA

Reckitt has taken the precautionary step of recalling Nutramigen LGG stage 1 and stage 2 Hypoallergenic Formula powders because of the possible presence of Cronobacter sakazakii. Both products are foods used for special medical purposes for infants. The products are mainly prescribed but are also available without a prescription.

Product details

Nutramigen LGG Stage 1 Hypoallergenic Formula
Pack size 400g
Batch code ZL3F7D
Best before 01 July 2025
Nutramigen LGG Stage 2 Hypoallergenic Formula
Pack size 400g
Batch code ZL3FAA
Best before 01 July 2025
Nutramigen LGG Stage 2 Hypoallergenic Formula
Pack size 400g
Batch code ZL3FDM
Best before 01 July 2025

Risk statement

The potential presence of Cronobacter sakazakii in the products listed above.

Symptoms caused by Cronobacter sakazakii usually include fever and diarrhoea, and in severe cases may lead to sepsis or meningitis which include symptoms in infants including poor feeding, irritability, temperature changes, jaundice (yellow skin and whites of the eyes) and abnormal breaths and movements.

Action taken by the company

Reckitt is recalling the above products and have contacted all stores and pharmacies that are supplying these products. The company has also issued a recall notice to its customers. These notices explain to customers why the products are being recalled and tells them what to do if they have bought the products. Please see the attached notice.

Our advice to consumers

If you have purchased or been prescribed any of the above product batches, do not feed it to your baby and return to the place of purchase. If you have additional questions, please contact Reckitt on 01895 230575. If you have any concerns about the health of your baby, please seek medical advice.

Slovakia – Unsuitable product Chilled chicken breast, DS: 02.12.2023Slovakia – Salmonella

SVPS

Unsuitable product Chilled chicken breast, DS: 02.12.2023

RVPS Rimavská Sobota carried out an official food inspection at the operator Tauris as, Potravinárska 6, 979 01 Rimavská Sobota, where on the basis of a targeted inspection (23/417) they took a sample of the raw material – Chilled chicken breast.

Product

  • Chicken breast, chilled
  • DS: 02.12.2023,
  • EAN: RW – 10471/23/PROD for microbiological criteria.
  • The country of origin of the raw material is Poland.

Finding

The supplied sample does not comply with the requirements of Commission Regulation (EC) No. 2073/2005 of November 15, 2005 of the European Parliament and the Council on microbiological criteria for food (OJ L 338), as amended, Chapter 1. Food safety criteria – 1.28: the presence of Salmonella Enteritidis bacteria was confirmed in the sample.

The raw material in question – chilled chicken breast – was processed into heat-treated meat products. The products are suspended for shipping and the supply of additional raw materials from the supplier from Poland has been suspended. Samples were taken for all incorporated products with objectionable raw materials and other randomly selected products, which were subsequently sent for microbiological examination to the appropriate laboratory.

USA – FDA – US Gulf Coast Trading Co., Inc. – Warning Letter

FDA

The United States Food and Drug Administration (FDA) inspected your refrigerated, frozen, and ambient food product warehouse located at 14100 Auto Park Way Ste. I, Houston, TX on August 7 through 15, 2023. During our inspection, FDA investigators found serious violations of the Current Good Manufacturing Practice, Hazard Analysis, and Risk-Based Preventive Controls for Human Food regulation (CGMP & PC rule) in Title 21, Code of Regulations, Part 117 (21 CFR part 117). At the conclusion of the inspection, FDA issued a Form FDA 483, Inspectional Observations, listing deviations found at your firm. In addition, during the inspection, FDA collected filth samples from various areas within your warehouse facility, and the analytical results revealed rodent filth present throughout your facility.

Based on FDA’s inspectional findings, we have determined that the food products warehoused in your facility are adulterated within the meaning of section 402(a)(3) of the Federal Food, Drug, and Cosmetic Act (the Act) [21 U.S.C. § 342(a)(3)] because they consist in whole or in part of any filthy, putrid, or decomposed substance, or are otherwise unfit for food, and section 402(a)(4) of the Act [21 U.S.C. § 342(a)(4)] because they were prepared, packed, or held under insanitary conditions whereby they may have become contaminated with filth, or whereby they may have been rendered injurious to health. You may find the Act and FDA regulations through links in FDA’s Internet home page at http://www.fda.gov.

France – FINE OYSTERS NORMANDY – Norovirus

Gov France

Product category
Food
Product subcategory
Fishing and aquaculture products
Product brand name
Cultimate Associated Producers
Model names or references
Caliber N°4 and N°3
Product identification
GTIN Batch Date
3700096607158 Packaging date: 12/24/23 Use-by date 03/01/2024
3700096607462 Packaging date: 12/24/23 Use-by date 03/01/2024
Packaging
1.5kg and 2kg
Start/end date of marketing
From 12/24/2023 to 01/03/2024
Storage temperature
Product to be stored at room temperature
Health mark
FR 14.312.120 CE
Geographical sales area
Whole France
Distributors
Lidl

USA- FDA Warning Letter- Lone Star Botanicals Inc.

FDA

The United States Food and Drug Administration (FDA) inspected your food manufacturing facility, located at 2001 Broussard St., Tyler TX 75701 on April 17-21, 2023. Your firm manufactures and repackages, among other food products, ready-to-eat (RTE) seasoning blends. During the inspection, the FDA investigator found serious violations of the Current Good Manufacturing Practice, Hazard Analysis, and Risk-Based Preventative Controls for Human Food regulation (CGMP & PC rule), Title 21, Code of Federal Regulations, Part 117 (21 CFR Part 117). At the conclusion of the inspection, FDA issued a Form FDA 483 (FDA- 483), Inspectional Observations, listing the deviations found at your firm. Based on FDA’s inspectional findings, we have determined that the ready-to-eat (RTE) seasoning products manufactured in your facility are adulterated within the meaning of section 402(a)(4) of the Federal Food, Drug, and Cosmetic Act (the Act) [21 U.S.C. § 342(a)(4)] in that they were prepared, packed, or held under insanitary conditions whereby they may have become contaminated with filth or rendered injurious to health. In addition, failure of the owner, operator, or agent in charge of a covered facility to comply with the Preventive Controls provisions of the CGMP & PC rule (located in Subparts A, C, D, E, F, and G of Part 117) is prohibited by section 301(uu) of the Act [21 U.S.C. § 331(uu)]. Further, we found significant violations of the labeling regulations for foods, 21 CFR Part 101. These violations cause  your seasoning blends and Dr. Botanical Health products to be misbranded within the meaning of section 403 of the Act (21 U.S.C. § 343).

France – MORBIER JURAMORBIER RAW MILK – Listeria monocytogenes

Gov France

Product category
Food
Product subcategory
Milk and dairy products
Product brand name
Arnaud Cheese Shop
Model names or references
Morbier Juramorbier Raw Milk
Product identification
GTIN Batch Date
02053730 139295 Use-by date between 12/19/2023 and 12/31/2023
02053120 139295 Use-by date between 12/19/2023 and 12/31/2023
02553730 139295 Use-by date between 12/19/2023 and 12/31/2023
02553120 139295 Use-by date between 12/19/2023 and 12/31/2023
Packaging
Under film
Start/end date of marketing
From 09/12/2023 to 21/12/2023
Storage temperature
Product to keep in the refrigerator
Health mark
FR 39-434-001 CE
Further information
Products sold self-service and in the traditional aisle
Geographical sales area
LOGELBACH WINTZENHEIM
Distributors
E. LECLERC WINTZENHEIM