Category Archives: Food Inspections

Ireland – Recall of Specific Batches of EleCare Similac and Alimentum Similac due to the Possible Presence of Salmonella and Cronobacter sakazakii

FSAI

Monday, 21 February 2022

Elecare

Alimentum

Summary
Category 1: For Action
Alert Notification: 2022.14
Product: Please see table below
Batch Code: Please see table below
Country Of Origin: United States

Message:

Abbott is recalling specific batches of its EleCare Similac and Alimentum Similac due to the possible presence of Salmonella and Cronobacter sakazakii. No products distributed to Ireland have tested positive for the presence of Cronobacter sakazakii or Salmonella Newport. Both products are foods used for special medical purposes for infants, ordinarily to be used under medical supervision. Point-of-sale recall notices will be displayed in stores supplied with the implicated batches.

Nature Of Danger:

Salmonella and Cronobacter sakazakii can cause illness in infants if they are present in powdered infant formula. Although Cronobacter sakazakii and Salmonella cannot grow in powdered infant formula, they can survive for a long period of time and therefore, pose a potential risk after rehydration if the product is temperature abused. Contamination of powdered infant formula with Cronobacter sakazakii and Salmonella can cause severe disease in infants such as diarrhoea (sometimes bloody), fever, sepsis or meningitis which can lead to serious neurological and developmental issues and can be fatal on rare occasions. Sepsis and meningitis may include poor feeding, irritability, temperature changes, jaundice (yellow skin and whites of the eyes) and abnormal breaths and movements. Among infants, those at greatest risk for infection are neonates (<28 days), particularly pre-term infants, low-birth weight infants or immunocompromised infants.

Action Required:

Manufacturers, wholesalers, distributors, caterers & retailers:

Retailers are requested to remove the implicated batches from sale and to display a point-of-sale recall notice in stores where the affected batches were sold.

Consumers:

Parents and guardians are advised not to feed the implicated batches to infants.

Table of implicated Abbott products

France – Auchan – Garlic and Fine Herbs Smoked Ham Bites – Listeria monocytogenes

Gov france

Identification information of the recalled product

  • Product category Food
  • Product subcategory Others
  • Product brand name AUCHAN
  • Model names or references Auchan Les Bouchées Smoked Ham Garlic and Fine Herbs 100 g
  • Identification of products
    GTIN Lot Dated
    3596710439607 229 Use-by date 03/24/2022
  • Packaging Plastic tray 100 g
  • Marketing start/end date From 02/11/2022 to 02/18/2022
  • Storage temperature Product to be stored in the refrigerator
  • Health mark EN 88.321.001 EC
  • Geographic area of ​​sale Whole France
  • Distributors AUCHAN

Practical information regarding the recall

  • Reason for recall Presence of Listeria monocytogenes
  • Risks incurred by the consumer Listeria monocytogenes (causative agent of listeriosis)

France – Liver Cream – Listeria monocytogenes

Gov france

liver cream sold in the traditional delicatessen section of the Carrefour Market Essars store between February 8 and February 9, 2022

Brand: unbranded

  • Ref. Form :2022-02-0286
  • Version №:1
  • Origin of the sheet: CSF CARREFOUR-MARKET ESSARS
  • Legal nature of the recall: Voluntary

Identification information of the recalled product

  • Product category Food
  • Product subcategory Meats
  • Product brand name unbranded
  • Model names or references liver cream sold in the traditional delicatessen section of the Carrefour Market Essars store between February 8 and February 9, 2022
  • Identification of products
    GTIN Lot
    1111111111111 sold between February 8 and February 9, 2022
  • Packaging sold by the cut, packed in food foil in a bag
  • Marketing start/end date From 08/02/2022 to 09/02/2022
  • Storage temperature Product to be stored in the refrigerator
  • Further information  liver cream sold in the traditional delicatessen section of the Carrefour Market Essars store between February 8 and February 9, 2022
  • Geographic area of ​​sale ONLY CARREFOUR MARKET ESSARS
  • Distributors ONLY CARREFOUR MARKET ESSARS

Practical information regarding the recall

  • Reason for recall suspected listeria monocytogenes
  • Risks incurred by the consumer Listeria monocytogenes (causative agent of listeriosis)

France – SAINT NECTAIRE FARMER Cheese – Listeria monocytogenes

Gov france

Identification information of the recalled product

  • Product category Food
  • Product subcategory Milk and dairy products
  • Product brand name ARVERNE
  • Model names or references SAINT NECTAIRE FARMER L’ARVERNE
  • Identification of products
    Lot Dated
    63VBM040122 Date of minimum durability 03/24/2022
  • Marketing start/end date From 08/02/2022 to 16/02/2022
  • Storage temperature Product to be stored in the refrigerator
  • Health mark63-335-004
  • Geographic area of ​​sale Departments: PUY-DE-DOME (63)
  • Distributors FRUITIER OF BALLAINVILLIERS / SMALL CHABRELOCHE CASINO

Practical information regarding the recall

  • Reason for recall PRESENCE LISTERIA MONOCYTOGENES
  • Risks incurred by the consumer Listeria monocytogenes (causative agent of listeriosis)

Research – What is Cronobacter sakazakii, formerly Enterobacter sakazakii? And, why it is a risk to babies in powered formula

Food Poison Journal

Enterobacter sakazakii was first described as a new bacterial species in 1980, and over a hundred scientific papers have been written about it. From 1980 to 2007 it was known as Enterobacter sakazakii, but in 2007 there was a proposal to reclassify it into a new genus Cronobacter as Cronobacter sakazakii. (1) For simplicity and for the reasons mentioned later, this discussion will continue to use the original name Enterobacter sakazakii. The proposed alternative classification is given as a section at the end and includes a discussion of the problems and the need for future studies.

Enterobacter sakazakii is a Gram-negative rod-shaped bacterium classified in the family Enterobacteriaceae. It has been isolated from three types of infection — devastating meningitis in very young babies (neonates), bacteremia (blood steam infection) in older babies, and a wide variety of infections (or colonization) in older babies, children and adults. The majority of infections reported in the peer-reviewed literature have described neonates—newborn infants, including premature infants, post-mature infants, and full-term newborns—with sepsis, meningitis, or necrotizing enterocolitis. (2) Although it has been isolated from cases of necrotizing enterocolitis, its causative role is unclear. (3)

Reported outcomes in neonatal meningitis are often severe: seizures; brain abscess; hydrocephalus; developmental delay; and death in as many as 40%–80% of cases. Premature infants are thought to be at greater risk than more mature infants, other children, or adults, and outbreaks have occurred in hospital units for newborns. (3)

Although E. sakazakii can cause illness in all age groups, infants are believed to be at greatest risk of infection and E. sakazakii was first implicated in a case of neonatal meningitis in 1958 (before the organism was given a scientific name). Since that time, around 70 cases of E. sakazakii infection have been reported, but it is likely that is the number of cases is significantly under-reported in all countries and the incidence is probably higher. (4)

USA – Baby formula recalled after 4 infants in 3 states fall ill

Washington Post

The FDA says the powered formulas were linked to bacterial infections and made at a Michigan plant.

The four cases occurred in Ohio, Minnesota and Texas. However, FDA press officer Veronika Pfaeffle said the formulas made at the Sturgis facility “can be found across the United States and were likely exported to other countries as well.”

Cronobacter is a bacteria that can cause severe infections, including inflammation of the membrane surrounding the brain and spinal cord, known as meningitis. Its symptoms include poor feeding, irritability, temperature changes, jaundice, labored breathing and abnormal movements. Salmonella can cause digestive illness and fever, commonly presenting itself in the form of diarrhea, fever and abdominal cramps. Both conditions can be life-threatening for children.

Belgium – Golden Sun brand Basmati rice – Aflatoxin B1

AFSCA

LT Foods recall
Product: Golden Sun brand Basmati rice.
Problem: Aflatoxin B1 content too high.
LT Foods has decided, in agreement with the FASFC, to withdraw the product Basmati Rice (1 kg) of the Golden Sun brand from sale and to recall it from consumers because of an excessively high aflatoxin B1 content.

We ask that you do not consume this product and return it to your point of sale. You will be reimbursed even without presenting the receipt. Product description: – Product name: Basmati rice – Brand: Golden Sun – Best before date (BDD): 06/10/2023 – EAN code: 20364625

– Sale period: from 08/10/2021 to 18/02 /2022 – Type of packaging: plastic packaging (bag) – Weight: 1 kg The product was distributed in Belgium by Lidl.

For any further information , contact Lidl customer service ( 0800/73520 (free))

USA – FDA Alerts the Public to Potentially Contaminated Products from Family Dollar Stores in Six States – Salmonella

FDA

For Immediate Release:

Today, the U.S. Food and Drug Administration is alerting the public that several categories of FDA-regulated products purchased from Jan. 1, 2021, through the present from Family Dollar stores in Alabama, Arkansas, Louisiana, Mississippi, Missouri and Tennessee may be unsafe for consumers to use. The impacted products originated from the company’s distribution facility in West Memphis, Arkansas, where an FDA inspection found insanitary conditions, including a rodent infestation, that could cause many of the products to become contaminated. The FDA is working with the company to initiate a voluntary recallExternal Link Disclaimer of the affected products.

“Families rely on stores like Family Dollar for products such as food and medicine. They deserve products that are safe,” said Associate Commissioner for Regulatory Affairs Judith McMeekin, Pharm.D. “No one should be subjected to products stored in the kind of unacceptable conditions that we found in this Family Dollar distribution facility. These conditions appear to be violations of federal law that could put families’ health at risk. We will continue to work to protect consumers.”

This alert covers FDA-regulated products purchased from Family Dollar stores in those six states from Jan. 1, 2021, through the present. Some examples of these products include human foods (including dietary supplements (vitamin, herbal and mineral supplements)), cosmetics (skincare products, baby oils, lipsticks, shampoos, baby wipes), animal foods (kibble, pet treats, wild bird seed), medical devices (feminine hygiene products, surgical masks, contact lens cleaning solutions, bandages, nasal care products) and over-the-counter (OTC) medications (pain medications, eye drops, dental products, antacids, other medications for both adults and children).

Consumers are advised not to use and to contact the company regarding impacted products. The agency is also advising that all drugs, medical devices, cosmetics and dietary supplements, regardless of packaging, be discarded. Food in non-permeable packaging (such as undamaged glass or all-metal cans) may be suitable for use if thoroughly cleaned and sanitized. Consumers should wash their hands immediately after handling any products from the affected Family Dollar stores.

Consumers who recently purchased affected products should contact a health care professional immediately if they have health concerns after using or handling impacted products. Rodent contamination may cause Salmonella and infectious diseases, which may pose the greatest risk to infants, children, pregnant women, the elderly and immunocompromised people.

Following a consumer complaint, the FDA began an investigation of the Family Dollar distribution facility in West Memphis, Arkansas, in January 2022. Family Dollar ceased distribution of products within days of the FDA inspection team’s arrival on-site and the inspection concluded on Feb. 11. Conditions observed during the inspection included live rodents, dead rodents in various states of decay, rodent feces and urine, evidence of gnawing, nesting and rodent odors throughout the facility, dead birds and bird droppings, and products stored in conditions that did not protect against contamination. More than 1,100 dead rodents were recovered from the facility following a fumigation at the facility in January 2022. Additionally, a review of the company’s internal records also indicated the collection of more than 2,300 rodents between Mar. 29 and Sep. 17, 2021, demonstrating a history of infestation.

Related Information

USA – Giant Eagle Diced Green Peppers Recalled For Possible Listeria monocytogenes

Food Poisoning Bulletin

There are two recalls for Giant Eagle Diced Green Peppers on the FDA’s Enforcement Report page. These recalls have not been posted on the FDA’s recall web page. And they do not appear on Giant Eagle’s recall page.

The first recall is for Giant Eagle Diced Green Peppers that are packaged in 10 ounce (283 gram) bags. The product is frozen. There are 12 packages per case. The best by date for this product is 10/14/2023. No UPC number has been provided for this product. The recalling firm is Giant Eagle Inc. at 101 Kappa Drive in Pittsburgh.

The second recall is for Giant Eagle Diced Green Peppers that are also packaged in 10 ounce poly bags. There are 12 10 ounce bags per case, and the product is also in 22 pound cartons. The code information on this product is: R16372 exp. 03/12/2023 R16514 exp. 09/30/2022 R17422 exp. 01/21/2023 R17117 exp. 08/12/2023 R17133 exp. 04/14/2023 R18388 exp. 10/14/2023. There is no UPC number given for this product. The recalling firm is Frozen Food Development at 156 W. Harrisburg Avenue in Rheems, Pennsylvania.

Romania – Salam Verona / Raw, dried salami and Salam Picantella / Salami Listeria monocytogenes

 SC MONTANA POPA SRL recalls Salam Picantella / Salami (Lot L155627012022; Expiry date 27.04.2022) due to Listeria monocytogenes contamination.

SC La Meseni SRL recalls Salam Verona / Raw, dried salami (300g; Lot 13; Expiry date 01.05.2022) due to Listeria monocytogenes contamination.