Category Archives: Food Inspections

USA – FDA Investigation of Cronobacter Infections: Powdered Infant Formula (February 2022)

FDA

If you want to check if your powdered formula is part of the recall, you can enter the product lot code on the bottom of your package on the company’s websiteExternal Link Disclaimer.

If you have questions or need information about the recall, you can Submit Questions/Get Assistance.

If your infant is experiencing symptoms related to Cronobacter infection, such as poor feeding, irritability, temperature changes, jaundice, grunting breaths, or abnormal movements; contact your health care provider to report their symptoms and receive immediate care.

To report an illness or adverse event, you can

The FDA, along with CDC and state and local partners are investigating consumer complaints and/or reports of infant illness related to products from Abbott Nutrition’s Sturgis, MI facility. All of the ill patients are reported to have consumed powdered infant formula produced from Abbott Nutrition’s Sturgis, MI facility.

To provide clarity about which products are included in the Abbott Nutrition recall, FDA is publishing a full list of recalled brands  that have been included in the initial and expanded recall. Recalled products should no longer be available for sale, but if consumers have these products in their homes, they should check the lot code on the bottom of the package to determine if it is included in the recall.

The FDA is also providing additional information for parents and caregivers  of infants receiving medical specialty infant formula and individuals using certain medical foods.

We understand that infant formula is the sole source of nutrition for many infants and is an essential product. FDA is continuing to work with Abbott Nutrition to better assess the impacts of the recall and understand production capacity at other Abbott facilities that produce some of the impacted brands. We are also working with Abbott Nutrition on safe resumption of production at the Sturgis, MI facility. FDA is continuing to investigate and will update this advisory should additional consumer safety information become available.

Recommendation

The FDA is advising consumers not to use recalled Similac, Alimentum, or EleCare powdered infant formulas. Recalled products can be identified by the 7 to 9 digit code and expiration date on the bottom of the package (see image below). Products are included in the recall if they have all three items below:

  • the first two digits of the code are 22 through 37 and
  • the code on the container contains K8, SH, or Z2, and
  • the expiration date is 4-1-2022 (APR 2022) or later.

In addition to products described above, Abbott Nutrition has recalled Similac PM 60/40 with a lot code 27032K80 (can) / 27032K800 (case). At this time, Similac PM 60/40 with lot code 27032K80 (can) / 27032K800 (case) is the only type and lot of this specialty formula being recalled. Additional recall information for the initial recall is available on the FDA website. Parents can also enter their product lot code on the company’s websiteExternal Link Disclaimer to check if it is part of the recall.

Additional information for parents and caregivers of infants receiving medical specialty infant formulas and individuals using certain medical foods is available below.

Additional Information for Parents and Caregivers:

The recalls do not include liquid formula products.

Parents and caregivers should never dilute infant formula and should not make or feed homemade infant formula to infants. Consumers should also avoid purchasing imported formula through online sales, as it has the potential to be counterfeit.

If your regular formula is not available, contact your child’s healthcare provider for recommendations on changing feeding practices.

If you get infant formula through WIC, do not throw the formula out. Instead, you should take it to the store for a refund and exchange or call the company at 1-800-986-8540 to help you. WIC recipients should be able to obtain a different brand of similar formula. Call your local WIC clinic for more guidance. Also see:

More information on Cronobacter and infant formula is available on CDC’s website.

Recalled powdered infant formulas have the potential to be contaminated with Cronobacter, a bacterium that can cause severe foodborne illness primarily in infants. Cronobacter infections are rare but are especially high risk for newborn infants (see symptoms below).

Cronobacter bacteria can cause severe, life-threatening infections (sepsis) or meningitis (an inflammation of the membranes that protect the brain and spine). Symptoms of sepsis and meningitis may include poor feeding, irritability, temperature changes, jaundice (yellow skin and whites of the eyes), grunting breaths, and abnormal movements. Cronobacter infection may also cause bowel damage and may spread through the blood to other parts of the body.

If your child is experiencing any of these symptoms, you should notify your child’s healthcare provider and seek medical care for your child immediately. Healthcare providers and health departments are encouraged to report any confirmed cases of Cronobacter sakazakii to CDC.

Netherlands – Safety Warning Cocos Nucifera (Coconut Meat) – Salmonella

NVWA

Safety Warning Cocos Nucifera (Coconut Meat)

Importer Mooijer Volendam bv warns against coconut meat. Salmonella was found in the product. Do not eat the product.

Which product is it?

  • COCONUT MEAT / COCONUT MEAT / COCONUT MEAT / COCONUT MEAT, ‘Cocos Nucifera’, bag 250g (frozen)
  • Expiration date: August 2023
  • Barcode Number: 8716789014399

Website Mooijer Volendam bv

Yours sincerely

The Dutch Food and Consumer Product Safety Authority

France- Turkey roll with chorizo -Salmonella

Gov france

Identification information of the recalled product

  • Product category Food
  • Product subcategory Meats
  • Product brand name unbranded
  • Model names or references Turkey roll with chorizo
  • Identification of products
    GTIN Lot Dated
    2870119000000 sold at the traditional butcher’s stand Use-by date 03/11/2022
  • Marketing start/end date From 07/03/2022 to 10/03/2022
  • Storage temperature Product to be stored in the refrigerator
  • Geographic area of ​​sale fagnières
  • Distributors LECLERC-FAGNIERES

Practical information regarding the recall

  • Reason for recall Presence of salmonella
  • Risks incurred by the consumer Salmonella spp (causative agent of salmonellosis)

Germany – Coconut meat “Coconut Meat, Cocos Nucifera”, 250 g – Salmonella

LMW

11714980_1867503_Photo_Art-_2500_Coconut_250g_08-2023_Salmonella.jpg

Alert type:

Food

Date of first publication:

03/13/2022

Product name:

Coconut meat “Coconut Meat, Cocos Nucifera”, 250 g

ooijer Volendam bv NL
Reason for warning:

Detection of Salmonella

Packaging Unit: 250 g
Durability: 08/23
Lot identification: 8716789014399
Further information:

This food warning refers to the identical information from the Dutch authority for food and consumer product safety (NVWA)  ,  § 40 para. 2 sentence 3 LFGB.

salmonella

Salmonella disease manifests itself within a few days after infection with diarrhoea, abdominal pain and occasionally vomiting and a slight fever. The symptoms usually subside on their own after a few days. Babies, small children, senior citizens and people with a weakened immune system in particular can develop more severe illnesses. Anyone who has eaten this food and develops severe or persistent symptoms should seek medical attention and report possible salmonella infection.
It makes no sense to seek preventive medical treatment without symptoms.

France – Veal Escalope with Chanterelle Cream – Salmonella

Gov france

Identification information of the recalled product

  • Product category Food
  • Product subcategoryMeats
  • Product brand name E. Leclerc center in Gouesnou
  • Model names or references veal escalope with chanterelle cream
  • Identification of products
    GTIN Lot
    0200293000000 All lots
  • Marketing start/end date From 04/03/2022 to 08/03/2022
  • Storage temperature Product to be stored in the refrigerator
  • Health mark nil
  • Further information Product sold at the Butcher stand
  • Geographic area of ​​sale catchment area: Brest region
  • Distributors any

Practical information regarding the recall

  • Reason for recall presence of salmonella in 1 analysis

USA – FDA: Salmonella removed from Infant Formula Outbreak – Cronobacter sakazakii still cause of 4 illnesses with 2 deaths

Food Poison Journal

Total Adverse Events: 4
Hospitalizations: 4
Reported Deaths: 2
Illness Onset Date Range: 9/6/2021 – 1/4/2022
States with Adverse Events: MN (1), OH (2), TX (1)
Product Distribution: Nationwide and International

The FDA, along with CDC and state and local partners are investigating consumer complaints and/or reports of infant illness related to products from Abbott Nutrition’s Sturgis, MI facility. All of the ill patients are reported to have consumed powdered infant formula produced from Abbott Nutrition’s Sturgis, MI facility.

The Salmonella Newport illness previously included in this investigation of complaints and illnesses has been removed. In the early stages of this investigation, FDA included all consumer complaints of illness with exposure to products from the Sturgis, MI, facility. After further investigation, the FDA has determined that there is not enough information to definitively link this illness to powdered infant formula. CDC confirmed that this single Salmonella illness is not linked to an outbreak. The FDA and CDC are continuing to monitor for Salmonella cases and consumer complaints that may be related to this incident.

Cronobacter infection surveillance is not handled the same way as infection with more common foodborne pathogens, such as Salmonella or E. coli O157:H7. Cronobacter is not nationally notifiable and not reportable except in one state, which means doctors and labs are not required to report cases to their health department. Because Cronobacter is not a nationally notifiable pathogen, FDA relies on consumer complaints of illness sent to the Agency and on health care providers informing FDA directly about infants with Cronobacter infections. In addition, because Cronobacter is not nationally notifiable, whole genome sequencing (WGS) is rarely performed on these isolates. To date, no outbreaks of Cronobacter have been detected using WGS.

When single cases of Cronobacter are reported, the FDA conducts a thorough review of each complaint, conducts sampling of products, and initiates inspections as appropriate. FDA collaborates with CDC, which has developed a detailed questionnaire specifically for Cronobacter infections that is often used by state health departments in instances of Cronobacter sakazakii infection.

New Zealand – Gopals Paneer cheese recalled

MPI

11/03/2022

Food company Gopals Sweet & Snacks Limited is recalling its Gopala brand paneer cheese due to the possible presence of Listeria.

The pathogen was discovered through testing of product following 2 complaints of sickness.

New Zealand Food Safety deputy director general Vincent Arbuckle said the pathogens’ long incubation period made it difficult to establish a definitive link between the 2 cases and the product.

“However, because of the detection of Listeria in specific batches, we support the recall, and advise anyone who has bought paneer recently to take the precaution of checking the product date mark to see if it is affected.

“Importantly, cooking the paneer thoroughly until it is piping hot all the way through will kill the pathogen. People should not eat affected product raw.

“If you are in any doubt, please throw the product out or return it to the place it was purchased.

“Listeria poisoning (called listeriosis) can be serious in vulnerable people, including the young, the elderly, pregnant women and the immunocompromised.

“Healthy adults are likely to experience only mild infection, causing mild diarrhoea and flu-like symptoms.

Further information on Listeria

If you have consumed affected product and have any concerns about your health contact your health professional.

The affected product is all batches and dates up to and including best before 5 May 2022 of Gopala brand paneer cheese sold in packets of various weights between 300g and 1kg.

It is sold at Foodstuffs, Countdown and specific grocery stores throughout New Zealand.

This information is on our website’s recall page where we will post any updates about this recall as they come to hand.

Food recall: Gopala brand Paneer

As part of the recall process, New Zealand Food Safely will be working closely with Gopals Sweet & Snacks Limited to establish how the issue arose and what actions might be required to prevent it recurring.

RASFF Alert – Histamine – Tuna Fillet

RASFF

Histamine in Tuna fillet center cut from the Maldives in the Netherlands and Belgium

RASFF Alert – Pseudomonas fluorescens

RASFF

Burrata – Pseudomonas fluorescens – Italie in France

RASFF Alerts – Ochratoxin A – Nutmeg – Date Syrup

RASFF

Ochratoxin A content above the limit in Nutmeg from Indonesia in Hungary and Serbia

RASFF

Ochratoxin A in date syrup from Sweden in Germany