Reckitt, a producer of nutrition products, announced today that, out of an abundance of caution, it has chosen to voluntarily recall two (2) select batches of ProSobee 12.9 oz. Simply Plant-Based Infant Formula due to a possibility of cross-contamination with Cronobacter sakazakii. All product distributed went through extensive testing and tested negative for the bacteria.

ProSobee Simply Plant-Based Infant Formula in 12.9 oz containers was manufactured between August 2022 and September 2022. The products were distributed through retail stores nationwide in the U.S., Guam, and Puerto Rico. The batches in question can be identified by the number on the bottom of the can. Recalled product batches are ZL2HZF and ZL2HZZ both with a UPC Code of 300871214415 and a “Use By Date” of “1 Mar 2024.”  The recall involves approximately 145,000 cans.

No other ProSobee Simply Plant-Based Infant Formula batches or other Reckitt products are impacted.

No illnesses or adverse events have been reported. If parents have any questions, they should consult with their pediatrician or contact us at 1-800-479-0551 24/7 or by email at consumer.relations@rb.com

We are committed to the highest level of quality and safety and it is for this reason that we have taken this extraordinary measure. The batches in question tested negative for Cronobacter and other bacteria and this is an isolated situation. After a thorough investigation, we have identified the root cause, which was linked to a material from a third party. We have taken all appropriate corrective actions, including no longer sourcing this material from the supplier.

The health and safety of infants is our highest priority. All of our products undergo rigorous and industry leading quality tests and checks to ensure that they meet or exceed all standards set by regulatory bodies, including the World Health Organization and the U.S. Food and Drug Administration. It is for this reason that we have the highest level of confidence in the safety and quality of every infant formula we make.

What Consumers Should Do if They Purchased This Product

Consumers who purchased ProSobee Simply Plant-Based Infant Formula should check the bottom of the can to identify whether the batch number is affected. Product with batch codes ZL2HZF and ZL2HZZ both with a UPC Code of 300871214415 and a “Use By Date” of “1 Mar 2024” should be disposed of or returned to the place of purchase for a total refund. You can also contact us at 800-479-0551 or by email at consumer.relations@rb.com and we will help verify if this product was impacted.

If you have any concerns, contact your health care provider. For more information please visit us at www.enfamil.comExternal Link Disclaimer

https://urldefense.com/v3/__https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/reckitt-recalls-two-batches-prosobee-129-oz-simply-plant-based-infant-formula-because-possible__;!!EErPFA7f–AJOw!AOODke3TUisgfOs0W2eWUR70JOuDOHTvUde1Ma0oNZHb12R-pc_dgC0jHLeqsnFcccvPF0H57Q2WBjAVPB6Jj8IrFeWiwho$

Silvestri Sweets Inc. of Geneva, IL is voluntarily recalling its 8 ounce bags of Favorite Day branded Valentine’s Milk Chocolate Covered Caramels with Nonpareils because they may contain an undeclared tree nut.  People who have allergies to tree nuts {chestnuts, brazil nuts, walnuts, hazelnuts, pecans, pine nuts, cashews} run the risk of serious or life-threatening allergic reaction if they consume these products.

The recalled items were distributed nationwide through Target retail stores.

The products are packed in 8 oz. Favorite Day branded stand up pouch bags with the lot # 33822 and best by date on 07 DEC 2023, which are printed on the back of the bag underneath the UPC barcode.

No illnesses have been reported to date in connection with this problem.

The recall was initiated after it was discovered that possible tree nut inclusions were distributed in packaging and/or product that did not reveal the presence of tree nuts. Subsequent investigation indicates the problem may have been caused by a temporary breakdown in the company’s production and packaging process.

Consumers who have purchased 8 ounce bags of the Favorite Day Valentine’s Milk Chocolate Caramels with nonpareils are urged to call Target Guest Relations at 1-800-440-0680 (24/7) for a refund.

Consumers with questions may contact Silvestri Sweets at 1-630-232-2500 – M-F 8:30am-4:30pm CST.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/silvestri-sweets-issues-voluntary-allergy-alert-undeclared-pecan-milk-chocolate-caramels

Wismettac Asian Foods, Inc., Santa Fe Springs, CA is recalling 10.58 oz packages of Shirakiku brand Spice Seasoning products (Spice Ichimi Togarashi 300g and Spice Shichimi Togarashi 300g). The product package of Ichimi spice seasoning contains Shichimi spice seasoning contents (incorrect package) causing the undeclared allergen of sesame seeds. The outer carton of “Ichimi” and “Shichimi” may possibly contains inner packages of “Ichimi”, and the inner packages contain “Shichimi” contents.

People who have an allergy or severe sensitivity to seasame run the risk of serious or life-threatening allergic reaction if they consume these products.

The product was distributed in AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, Il, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, NH, NJ, NV, NY, OH, OK, OR, PA, RI, SC, TN, TX, VA, WA, WI, WV mainly through restaurants and some through retail stores.

The product comes in a 10.58 oz, clear plastic bag. The affected lot code specified on the package is 12262023, distributed between June 27, 2022 and February 8, 2023. The UPC for the product is 074410341169

No illnesses have been reported to date in connection with this issue.

The recall was initiated after it was discovered that the product containing sesame was distributed in packaging that did not reveal the presence of sesame. Subsequent investigation indicates the problem was caused by a human error during the packing process.

The distribution of the product has been ceased until the company is certain that the problem has been corrected.

Consumers who have purchased the product are urged to return them to the place of purchase for a full refund.

Consumers with questions may contact the company at recall@wismettacusa.com.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/wismettac-asian-foods-issues-allergy-alert-undeclared-spice-seasoning

Two Rivers Coffee of South Plainfield, NJ is voluntarily recalling its peanut butter single serve hot chocolate pods distributed as “Brooklyn Bean Peanut Butter Cup Hot Cocoa”, “Pingo Peanut Butter Cookie Hot Chocolate” and “Cold Stone Peanut Butter Cup Perfection” in 12 count, 40count, and 100 count boxes produced from January 2021 to November 2022, due to an undeclared peanut allergen in an ingredient from Two Rivers Coffee’s raw material supplier that was not disclosed to Two Rivers Coffee or its licensors. People who have an allergy or severe sensitivity to peanuts may run the risk of serious or life-threatening allergic reaction if they consume these products.

Recalled products were distributed nationwide through retail stores and online orders.

This voluntary recall affects only the peanut butter single serve hot chocolate pods mentioned above which were included in the following products that have the best by dates of January 2022 through December 2024:

No other Two Rivers Coffee single serve pods are part of this recall.

To date, no illnesses or allergic reactions have been reported in connection with these products.

All peanut butter hot chocolate single serve pods manufactured after January 20th, 2023 are properly labeled in regard to allergen information. This is a voluntary action taken by Two Rivers Coffee with the knowledge of the FDA.

Consumers with a peanut allergy who have in their possession the affected products are urged not to consume the product. Consumers that have any of the single serve pods mentioned above should contact the place of purchase for a replacement or refund.

The quality and safety of our products is our number one priority. Although this occurred through a non-disclosure by an unaffiliated ingredient supplier to our company and not through our own fault, we still must take this matter very seriously.

Consumers with questions may contact the company at (800) 418-0689 Monday –Thursday 9:00 am to 4:00 PM or email us at support@tworiversco.com.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/two-rivers-coffee-issues-allergy-alert-undeclared-peanut-allergen-peanut-butter-hot-chocolate

Daniele International LLC, a Mapleville, R.I., establishment, is recalling approximately 69,255 pounds of ready-to-eat (RTE) sausage products that may be adulterated with Listeria monocytogenes

The RTE sausage products were produced on various dates from May 23, 2022, through November 25, 2022, and shipped to retail locations nationwide on various dates from December 23, 2022, through January 17, 2023. The following products are subject to recall [view labels]:

• 6-oz. plastic tray of “FREDERIK’S by meijer SPANISH STYLE charcuterie sampler tray” with sell by date 4/15/23.
• 6-oz. plastic tray of “Boar’s Head CHARCUTUERIE TRIO” with sell by dates 4/13/23, 4/14/23, and 4/15/23.
• 7-oz. plastic tray of “COLAMECO’S PRIMO NATURALE GENOA UNCURED SALAMI” with sell by dates 12/22/23, 12/30/23, and 1/17/24.
• 7-oz. plastic tray of “COLAMECO’S PRIMO NATURALE BLACK PEPPER UNCURED SALAMI” with sell by date 12/23/23.
• 1-lb. plastic tray of “DEL DUCA SOPRESSATA, COPPA & GENOA SALAMI” with sell by dates 4/13/23, 4/14/23, 5/03/23, and 5/04/23.
• 1-lb. plastic tray of “DEL DUCA CALABRESE, PROSCIUTTO & COPPA” with sell by dates 5/6/23 and 5/13/23.
• 1-lb. plastic tray of “DEL DUCA GENOA SALAMI, UNCURED PEPPERONI & HARD SALAMI” with use by dates 3/25/23, 3/26/23, and 5/4/23.
• 12-oz. plastic tray of “Gourmet Selection SOPRESSATA, CAPOCOLLO, HARD SALAME” with sell by date 4/14/23.

The products subject to recall bear establishment number “EST. 54” inside the USDA mark of inspection. These items were shipped to retail locations nationwide.

FSIS discovered the problem during routine inspection activities where Listeria monocytogenes was found on surfaces in which the product came into contact.

There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.

Consumption of food contaminated with L. monocytogenes can cause listeriosis, a serious infection that primarily affects older adults, persons with weakened immune systems, and pregnant women and their newborns. Less commonly, persons outside these risk groups are affected.

Listeriosis can cause fever, muscle aches, headache, stiff neck, confusion, loss of balance and convulsions sometimes preceded by diarrhea or other gastrointestinal symptoms. An invasive infection spreads beyond the gastrointestinal tract. In pregnant women, the infection can cause miscarriages, stillbirths, premature delivery or life-threatening infection of the newborn. In addition, serious and sometimes fatal infections in older adults and persons with weakened immune systems. Listeriosis is treated with antibiotics. Persons in the higher-risk categories who experience flu-like symptoms within two months after eating contaminated food should seek medical care and tell the health care provider about eating the contaminated food.

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.

https://www.fsis.usda.gov/recalls-alerts/daniele-international-llc-recalls-ready-eat-sausage-products-due-possible-listeria

Utopia Foods Inc of Glendale, NY, is expanding the recall of its 200g packages of “Enoki Mushrooms”, imported from China, with clear and blue plastic packages with clear markings of “Best before 03/02/2023” or “Best before 03.09.23” distributed between January 6th to January 13th, 2023 because they have 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.

The product comes in a 200g, clear and blue plastic package with brand name “UTOPIA” and bar code 8928918610017 marked on the packaging.

No illnesses have been reported to date in connection with this problem.

The recalled “Enoki Mushrooms” were distributed in NY, NJ and CT to produce wholesale companies.

The distribution of the product has been suspended while FDA and the company continue to investigate the source of the problem.

All vendors who have distributed the 200g packages of “Enoki Mushrooms” should immediately cease the distribution and notify their customers of the recall and recall instructions. If their customers have further distributed the product notify them to instruct their customers.

Consumers who have purchased the item are urged to return them to the place of purchase for a refund.

Consumers with questions may contact the company at 718.389.8898.

If you have any questions regarding this listserve, please contact 573-751-6095 Bureau of Environmental Health Services

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/utopia-foods-expands-recall-enoki-mushrooms-because-possible-health-risk

GFA Production (Xiamen) Co., Ltd. Issues Voluntary Nationwide Recall of Easy Care First Aid® Burn Cream and First Aid Kits Due to Microbial Contamination

December 23, 2022 – Xiamen, Fujian, GFA Production (Xiamen) Co., Ltd. is voluntarily recalling one lot of Easy Care first aid® AfterBurn ® Cream, 0.9 g single-use packets.  The single use packets are sold in boxes of 10 or packaged in certain First Aid kits. This recall is to the consumer level. FDA analysis found the product to be contaminated with Bacillus licheniformis, and Bacillus sonorensis.

Risk Statement: In immunocompromised patients, the topical use of the contaminated Easy Care® AfterBurn® Cream 0.9g single-use packets could potentially result in severe or life-threatening adverse events such as bacteremia, sepsis, and peritonitis. In non-immunocompromised patients, the population most likely to use the product, the use of the defective product may result in infectious complications, for instance skin infections, but in this population the infections are expected to be less severe and more readily responsive to treatment. To date, GFA Production (Xiamen) Co., Ltd. has not received any reports of adverse events related to this recall.

The Easy Care first aid® AfterBurn® Cream 0.9 g single-use packet, is used as an over the counter first-aid treatment for minor burns. The single use packets bear lot number W06I28 and are  packaged in boxes of ten or included in the certain First Aid kits named below.  The lot number of the single use packet can be found on the back of the packet.  The lot number for the First Aid Kit that contains the single use packet can be found on each kit, either on the product hang-tag or on the bottom of the kit. The product was distributed nationwide to retailers from March 4, 2022 through December 12, 2022.  Refer to the images below for guidance on where to find the lot code details.  If your product does not have a lot code that is listed in the below table then it is not part of this recall and can be used as intended.

GFA Production (Xiamen) Co., Ltd. is notifying its distributor by e-mail and is arranging for the return of all recalled Easy Care first aid® AfterBurn® Cream, .9g single-use packets and the certain First Aid kits that contain them.  Retailers that have any 0.9 g single-use packets or the First Aid kit lots listed above should return them to their distributor. Consumers should stop using the Easy Care first aid® AfterBurn® Cream .9g single-use packet and discard it.

Consumers with questions regarding this recall can contact the U.S. distributor, Adventure Ready Brands, by email to regulatory@adventurereadybrands.com or telephone to 603-837-0285 on Monday to Friday from 9:00AM and 5:00PM, Eastern Time. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/gfa-production-xiamen-co-ltd-issues-voluntary-nationwide-recall-easy-care-first-aidr-burn-cream-and

12/12/22:   Byheart Issues Voluntary Recall of Five Batches of Its Infant Formula Because of Possible Health Risk

Company Announcement

None of the distributed ByHeart product has tested positive for any contaminants

No consumer complaints received, to date, that would indicate any illness

Recall is not related to ByHeart’s own manufacturing facility in Reading, PA in any way; facility continues to run 24/7; re-stock expected in January

ByHeartExternal Link Disclaimer, a next-generation baby nutrition company, announced today that, out of an abundance of caution, it has chosen to voluntarily recall five batches of ByHeart Whole Nutrition Infant Formula due to the potential for cross-contamination with Cronobacter sakazakii. No distributed ByHeart product has tested positive for the bacteria.

The product being recalled is ByHeart Whole Nutrition Infant Formula, Milk Based Powder with Iron for 0-12 Months in 24 oz containers. The formula under voluntary recall was distributed directly to consumers in the U.S. and can be identified by the number on the bottom of the can. Recalled product batches are 22273 C1, 22276 C1, 22277 C1, 22278 C1, and 22280 C1 printed with use by 01 JAN 24 or 01JUL 24.

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.

It is important to note that this recall is not related to ByHeart’s own manufacturing in any way. In addition, the company has not received any consumer complaints that would indicate any illness, to date; illness complaints are an early detection of safety concerns. If a baby has already consumed all of the formula, there is no reason for concern, and no additional action is needed. If parents have any questions, they should consult with their pediatrician.

ByHeart owns its entire manufacturing supply chain with the exception of final canning, which is conducted by a reputable third-party packager. ByHeart is taking this precautionary measure because one test sample collected from the third-party packaging facility tested positive for Cronobacter sakazakii. All product packaged that day, and the first production on the next day, was isolated for destruction and not distributed. Out of an abundance of caution, we are now recalling all product produced during the entire production run.

As a company committed to parents, ByHeart holds itself to the highest standards when it comes to safety and applauds the FDA’s efforts to oversee the safe manufacturing of infant formula. Parents can remain confident in the safety of ByHeart’s products as the company continues to expand its investments in infant formula innovation, clinical studies, and industry-leading quality standards. ByHeart’s manufacturing facility in Reading, PA, continues to operate 24/7, and the company is committed to providing customers formula in January.

What ByHeart Customers Should Do

Customers who purchased ByHeart product should check the bottom of the can and dispose of product from batches 22273 C1, 22276 C1, 22277 C1, 22278 C1, and 22280 C1. ByHeart is setting up a webpage at https://byheart.com/noticesExternal Link Disclaimer with additional information about its measures. Should customers have any other questions or want to find out if the product they have is included in the voluntary recall, please email notices@byheart.com or text ByHeart at 1-909-506-2354. The company will also be reaching out directly to all customers via email who purchased orders from these identified batches.

ByHeart knows that formula is critical to a baby’s health and growth and wants to make sure that all customers have what they need to keep their baby fed and healthy, no matter what brand of formula they use. While ByHeart works 24/7 to meet the demand for formula, the fastest way the company can replace the formula customers purchased is to cover the cost of two cans of alternate formula. Additionally, affected customers will receive two cans of their next order of ByHeart Whole Nutrition Formula for free.

If your infant is experiencing symptoms related to Cronobacter infection, contact your health care provider to report their symptoms and receive immediate care. To report an illness or adverse event, you can

• Call an FDA Consumer Complaint Coordinator if you wish to speak directly to a person about your problem.
• Complete an electronic Voluntary MedWatch form online.
• Complete a paper Voluntary MedWatch form that can be mailed to the FDA.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/byheart-issues-voluntary-recall-five-batches-its-infant-formula-because-possible-health-risk

The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert due to concerns that fully cooked summer sausage products may be contaminated with extraneous materials, specifically plastic. A recall was not requested because the products are no longer available for purchase.
The fully cooked summer sausage products were produced on July 13, 2022. The following products subject to the public health alert are [view labels]:      

1-lb. chubs containing “JET HIGH PRAIRIE MEATS SUMMER SAUSAGE” with lot code 220715 represented on the label.
1-lb. chubs containing “FANTASMA’S finest SUMMER SAUSAGE” with lot code 220715 represented on the label.

The products bear establishment number “EST. 31865” inside the USDA mark of inspection. These items were shipped to retail locations in Kansas and Missouri and additional locations through online sales.

The problem was discovered when the firm notified FSIS that they received a customer complaint reporting clear plastic embedded within multiple packages of summer sausage products.

There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider. 

FSIS is concerned that some product may be in consumers’ refrigerators or freezers. 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.

Media and consumers with questions regarding the recall can contact Louis Fantasma, Paradise Locker Meats Plant Manager, at 816-945-9278 or louis@paradisemeats.com.
Consumers with food safety questions can call the toll-free USDA Meat and Poultry Hotline at 888-MPHotline (888-674-6854) or live chat via Ask USDA from 10 a.m. to 6 p.m. (Eastern Time) Monday through Friday. Consumers can also browse food safety messages at Ask USDA 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/.

https://www.fsis.usda.gov/recalls-alerts/fsis-issues-public-health-alert-fully-cooked-summer-sausage-products-due-possible