Recalls

The product was distributed in CA, CO, AZ, GA through retail stores.

The products come in a 19.04 oz, illustrated plastic bag. The UPC for the product is 074410455453 which is located on the back side of the package. This issue affects all lot codes or date codes.

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

The recall was initiated after we found out that the product contains undeclared allergen (skipjack tuna: fish). Subsequent investigation indicates the problem was caused by a human error during the label design making process.

The last distribution of the product in the marketplace was in January 2023.

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.

People who have allergies to milk run the risk of serious or life-threatening allergic reaction if they consume these products.



The recalled Salento Organics products were distributed nationwide in retail stores and through mail orders.

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

The recall was initiated after it was discovered that the milk-containing product was distributed in packaging that did not reveal the presence of milk.

Subsequent investigation indicates the problem was caused by a temporary breakdown in the company's production and packaging processes.

Production of the product has been suspended until FDA and the company are certain that the problem has been corrected.

Consumers who have purchased 4 ounce packages of Dark Chocolate Fruit and Peanut Bites, listed above are urged to return them to the place of purchase for a full refund.

Consumers with questions may contact the company at hello@salentorganics.com or calling at 561-402-8232, operational hours 9am EST - 5pm EST.

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

The recalled Gluten Free Reese’s Pieces Brownie Brittle were distributed nationwide in retail stores and through online orders.

The product comes in a 4-ounce pouch UPC 711747011562 marked with lot codes SG 1054 15/NOV/2023 1S and SG 1054 15/NOV/2023 2S on the backside of pouch.

One illness has been reported to date in connection with this problem, to date.

The recall was initiated after it was discovered that the gluten-containing product was distributed in packaging that did not reveal the presence of wheat. Subsequent investigation indicates the problem was caused by cross-contamination at a co-manufacturer, resulting in undeclared wheat in the product.

Production of the product has been suspended until FDA and the company are certain that the problem has been corrected.

Consumers who have purchased 4-ounce packages of Gluten Free Reese’s Pieces Brownie Brittle with lot codes SG 1054 15/NOV/2023 1S and SG 1054 15/NOV/2023 2S should not consume the product and should contact Brownie Brittle for a full refund.

Consumers may contact the company by calling at (800) 651-7263 Monday-Friday from 8:30AM - 5:00PM EST or via email at recall@browniebrittle.com Second Nature Brands is conducting this recall with the full knowledge and cooperation of the U.S. Food and Drug Administration.

Hepatitis A is a contagious liver disease that results from exposure to the Hepatitis A virus, including from food. It can range from a mild illness lasting a few weeks to a serious illness lasting several months. In rare cases, particularly consumers who have a pre-existing severe illness or are immune compromised, Hepatitis A infection can progress to liver failure.

Illness occurs within 15 to 50 days of exposure and includes fatigue, abdominal pain, jaundice, abnormal liver tests, dark urine, and pale stool. Hepatitis A vaccination can prevent illness if given within two weeks of exposure to a contaminated food. Persons who may have consumed affected product should consult with their health care professional or local health department to determine if a vaccination is appropriate, and consumers with symptoms of Hepatitis A should contact their health care professionals or the local health department immediately.

The following products are subject to this recall. The lot codes and best by dates are found on the back of each bag (see attached pictures below):

Although Hepatitis A has not been detected on this product, out of an abundance of caution, consumers should stop consuming the product and return it to their local store for a refund. 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.

All inventories of the affected lot should be removed from sale. Consumers who have purchased the products are urged to destroy or return it to the place of purchase for a full refund. Consumers with questions may contact the company at customer.service@scenicfruit.com

Importantly, no distributed product has tested positive for the presence of this bacteria, no adverse events have been reported and no other products manufactured at this facility or any other of Perrigo’s facilities are affected by this recall.

Cronobacter sakazakii is a bacteria commonly found in the environment. In most people it causes no symptoms but in some, particularly premature infants, infants under 2 months of age or infants with weakened immune systems fever, poor feeding, excessive crying or low energy as well as other serious symptoms can occur.

This product is sold at retailers across the U.S. Consumers who purchased the product after March 5, 2023 should look for the following Lot Codes and “use by” dates, which can be found on the bottom of the package. No other lot codes are impacted by this recall. Any consumers who purchased product with matching codes should discontinue use and dispose of the product.

Gerber® Good Start® SootheProTM 12.4 oz:



300357651Z - USE BY 04JUL2024



300457651Z - USE BY 05JUL2024



300557651Z - USE BY 06JUL2024



300557652Z - USE BY 06JUL2024



300757651Z - USE BY 08JUL2024



300857651Z - USE BY 09JUL2024



301057651Z - USE BY 11JUL2024



301057652Z - USE BY 11JUL2024



301157651Z - USE BY 12JUL2024



Gerber® Good Start® SootheProTM 30.6 oz:



301357652Z - USE BY 14JUL2024



301457652Z - USE BY 15JUL2024



301557651Z - USE BY 16JUL2024



Gerber® Good Start® SootheProTM 19.4 oz:



301557652Z - USE BY 16JUL2024I

Consumers can request refunds for impacted products and find more information about Gerber® Good Start® by contacting the Gerber Parent Resource Center on behalf of Perrigo at 1-800-777-7690 anytime 24/7. Consumers with any health-related questions should contact their healthcare provider.

This recall is being conducted in consultation with the U.S. Food and Drug Administration (FDA).

For over 130 years, Perrigo has been committed to meeting the needs of consumers—and the quality and safety of our products is our highest priority. We have numerous regulatory approved procedures throughout the manufacturing process to control for Cronobacter sakazakii. Every batch of infant formula is tested to make certain it meets stringent nutritional, safety, quality, and regulatory requirements. As part of our rigorous protocols to protect the safety of families and infants, we are proactively taking this action.

About Perrigo

Perrigo Company plc is a leading provider of Consumer Self-Care Products and over-the-counter (OTC) health and wellness solutions that enhance individual well-being by empowering consumers to proactively prevent or treat conditions that can be self-managed. Visit Perrigo online at www.perrigo.com.

On November 1, 2022, Perrigo acquired Nestle©'s Gateway Eau Claire, Wisconsin, plant, along with the U.S. and Canadian rights to the Good Start® infant formula brand. Perrigo operates the Good Start® infant formula brand in the United States and Canada while Nestle© operates the Good Start® infant formula brand for Women Infants and Children (WIC) contracts.

Media Contact Tim Schramm, (908) 370-4771, E-mail: tschramm@coynepr.com

The impacted product comes in a single-serving box with UPC Code 854021008152, Lot Number 048C2023 and an expiration date of 4/30/2023 stamped on the side of the box.

Strawberry Granola & Greek Yogurt Parfait Bar is the only product impacted. No other products are being recalled. No illnesses have been reported to date.

This potential limited exposure was found at a third-party manufacturer’s facility where Parfait Bars are produced. The third-party manufacturer does not manufacture any other Clio products. Clio does not manufacture Parfait bars at its own facility.

The recall was the result of a routine testing program by the company which revealed that affected Strawberry Parfait product produced by Clio’s contract manufacturer may contain Listeria monocytogenes. The third-party manufacturer has ceased production and Clio has ceased distribution of the affected product while the FDA and the company continue their investigation into what caused the problem.

Consumers who have purchased Clio Strawberry Granola & Yogurt Parfait bar with an expiration date of 4/30/2023 should not consume the product and are urged to return it to the place of purchase for a full refund or to destroy the recalled product.



Consumers with questions may contact the company at 1-908-505-2546 (Monday – Friday, 9-5pm EST).

Listeria 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 monocytogenes infection can cause miscarriages and stillbirths among pregnant women.

This voluntary recall includes all units of the ready-to-eat Tapas branded Cocktail Shrimp by Lidl, packaged in 7 oz. containers, that may still be in customers’ possession. Affected products will have a UPC of 4056489411499. All product codes currently on the market are subject to the recall.

The recall was issued as a result of routine testing, which revealed that the finished product contained the bacteria. Lidl performs this testing on an ongoing basis to help ensure safe and quality products for our customers. Lidl US has ceased the production and distribution of the product as we continue our investigation in conjunction with the FDA to resolve the issue. Lidl US has received no reports or complaints of illness related to this product to date.

If customers have purchased this product, they should not consume the product, and immediately return it to their nearest Lidl store for a full refund. Customers who have questions about this voluntary recall should call the Lidl US Customer Care Hotline at (844)-747-5435 (8 am-8 pm ET, Monday-Saturday).

The health and safety of our customers is our top priority. Lidl US regrets any inconvenience related to this voluntary recall. Our Quality Assurance Department is constantly working to ensure that all products on our shelves meet the high-quality standards that we would expect when feeding our own families. We are grateful for all our Lidl US customers who choose to shop with us every day.

The recalled Sugar Free Peanut Butter Cups were distributed nationwide to wholesale and retail stores. The recalled Sugar Free Peanut Butter Cups are packaged in a 2.4 oz plastic bag, and they are labeled with Best Before dates of 01MAY23 and 01JUN23 and UPC of 077260096937 with Lot code(s): K0521, K0321, K0421, L2122, L2221, L2321. The lot code and best before date can be found on the back of the product packaging, below the UPC.

The recall was initiated following consumer contacts regarding the wrong product inside the outer packaging for Sugar Free Peanut Butter Cups product.  Russell Stover has received no reports of any illness or allergic reactions related to this issue to date.

An error by the firm’s 3rd party co-packing company resulted in individually-wrapped Sugar Free Pecan Delight products being placed in the outer packaging for Sugar Free Peanut Butter Cups. The inner packaging correctly identifies the products as Sugar Free Pecan Delights and the physical Sugar Free Pecan Delight product appears distinct from the Sugar Free Peanut Butter Cup product.

Consumers who may have purchased this product may contact Russell Stover Chocolates directly for a voucher or replacement product. If you have any questions, please contact Russell Stover Chocolates on our website using the Contact Us Form at https://www.russellstover.com/contact-us

On February 24, 2023, the Florida Department of Agriculture and Consumer Services closed shellfish harvesting area FL-3012 for the harvest of wild oysters and initiated a recall of these wild oysters harvested from December 16, 2022, to February 24, 2023.

Do not eat oysters included in this recall.

Individuals should be aware of the current elevated risk of illness associated with raw oyster consumption. Consumption of food contaminated with Salmonella can cause salmonellosis. The most common symptoms of salmonellosis are diarrhea, abdominal cramps, and fever within 12 to 72 hours after eating a contaminated product. Most people recover without treatment.

In rare circumstances, infection can produce more severe illness and require hospitalization. Older adults, infants, pregnant women, and immunocompromised individuals are at higher risk of developing a severe illness and should seek medical attention if symptoms arise.

For more information regarding this recall, please visit the Florida Department of Agriculture and Consumer Services website at https://www.fdacs.gov/Divisions-Offices/Aquaculture.