Recalls

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 infection can cause miscarriages and stillbirths among pregnant women. Any consumers concerned about an illness should contact a physician.

Products were distributed via the following retailers:

• Target: Good & Gather Organic Cherries and Berries Fruit Blend, Good & Gather Dark Sweet Whole Pitted Cherries, Good & Gather Mango Strawberry Blend, Good & Gather Mixed Fruit Blend, Good & Gather Mango Chunks, Good & Gather Blueberries, and Good & Gather Triple Berry Blend distributed nationwide from October 14, 2022 to May 22, 2023
• Aldi: Season’s Choice Tropical Blend distributed to select distribution centers or stores in AL, AR, CT, FL, GA, IA, KS, KY, MA, MD, MI, MO, MS, NC, NE, NH, NY, OH, OK, PA, RI, SC, TN, TX, VA, VT and WV from October 11, 2022 to May 22, 2023

Note that other stores are affected by this recall that are not in Georgia, refer to the link for the entire recall announcement. 

To date, there have been no illnesses associated with this voluntary recall.

This voluntary recall includes the following code dates currently in stores or consumers’ freezers:

Target

Good & Gather Organic Cherries and Berries Fruit Blend packaged in a 32-ounce plastic bag (3,961 cases) with the following codes:

FED305552 (Best By 2/24/2025)

Good & Gather Dark Sweet Whole Pitted Cherries packaged in a 12-ounce plastic bag (1,515 cases) with the following codes:

FED308862 (Best By 3/29/2025)

Good & Gather Mango Strawberry Blend packaged in a 48-ounce plastic bag (238 cases) with the following codes:

FED308351 (Best By 3/24/2025)

Good & Gather Mixed Fruit Blend packaged in a 48-ounce plastic bag (8,178 cases) with the following codes:

FED308153 (Best By 3/22/2025)

FED308251 (Best By 3/23/2025)

FED308951 (Best By 3/30/2025)

Good & Gather Mango Chunks packaged in a 12-ounce plastic bag (871 cases) with the following codes:

FED308661 (Best By 3/27/2025)

Good & Gather Blueberries packaged in a 48-ounce plastic bag (5,344 cases) with the following codes:

FED228651 (Best By 10/13/2023)

Good & Gather Triple Berry Blend packaged in a 48-ounce plastic bag (6,034 cases) with the following codes:

FED228652 (Best By 10/13/2023)

FED228751 (Best By 10/14/2023)

Aldi

Season’s Choice Tropical Blend and Mixed Fruit packaged in a 32-ounce plastic bag (38,909) with the following codes: 

FMX234011 (Best By 12/06/2024)

FMX234103 (Best By 12/07/2024)

FMX234211 (Best By 12/08/2024)

FMX303101 (Best By 1/31/2025)

FMX301402 (Best By 1/14/2025)

FMX230707 (Best By 11/03/2024)

FMX227705 (Best By 10/04/2024)

FMX235501 (Best By 12/21/2024)

FMX236001 (Best By 12/26/2024)

FMX236102 (Best By 12/27/2024)

FMX303201 (Best By 2/01/2025)

FMX303001 (Best By 1/30/2025)

FMX231804 (Best By 11/14/2024)

FMX236202 (Best By 12/28/2024)

FMX236301 (Best By 12/29/2024)

FMX301208 (Best By 1/12/2025)

FMX301302 (Best By 1/13/2025)

FMX230704 (Best By 11/03/2024)

FMX227605 (Best By 10/03/2024)

Consumers are urged to check their freezers for the recalled product, not to consume it and either discard the product or return it to the store for a full refund. All other Sunrise Growers products that have different lot codes or best by dates are not affected by this recall. The affected retail customers have been notified of this recall and instructed to remove any recalled product from retail store shelves and inventories.

Consumers seeking information may email recall@sunrisegrowers.com or call 1.888.490.5591 Monday through Friday, 8:00 a.m. to 5:00 p.m. Pacific Time.

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

Our commitment to food safety remains our utmost priority. Sunrise Growers has terminated all future business with the third-party supplier.

About SunOpta

SunOpta (Nasdaq:STKL) (TSX:SOY) is a U.S.-based, global pioneer fueling the future of sustainable, plant-based and fruit-based food and beverages. Founded nearly 50 years ago, SunOpta manufactures natural, organic and specialty products sold through retail and foodservice channels. SunOpta operates as a manufacturer for leading natural and private label brands, and also proudly produces its own brands, including SOWN®, Dream®, West Lifeâ„¢ and Sunrise Growers®. For more information, visit www.sunopta.comExternal Link Disclaimer and LinkedIn.

The frozen beef shepherd’s pie products were produced on March 1, 2023, with time stamps ranging between 17:45-17:56 hours. The following products are subject to recall:

• 4.31 lbs. cases of “MC Beef Shepherd’s Pie” with lot code 5006306020, BEST BY FEB 24 2024 and case code 2113100032, containing six 11.5 oz. carton packages of "Marie Callender’s BEEF SHEPHERD’S PIE” with lot code 5006306020 and BEST BY FEB 24 2024 on the side panel, with time stamps ranging between 17:45-17:56

The products subject to recall bear establishment number “EST 233” next to the USDA mark of inspection on the case and above the “BEST BY DATE” on the side panel of the individual product. These items were shipped to retail customer distribution centers in California, Colorado, Oregon, and Utah, and further distributed nationwide.

The problem was discovered when the firm received consumer complaints reporting pieces of clear, flexible plastic in the product, and notified FSIS of the situation. 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.

Consumers with questions about the recall can contact Conagra’s Consumer Care Hotline at 877-469-3783 or consumer.care@conagra.com. Members of the media with questions about the recall can contact Dan Hare, Sr. Director of Corporate Communications, Conagra at 312-549-5355 or Daniel.hare@conagra.com.

The recalled jelly cups were distributed nationwide in retail food stores and are sold in large clear jars. Below are the products being recalled:

1. Sun Wave Mini Fruit Jelly Cup (Assorted Flavors); UPC 715685121437; Net Weight 52.91 oz.
2. Sun Wave Mini Fruit Jelly Cup (Mango Flavor); UPC 715685121444; Net Weight 52.91 oz.
3. Sun Wave Mini Fruit Jelly Cup (Lychee Flavor); UPC 715685121451; Net Weight 52.91 oz.
4. Sun Wave Mini Fruit Jelly Cup (Assorted Flavors); UPC 715685121512; Net Weight 35.27 oz.
5. Sun Wave Mini Fruit Jelly Cup (Lychee Flavor); UPC 715685121529; Net Weight 35.27 oz.
6. Sun Wave Mini Fruit Jelly Cup (Mango Flavor); UPC 715685121536; Net Weight 35.27 oz

No incidents of consumers choking have been reported to date in connection with these products.

The potential choking hazard was confirmed after discussion with a representative from the Food and Drug Administration.

Consumers who have purchased the above products are urged to return them to the store of purchase for a full refund or dispose them in a sealed package inside a secure garbage can with a tight-fitting lid. For more information or inquiries, please contact the company at (626)-308-3212 Monday thru Friday between 9 am and 5 pm PST.

While the front of the affected jar is correctly labeled as Tostitos Avocado Salsa, the back of the jar is mislabeled with another product’s nutrition information and declarations. As a result, the allergen milk is not declared on the label.

The product covered by this recall was distributed nationwide at retail stores and via e-commerce channels. Consumers would have been able to purchase the jars as early as April 5, 2023. No other Tostitos products, flavors, sizes, or dip variety packs are recalled.

No allergic reactions related to this matter have been reported to date. If consumers have an allergy or severe sensitivity to milk, they should not consume the product and discard it immediately. Frito-Lay has informed the FDA of this action.

Consumers with the product described below can contact Frito-Lay Consumer Relations at 1-800-352-4477 (9 a.m. - 4:30 p.m. CST, Monday-Friday).

The specific recalled product information is listed below:

Product: Tostitos Avocado Salsa Dip packaged in a glass jar
Size: 15 oz. or 425.2 grams
UPC: UPC barcode ending in 0559
Best Before Date: Located on upper rim of jar: 2 NOV 2023 or 3 NOV 2023

Gelato Boy Chocolate Chunk was distributed nationwide and is sold at grocery stores, including but not limited to Sprouts Farmer’s Market, King Soopers / City Market, Whole Foods Market and others. The product can be found in the ice cream and novelties aisle.

The product is labeled “CHOCOLATE CHUNK GELATO” and comes in a 16 fl oz paper pint container with a lid. The affected Lot Code is 4043T2, with a Best By date of 04/25. The UPC is 853457008002.

No illnesses have been reported to date.

The recall was initiated after a customer notified Gelato Boy that the pint did not have its normal appearance and that it “tasted like there’s dairy in it”. Gelato Boy immediately located a pint with the same lot code and brought it to a lab for testing. It was confirmed that the product containing MILK was distributed in packaging that did not reveal the presence of MILK.

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

Customers with a MILK allergy or sensitivity who have purchased the affected product are urged not to consume the product and dispose of it or return it to their place of purchase for a full refund. Consumers with questions may contact the company at 720-548-0416, or at spoon@gelatoboy.com from 8am-4:30pm MST, Monday-Friday.

Restaurants and food retailers that have received shipments of frozen raw oysters, in half shell, Individual Quick Freezing (IQF), and block form, harvested between 2/10/2022 and 2/24/2022 and on 4/13/2022 and 4/14/2022 from Designated Area No. II, and exported by Dai One Food Co., Ltd., Republic of Korea (ROK).

Consumers, especially those who are or could become pregnant, the elderly, and persons with weakened immune systems, who have recently consumed raw oysters in Hawaii, Georgia, or Minnesota and suspect they have food poisoning should seek medical care immediately.

Frozen oysters harvested between 2/10/2022 and 2/24/2022 and on 4/13/2022 and 4/14/2022 from Designated Area No. II, Dai One Food Co., Ltd., ROK. The oysters were shipped from the ROK and distributed in Hawaii, Georgia, and Minnesota.

The Korean firm has voluntarily recalled frozen raw half shell oysters, frozen IQF oysters, and frozen oyster blocks harvested from Designated Area II harvest area between 2/10/2022 and 2/24/2022 and on 4/13/2022 and 4/14/2022 including lot numbers D021031, D021041, and D020481.

The U.S. Food and Drug Administration (FDA) is advising consumers not to eat, as well as restaurants along with food retailers not to sell, and to dispose of Dai One Food Co., Ltd., frozen raw half shell, IQF, and block form oysters with harvest dates between 2/10/2022 and 2/24/2022 and 4/13/2022 and 4/14/2022 from Designated Area No. II and sold in Hawaii, Georgia, and Minnesota.

The Hawaii Department of Health notified the FDA of five illnesses from individuals who consumed raw oyster shooters at a restaurant in Hawaii on 5/10/23. Traceback information revealed the source for the implicated raw oysters was from a shipment by Dai One Food Co., Ltd., ROK, harvested on 4/13/2022 and 4/14/2022 from Designated Area No. II. Samples collected from the 04/14/2022 harvest date were tested for the presence of norovirus. Norovirus GII was detected in one of the two samples collected. Further traceback information identified shipments from Dai One Food Co., Ltd., ROK of oysters harvested on 4/13 2022 and 4/14/2022 from Designated Area No. II were also distributed to Georgia.

In addition, the Minnesota Department of Health notified the FDA of five norovirus illnesses from individuals who consumed raw oysters at a restaurant in Minnesota on 6/3/2023 and 6/4/2023. Traceback information revealed the source for the implicated raw oysters was from a shipment by Dai One Food Co., Ltd., ROK, harvested between 2/10/2022 and 2/24/2022 in Designated Area No. II. These oysters were exported to a distributor in New York.

The FDA is issuing this alert advising consumers not to eat and restaurants and food retailers not to sell oysters harvested between 2/10/2022 and 2/24/2022 and on 4/13/2022 and 4/14/2022 from Designated Area No. II from Dai One Food Co., Ltd., in ROK, due to possible norovirus GII contamination. The FDA notified State Shellfish Authorities and the Interstate Shellfish Sanitation Conference (ISSC) of the import and harvest details.

As the FDA continues to monitor the investigation, we will provide additional information on further interstate distribution and provide assistance to states as needed. If contaminated oysters are found to have been distributed to additional states, we will update this public health alert. Please check back for more information.

Norovirus can cause a sporadic gastroenteritis, in populations ranging from children to the elderly. The infections are more frequent in children under age 5 than in adults. The most common symptoms of norovirus are diarrhea, vomiting, nausea, and stomach pain. Other symptoms include fever, headache, and body ache.

Most people infected with norovirus begin to develop symptoms 12 to 48 hours after infection. Symptoms usually last one to four days.

Restaurants and retailers should not sell the potentially affected raw oysters. Restaurants and retailers should dispose of any products by throwing them in the garbage or returning to their distributor for destruction.

• 5-lb. boilable plastic bags of “Gordon Choice® Homestyle Chili Topping” with lot code 230732002.

The product subject to recall bears establishment number “1917A” inside the USDA mark of inspection. This item was shipped to institutional and retail locations nationwide. The problem was discovered when the producing establishment notified FSIS that it had received a consumer complaint that bags labeled as homestyle chili topping contained beef taco filling. 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 institutional or consumers’ freezers. Consumers who have purchased these products are urged not to consume them and institutions are urged not to serve these products. These products should be thrown away or returned to the place of purchase.

The product can be identified as a 12 oz. glass bottle with orange sauce, called Texas Pete® Buffalo Wing Sauce. The only product affected has best used by 120623T 065239 printed on the cap of the product.

No illnesses have been reported as of May 25, 2023.

The recall was initiated after a report was received from a direct customer that a bottle labeled as Texas Pete® Buffalo Wing Sauce was located instead of Texas Pete® Extra Mild Wing Sauce. The bottle of Texas Pete® Buffalo Wing Sauce was missing the allergen declaration of soy. Investigation indicates the problem was caused by applying the wrong label during a portion of the production run.

Product was shipped to distribution centers and retail stores located in AL, CT, FL, GA, LA, MS, NC, NY, PA, SC, TN, TX & VA. Consumers with a soy allergy or sensitivity who have purchased Texas Pete Buffalo Wing Sauce with a best used by 120623T 065239 with a UPC 0 75500 10011 6 are urged not to consume the product and dispose of it or return it to their place of purchase for a full refund.

Consumers with questions may contact Mrs. Katerine Cardoso, Quality Assurance Manager at (336) 231-6417 Monday - Friday 8:00 am - 6:00 pm EST or email at ContactUs@garnerfoods.com.

The recalled products are distributed nationally in retail stores. The product comes in a 14-ounce reddish brown package with black lettering on the cup and lid, as reflected in the image below. The product is marked with lot number 23P102 (Best By Date April 12, 2025) which is displayed on the bottom of the pint. The recall does not apply to any other lot marking, best by date, or varieties of Van Leeuwen Ice Cream products.

The recall was voluntarily initiated after a customer complaint led to the discovery that the ice cream in this lot contains walnuts but was distributed in packaging that did not declare the presence of walnuts. The cause of the product labeling error is being investigated.

Consumers who have purchased the impacted lot should return them to the place of purchase for a full refund.

Any questions or concerns should be directed to JD Dillion, JD@vanleeuwenicecream.com or 215.824.6613 between the hours of 9:00 - 5:00 EST.

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.

AWG is a cooperative food wholesaler distributing to independently owned supermarkets. This recalled product was distributed from its Nashville Division only to independent retailers located in AL, GA, IN, KY, OH, TN, VA, and WV under the following retail banners: Belle Foods, Bellview Price Cutter, Booneville Shopwise, Brown County IGA, Buehler's, Buehler's Cash Saver, Buehler's IGA, Camridge City Market, Campbell's Market, Camron's Foodliner, Cash Saver, Cash Saver Harlan, Chappell's Hometown, Country Mart, Crossroads IGA, Food City, Food Giant, Food World, Foodland, Frabergs Foods, Fresh N Low, Gallion's Market, Gregerson's Cash Saver, Hilltop Cee Bee, Hometown IGA, Houchen's, Howard's IGA, Laurel Grocery Company, Liberty IGA, Market Place, Noble's IGA, Parkview IGA, Noble's IGA, Parkview IGA, Piggly Wiggly, Piggly Wiggly Warrior, Price Cutter, Price Less Foods, Price Less IGA, Quality Foods, Riesbeck's, Rivertown IGA, Simpson's Supermarket, Spencer Cash Saver, Stop to Save, Sureway, Sureway Henderson, Swafford and Sons IGA, Tietgens Mt. Pleasant IGA, Valu Market, Versailles IGA, Vevay IGA, Village Market & Café, Walnut Creek Country Market, Winburn Fruit Market, and Woodruff's Supermarket.

Consumers who purchased this product through these retail locations in these states are urged to check any product they may have at home. Consumers who purchased the product should look for the following Lot Codes and “use by” dates, which can be found on the bottom of the package.

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

Any consumers who purchased product with matching codes should discontinue use and dispose of the product. 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.