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Food Recalls

Company name: The Kroger Co
Brand name: Kroger
Product recalled: Bagged Kale Product
Reason of the recall: Listeria monocytogenes
FDA Recall date: September 16, 2021
Recall details: The Kroger Co. (NYSE: KR) is voluntarily recalling its 16-ounce Kroger bagged kale product, produced by Baker Farms, due to... See More possible listeria monocytogenes contamination. The products were distributed by Kroger grocery stores in the Columbus, Nashville and Atlanta Divisions, servicing Columbus and Toledo, OH; Knoxville, TN; eastern WV; and the states of GA, AL and SC.

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.

To date, we have not received any reports of illness related to the consumption of this bagged kale product.

This voluntary recall includes 16-ounce bags of Kroger branded Kale, with the UPC 11110-18170 with a best by date of 09-18-2021, which is printed on the front of the package below the light blue bar.

All affected products were pulled from our Produce departments on Sept. 16, 2021.

Customers who have purchased the affected product are urged to dispose of it or return it to their local store for a full refund.

Check the full recall details on fda.gov

Source: FDA
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Company name: Drew’s Organics, LLC
Brand name: Simply Nature
Product recalled: Organic Poppy Seed Dressing
Reason of the recall: Potential for microbial growth
FDA Recall date: September 16, 2021
Recall details: Drew’s Organics, LLC is voluntarily recalling one lot code of Aldi Simply Nature Organic Poppy Seed... See More Dressing due to a processing issue that could allow for microbial growth. Product has been distributed to select Aldi stores between August 20 and September 10 in the following states: AL, AZ, CA, CT, DE, GA, IA, IL, IN, KY, MA, MD, MI, MN, ND, NH, NJ, NY, OH, OK, PA, RI, SD, TN, TX, VA, VT, WI and WV.

The recalled product comes in a 12 fl. oz. glass bottle with the Best if Used By date of Feb 15 2023, and UPC #4099100023169.  The lot code is printed on the shoulder of the bottle above the label.

This action is being taken in cooperation with the US FDA. To date, no illnesses related to this product have been reported. No other Aldi products are affected by this recall.

The recall was initiated after Drew’s Organics, LLC observed a color difference in the Simply Nature Organic Poppy Seed Dressing after manufacturing.  Investigation revealed out of spec pH with the potential for microbial growth, including Clostridium botulinum, rendering it unsafe for consumption.

Consumers should discontinue use of this product and can return it to their place of purchase for a full refund.

Check the full recall details on fda.gov

Source: FDA
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The CFIA announced the recall of Jongilpoom brand Enoki Mushroom by Covic International Trading Inc.due to possible Listeria monocytogenes contamination. There have been no reported illnesses associated with the consumption of this product.

The recalled product is:
- Jongilpoom Enoki Mushroom (200 g), UPC: 8 807076 000321,... See More code: CE 158D

This product was distributed in Alberta and British Columbia.

If you have the recalled product in your home, please do not eat it, throw it away or returned it to the place of purchase.

In case you are experiencing listeria monocytogenes symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain, and diarrhea, it is important to report it. It can help to detect & resolve outbreaks early and prevent others from being harmed, and it enables better surveillance.

Check the full recall details on the CFIA website: inspection.canada.ca

Source: CFIA
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Company name: Buurma Farms Inc.
Brand name: Buurma
Product recalled: Plain (Flat Leaf) Parsley
Reason of the recall: May contain Shiga-toxin producing E.coli
FDA Recall date: September 15, 2021
Recall details: Buurma Farms Inc. of Willard, OH, is voluntarily recalling 320 boxes of its Plain Parsley after... See More testing showed possible contamination with Shiga-toxin producing E.coli. The product being recalled is Buurma Plain (flat leaf) Parsley with a harvest date of August 30, 2021 from their Gregory, Michigan location. A random, routine regulatory sample collected on 9/7/21 at a customer’s distribution center by the Michigan Department of Agriculture and Rural Development (MDARD) tested positive for non-O157 STEC (Shiga-toxin producing E. Coli) and reported 9/13/21. The sample is currently being genome sequenced to determine if it is pathogenic but out of an abundance of caution the product is being recalled.

Buurma Farms Inc. is coordinating closely with regulatory officials in connection with the recall. No illnesses have been reported to date.

Shiga-toxin-producing E. coli is an organism that can cause foodborne illness in a person who eats a food item contaminated with it. Symptoms of infection may include stomach cramps, diarrhea, and vomiting. The illness primarily impacts elderly individuals, children, and people with weakened immune systems. Most healthy adults and children rarely become seriously ill.

The product being recalled was harvested on August 30, 2021. It was sold and shipped in 30 count cartons to retailers in Ohio and Michigan between 8/31/21 and 9/3/21. It was also sold in 60 count crates to wholesalers in Illinois, Pennsylvania, New York, and South Carolina between 9/2/21 and 9/4/21.

Retailers and wholesalers can find the product code on the orange lot code sticker on each case and at the end of the GTIN number below the bar code on the PTI label. Only plain flat leaf parsley with a lot code of “2A242A6” and a PTI lot code of “2B243A6” is included in this recall. Retailers and wholesalers known to have received this product have already been contacted and asked to pull any potentially contaminated product from distribution. Individual bunches of flat parsley sold to retailers for purchase by consumers would likely have a “BUURMA FARMS Plain Parsley” twist-tie with a price look-up (PLU) number of 4901 and a UPC code of 33383 80125.

The PLU and UPC numbers are not unique to Buurma Farms and would be on all flat/plain parsley regardless of where it is from. The wholesale distribution channels involved in the recall do not have the twist-tie and instead have only a plain red rubber band on the bunch. No other plain leaf parsley is included in this recall. Production of the product involved has been suspended until FDA and other regulatory agencies have completed their investigation. The product involved should already be out of distribution but if consumers have any product they question, do not consume it, but rather discard it.

Check the full recall details on fda.gov

Source: FDA
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The CFIA announced the recall of Dairyland brand 1% Partly Skimmed Milk by Saputo Dairy Products Canada G.P. due to the presence of sanitizer residue.

The recalled product is:
- Dairyland 1% Partly Skimmed Milk, 4 L, UPC: 0 68700 01103 0, Best Before SE 21 4015.... See More This product was distributed in Alberta, Manitoba, and Saskatchewan.

If you have the recalled product in your home, please do not eat it, throw it away or returned it to the place of purchase.

In case you are experiencing food poisoning symptoms, it is important to report it. It can help to detect & resolve outbreaks early and prevent others from being harmed, and it enables better surveillance.

Check the full recall details on the CFIA website: inspection.canada.ca

Source: CFIA
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Company name: SEVIROLI FOODS, INC.
Brand name: H-E-B
Product recalled: Jumbo Stuffed Shells
Reason of the recall: Presence of foreign material (metal)
FDA Recall date: September 14, 2021
Recall details: Committed to the quality of its products and out of an abundance of caution, SEVIROLI FOODS, INC,... See More of Bellmawr, NJ is recalling H-E-B Jumbo Stuffed Shells - 22 oz due to potential presence of foreign material in product (Metal). Consumption of hard or sharp foreign material could cause physical injury. The affected products were distributed to H-E-B stores in Texas.

The issue was discovered on September 09, 2021, after H-E-B was notified of four customer complaints. All product related to this recall has been removed from H-E-B store shelves.

The following products, with the specific lot numbers, are subject to recall:

Item #: 796702
UPC #: 041220771110
Item Description: HEB Jumbo Stuffed Shells - 22 oz
Lot Code: 2 1208
Sell-by Date: 07/27/22

Code is located on the back of the back, upper left corner. 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 for a full refund.

Anyone concerned about an injury or illness should contact a healthcare provider.

Check the full recall details on fda.gov

Source: FDA
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Company name: Velvet Ice Cream
Brand name: Velvet
Product recalled: Raspberry Fudge Cordial Ice Cream
Reason of the recall: May contain undeclared peanuts
FDA Recall date: September 14, 2021
Recall details: Velvet Ice Cream has issued a voluntary recall of its 56oz Raspberry Fudge Cordial Ice Cream... See More because it may contain undeclared peanuts. People who have an allergy or severe sensitivity to peanuts could experience a serious or life-threatening allergic reaction if they consume this product.

The impacted product was distributed to retail stores in Ohio, Kentucky, Indiana and West Virginia starting in late July with a production date of July 14, 2021. The affected product can be identified by UPC 0-7068210049-7 and the following codes printed on the bottom of the carton: A2 19521 26-012 and To date, there are no reported illnesses associated with this recall.

Velvet was notified of the issue by a single customer and has since learned that the cause of the error has been traced to a third-party manufacturer packaging error. One carton has been affected at the time of this release. Velvet Ice Cream is committed to the safety of its products and is conducting this recall in full cooperation with the Food and Drug Administration.

Customers who have purchased the affected product should dispose of it immediately or return it to the retailer where it was purchased.

Check the full recall details on fda.gov

Source: FDA
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The FSIS announced the recall of approximately 3,768 pounds of beef and chicken empanada products by SAS Foods Enterprises Inc that were produced without the benefit of federal inspection and bearing a label with a false USDA mark of inspection. These products were shipped to retail consignees... See More in IL, IN, MN, OH and WI.

The recalled products are:
- 1-lb. zip-lock bags or clear, plastic containers with “SAS Food EMPANADAS DE POLLO CHICKEN PATTIES.”
- 1-lb. zip-lock bags or clear, plastic containers with “SAS Food EMPANADAS DE CARNE BEEF PATTIES.”

These products were produced on various dates from Jan. 1, 2020 through Sept. 11.

There have been no confirmed reports of adverse reactions due to consumption of these products.

FSIS is concerned that some products may be frozen and in consumers’ freezers. If you have the recalled products in your home, please do not eat them, throw them away or returned them to the place of purchase.

In case you are experiencing food poisoning symptoms, it is important to report it. It can help to detect & resolve outbreaks early and prevent others from being harmed, and it enables better surveillance.

For more information, please check on FSIS website: fsis.usda.gov

Source: FSIS
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Company name: McKee Foods
Brand name: Little Debbie®
Product recalled: Mini Nutty Buddy Cookie Bites Sandwich Cookies
Reason of the recall: Undeclared pecans
FDA Recall date: September 11, 2021
Recall details: McKee Foods of Collegedale, Tenn., is recalling 25 cases of Little Debbie® Mini Nutty Buddy Cookie... See More Bites Sandwich Cookies, because they may contain undeclared pecans. People who have an allergy or severe sensitivity to pecans run the risk of serious or life-threatening allergic reaction if they consume these products.

This recall does not impact Little Debbie® Nutty Buddy® Wafer Bars or any other Little Debbie products. Little Debbie® Mini Nutty Buddy Mini Cookie Bites Sandwich Cookies are sold in individual bags with a product weight of 2.5 oz.  The only products covered by this recall have best-by dates of Dec. 24 and Dec. 25, 2021 as shown below.

The covered Little Debbie® Mini Nutty Buddy Cookie Bites Sandwich Cookies were distributed through retail stores in the following locations:

- Kentucky: Jackson, Columbia, Somerset, and surrounding areas
- North Carolina: High Point, Greensboro, Asheville, Clemmons, and surrounding areas
- Tennessee: Sweetwater, Jackson, Piney Flats, Lebanon, Powell Crossroad, Knoxville, Maryville, Clarksville, Morristown, Crossville, Nashville, Collegedale, and surrounding areas

No illnesses have been reported to date.

The recall was initiated after it was discovered that product containing pecans was included in packaging that did not reveal the presence of tree nuts. Subsequent investigation indicates the problem was caused by a temporary breakdown in the production processes of the contract manufacturer that makes and packages the product for McKee Foods.

Consumers who have purchased these Little Debbie® Mini Nutty Buddy Cookie Bites Sandwich Cookies from the geographic areas listed above may contact the company at 1-800-422-4499 with the package code information for refunds, Mon.-Thurs., 8:30 a.m.-6 p.m., and Fri., 8:30 a.m.-4 p.m. ET.

Check the full recall details on fda.gov

Source: FDA
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Company name: Dole Fresh Vegetables, Inc.
Brand name: Dole
Product recalled: Curly leaf parsley
Reason of the recall: Non-O157 Shiga-toxin producing E. coli
FDA Recall date: September 10, 2021
Recall details: Monterey, California – September 10, 2021 – Dole Fresh Vegetables, Inc. is voluntarily recalling a limited... See More number of cases of conventional Curly Leaf Parsley. The product being recalled is Dole® Curly Leaf Parsley, with harvest dates of August 18, 2021, and August 19, 2021.  A random, routine regulatory sample collected in Michigan tested positive for non-O157 STEC (Shigatoxin-producing E. coli).

Dole Fresh Vegetables is coordinating closely with regulatory officials in connection with the Recall; no illnesses have been reported.  Shiga-toxin-producing E. coli  is an organism that can cause foodborne illness in a person who eats a food item contaminated with it. Symptoms of infection may include stomach cramps, diarrhea, and vomiting. The illness primarily impacts elderly individuals, children, and people with weakened immune systems. Most healthy adults and children rarely become seriously ill.

The product was distributed to retail stores, wholesalers, and distributors in two pack sizes – 60-count (74 cases) and 30-count (39 cases). Retailers, wholesalers, and distributors can find the product code in the lower right portion of the PTI label.  The product code for both the 60 count cases and the 30 count cases is 0 07143 000310 3.  Individual bunches of parsley purchased by consumers have a price look-up (PLU) number on binding twist-ties of 4899 and a UPC code of 0 3383 80330 0. The Curly Leaf Parsley subject to this Recall was distributed in FL, IA, MI, MN, and MO.

This precautionary recall is being initiated due to a positive non-O157 STEC result found on a single sample collected by the Michigan Department of Agriculture during routine random sampling. Only conventional Curly Leaf Parsley harvested on the dates noted above bearing the specific PLU and UPC code found on the bunches and PTI label codes found on the cases are included in this Recall. 

No other Curly Leaf Parsley items are included in the Recall.  Consumers who have any product with these UPC/PLU Product Codes should not consume it, but rather discard it. Retailers and consumers with questions may call the Dole Consumer Center  at 1-800-356-3111, which is open Monday-Friday 8am-3pm PST.

Check the full recall details on fda.gov

Source: FDA
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