Recalls

Lot codes and best-by dates can be found on the upper portion of the glass bottle, above the label, printed in either black or orange directly on the glass bottle. Below are photos of affected labels.



The recall was initiated after it was discovered that the soy-containing product was distributed in packaging that did not explicitly reveal the presence of soy. Subsequent investigation indicates the problem was caused by a temporary breakdown in the company's production and packaging processes during a label redesign.



Production of the products with incorrect labels have been suspended and allergen information clearly disclosed on corrected labels.



Consumers who have purchased 5 fl ounce bottles of "Umami Everyday" or “Everything But The Sushi & Dumplings” are urged to return them to the place of purchase for a full refund or replacement.

• 1-lb. chubs containing “Bob Evans Italian Sausage” with lot code XEN3663466 and a “USE/FRZ BY” date of 11/26/22, with a time stamp between 14:43 and 15:25.

The products subject to recall bear establishment number “EST. 6785” inside the USDA mark of inspection. These items were shipped to retail locations nation-wide.

This voluntary recall is isolated to NESTLE© TOLL HOUSE© STUFFED Chocolate Chip Cookie Dough with Fudge Filling products that were produced between June and September 2022. These products were distributed in the continental United States and Puerto Rico.

No other Nestlé© Toll House products, including other NESTLE© TOLL HOUSE© STUFFED Cookie Dough and NESTLE© TOLL HOUSE© refrigerated cookie dough products, are impacted by this recall.

While no illnesses or injuries have been reported, we immediately took action out of an abundance of caution after a small number of consumers contacted Nestle© USA about this issue.

Consumers who may have purchased NESTLE© TOLL HOUSE© STUFFED Chocolate Chip Cookie Dough with Fudge Filling should not prepare or consume the product and should return the product to the retailer where it was purchased for a replacement or refund. For any further support needed, please contact Nestlé© USA at (800) 681-1676 Monday-Friday from 9 a.m.-6 p.m. EST.

We are working with the U.S. Food & Drug Administration (FDA) on this voluntary recall and will cooperate with them fully.

The quality, safety and integrity of our products remain our number one priority. We sincerely apologize for any inconvenience this action represents to both our consumers and retail customers.

The product was distributed nationwide in retail stores and through mail orders.

The recalled Hammond’s Salted Caramel Cookies are packaged in a 5-ounce printed cardstock box, with UPC -6 91355 89889 5. Hammond’s item number for this product is CK15008. The recalled product code, “Best By: 6/29/2023A" can be found on a sticker and it is located at the lower-right corner of the back of the box.



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

The recall was initiated after a routine product check revealed that peanut-containing product had been packed and distributed in incorrect packaging, which did not declare the presence of peanuts. Further investigation has determined the root cause to be a temporary failure of the manufacturer’s packing and product release process.



Consumers who have purchased 5-ounce packages of Salted Caramel Cookies from the described lot are urged to return them to the place of purchase for a full refund. Consumers with questions may contact Devon DeVries at Hammond’s Candies at 1-888-226-3999, Monday-Friday, 8am-4pm MST.

These products are being recalled because a small percentage of bottles (less than 1%) in the recalled lots have bottle caps that may not have sealed completely, which could result in spoilage. If spoiled product is consumed, gastrointestinal symptoms such as diarrhea and vomiting may occur.

This recall does not include any other liquid or powder formula brands or other nutrition products produced in our Columbus facility or elsewhere within our global nutrition manufacturing network. It also does not include any amino acid-based formulas or metabolic nutrition formulas.

This recall equates to less than one day's worth of the total number of ounces of infant formula fed in the U.S. and is not expected to impact the overall U.S. infant formula supply. Abbott is continuing production of Similac 2 fluid ounce/59 milliliter Ready-to-Feed liquid formula products for hospitals and healthcare providers' offices on a different production line. Similac infant formula will continue to be produced in alternative product sizes and formats for delivery to retail locations, in addition to increased production throughout our global manufacturing network.

The products included in the recall were distributed primarily to hospitals and to some doctors’ offices, distributors and retailers in the U.S., including Puerto Rico; one lot of products was sent to Barbados, Bermuda, Colombia, the Dominican Republic, Haiti, Jamaica, St. Croix and St. Thomas; and two lots were sent to Canada, Curacao, Panama, and Trinidad and Tobago.

Products were distributed as generic product without branding.



The affected products can be identified by:

Listeria monocytogenes is an organism that 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.

Products subject to the voluntary recall from Springfield, OH are identified by a product lot code beginning with the letter "W" and a "Best if Used By" date between December 22, 2021 and January 9, 2022. Products subject to the voluntary recall from Soledad, CA are identified by a product lot code beginning with the letter "B" and a "Best if Used By" date between December 23, 2021 and January 8, 2022. The product lot codes are located in the upper-right-hand corner of the package (see example below). Consumers who still have any of these products in their refrigerators are urged not to consume the product and to discard it immediately. No illnesses have been reported with the products being recalled to date.

This voluntary recall notification is being issued after harvest equipment used in the harvesting of the raw iceberg lettuce material used in these finished products was tested by Dole and found to contain Listeria monocytogenes.

Listing of products can be found here.

Recalled salad items from the Springfield facility were distributed in the states of AL, CO, CT, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, NC, NE, NY, OH, PA, SC, TN, VA and WI. Additionally, these salads were distributed in the following Canadian provinces: New Brunswick, Ontario, and Quebec. Recalled salad items from the Soledad facility were distributed in the states of AL, AZ, CA, CO, FL, GA, HI, IA, ID, IL, IN, KS, LA, MI, MN, MO, MS, MD, ND, NE, NV, NY, OK, OR, PA, TX, UT, VA, WA and WI. Additionally, these salads were distributed in the following Canadian provinces: Alberta, British Columbia, and Saskatchewan.

No other Dole products, including fresh fruit and field-packed fresh vegetables, are part of these voluntary recalls and are safe to consume.

Dole retailers have been advised to check store shelves and warehouse inventories to confirm that no recalled product is available for purchase by consumers.

Retailer and consumer questions about the voluntary recalls should be directed to the Dole Consumer Response Center at 800-356-3111, Monday-Friday, 8:00am to 3:00pm Pacific Time.

Dole Fresh Vegetables is coordinating closely with regulatory officials.

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 voluntarily recalled Earth Grown Vegan Traditional Falafel And Garlic & Herb Falafel Distributed & Sold Exclusively by Aldi, Batavia, IL were distributed in ALDI retail stores in the following states:  Alabama, Arizona, Arkansas, California, Connecticut,  Delaware, District of Columbia, Florida, Georgia, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Nebraska, New Hampshire, New Jersey, New York, North Carolina, North Dakota, Ohio, Oklahoma, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Virginia, West Virginia, and Wisconsin.

The product comes in a bag in a box marked with any of the following Lot numbers: 1472, 1481, 1531, 1532, 1541, 1552, 1561, 1581, 1601, 1611, 1612, 1661, 1682, 1732, 1752, 1762, 1782, 1802, and 1812, and would have been shipped to stores after June 24, 2021.  The lot number can be found in the “Best if used by” area on the outside flap of the box.  There has been no further production of this product.

There have been 20 reported cases in six (6) states (FL, IA, KS, MI, OH and WI) with onset dates reported between July 24, 2022 and September 19, 2022 with 5 hospitalization and no deaths.

Consumers who have purchased Earth Grown Vegan Traditional Falafel and Garlic & Herb Falafel Distributed & Sold Exclusively by Aldi, Batavia, IL with any of the above lot numbers after June 24, 2021, are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company Monday through Friday, 8:00 a.m. to 4:00 p.m. Eastern Time at 1-201-439-1036, Ext. 26.

The recalled "Angel Formula" was sold through it's Detroit, Michigan retail store and nationwide through online sales via www.moorherbs.com

The product is sold in 16 fl. Oz. plastic bottles and the labeling does not have any UPC or lot codes. We began shipping this product in February of 2019 and all units in distribution are included in this recall.

Parents and caregivers of infants who have purchased the recalled product should discontinue use and either throw the product away or return for a refund. Parents and caregivers of infants who have used these products and are concerned about the health of their child should contact their health care provider.

No illnesses or injuries have been reported to date. If you have any questions, call us at 313-583-9709.

This recall is being made at the request of the Food and Drug Administration. FDA Advisory