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Possible Listeria Contamination in Pork and Chicken

WASHINGTON, Nov. 1, 2017 - Chelsea Food Services, doing business as Journey Cuisine, a Denver, Colo. establishment, is recalling approximately 28,064 pounds of pork and chicken burritos and wrap products that may be adulterated with Listeria monocytogenes, the U.S. Department of Agriculture's Food Safety and Inspection Service (FSIS) announced today.

The ready-to-eat (RTE) pork and chicken burritos and wrap items were produced on various dates from Sept. 11, 2017 through Oct. 26, 2017. The following products are subject to recall:

8-lb. case containing 16 frozen burritos of "KING Soopers BACON BREAKFAST BURRITO" with "Sell By" dates from 03/11/18 to 4/26/18.

8-lb. case containing 16 frozen burritos of "KING Soopers CARNITAS POTATO BURRITO (Burrito Carnitas Caliente)" with "Sell By" dates from 03/11/18 to 4/26/18.

8-lb. case containing 16 frozen burritos of "KING Soopers CHICKEN QUESO BURRITO" with "Sell By" dates from 03/11/18 to 4/26/18.

8-lb. case containing 16 frozen burritos of "KING Soopers SPICY SAUSAGE BURRITO (Burrito Spicy Breakfast)" with "Sell By" dates from 03/11/18 to 4/26/18.

4-lb. case containing 8 sandwich kits of "SHAMROCK FOODS GRILLED CHICKEN WRAP" with "Use By" dates from 9/16/17 to 10/31/17.

The products subject to recall bear establishment number "EST. 19822" inside the USDA mark of inspection.

These items were shipped to retail locations in - Colorado - New Mexico - Utah - Wyoming

Journey Cuisine notified FSIS on Oct. 30, 2017 that one of its products, Burrito Carnitas Caliente, had tested positive for L. monocytogenes during the firm's product testing. After a review of the ingredients used in the Burrito Carnitas Caliente, the company determined that four additional products may be affected. There have been no confirmed reports of adverse reactions due to consumption of these products. 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.

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.

Children's Sleepwear, Violation of Federal Flammability Standard

Children's nightgowns and pajama sets

Hazard: The children's nightgowns and pajama sets fail to meet flammability standards for children's sleepwear, posing a risk of burn injuries to children. November 1, 2017

Recall number: 18-020

Consumer Contact: Little Mass at 800-977-9086 from 9 a.m. to 5 p.m. PT Monday through Friday, email at infolittlemass@gmail.com or teamlittlemass@gmail.com and online at www.littlemass.com and click on "Product Recall" at the bottom of the page for more information. Recall Details Description: This recall involves children's nightgowns and two-piece pajama sets. The sleepwear was sold in a variety of styles in sizes 7 through 14. Little Mass and style number T927S, T933, T935, T935S, T949, T952S or T953 are printed on a sewn-in side seam label.

Remedy: Consumers should immediately take the recalled sleepwear away from children and contact Little Mass for a full refund.

Uncompleted Auto Recall

By David Shepardson WASHINGTON (Reuters) - The U.S. National Highway Traffic Safety Administration said Friday it is funding a pilot program that will notify drivers in the state of Maryland if there are open, uncompleted recalls at the time that they register their vehicles. The government says only about 70 percent of auto safety recalls have led to repairs or resolution of the problematic issues.

Automakers, who have recalled record numbers of vehicles in recent years, have struggled to convince millions of owners of vehicles with potentially faulty Takata air bags to get the necessary repair work done. The number of U.S. vehicle recall campaigns hit a record high in 2016 for a third consecutive year, with 927 separate recalls affecting 53.2 million vehicles.

That total was bloated by recalls of Takata air bag inflators, which can rupture and send deadly metal fragments flying, and are already linked to 18 deaths and more than 180 injuries worldwide. Those recalls will eventually cover about 125 million inflators, representing the largest single auto safety recall ever for a single issue.

As of June, more than 65 percent of 46.2 million previously recalled Takata inflators in the United States had not been repaired. Congress gave NHTSA the authority to provide grant funding for up to six states that agreed to pilot programs to notify consumers of open recalls on their vehicles at the time of registration, but Maryland was the only state to apply.

"This first-in-the-nation grant will serve as an example to the rest of the country as we continue to work across government to reach consumers in new and creative ways with potentially life-saving information about their vehicles," Transportation Secretary Elaine Chao said in a statement.

Recalls jumped in 2014 after Congress held a series of hearings about major auto safety issues involving General Motors Co ignition switches and Takata air bags. In 2014, a record 63.95 million vehicles were recalled in the United

States -- more than twice the previous record set in 2004.

Some automakers, including Honda Motor Co, whose vehicles account for 17 of the 18 reported Takata-related deaths to date, are taking additional steps to locate vehicles with the potentially dangerous inflators. (Editing by Bernadette Baum)

Cosmetic "Gimme Brow" Eyebrow Gel Recall

Benefit Cosmetics Wants To Be Safe, Rather Than Sorry In a preemptive move to protect customers, Benefit Cosmetics recalled the latest batches of their tinted eyebrow volumizer. Customers who bought the Gimme Brow Gel eyebrow gel are urged to return the products in compliance with a voluntary recall issued by the cosmetics company. The company announced the recall in a statement that suggested the action was a precaution to avert any harm to customers. "If applied in its normal usage on the brows, the Gimme Brow product doesn't involve any risk," Benefit Cosmetics explained in their statement. "However, if it comes into contact with the eyes, it could lead to eye irritation." The company reported that there were just a few batches of the product that failed to meet quality standards. Even so, Benefit is pulling all of the products out of a concern for their customers, preferring to err on the side of caution. Every Gimme Brow Product Has Been Recalled An unnamed source, who was speaking on behalf of Benefit Cosmetics shared the details of the recall. The company has recalled every Gimme Brow product, including full size, samples, and any variation of the product that may be found in gift sets. The cosmetics company isn't leaving anything to chance, recalling everything that has recently come off of the line. The statement from Benefit Cosmetics also revealed that the recall is in effect for all countries in which their products are sold. Customers everywhere can return their Gimme Brow make-up for a full refund at the point of purchase. This includes Sephora and ULTA Beauty, as well as anyplace else the cosmetics were purchased. We recommend that you stop using the product. For a full refund of the Gimme Brow product, please return it to your original place of purchase. If you have additional questions contact us by email or phone: GimmeBrowInfo@benefitcosmetics.com +1-800-252-9218 (in the U.S. or Canada) +1-317-449-2302 (US Toll number for international calls)

Misbranded Salad with Chicken Products

Class II Recall 115-2017 Health Risk: Low Oct 28, 2017

Congressional and Public Affairs Maria Machuca (202) 720-9113 Press@fsis.usda.gov

WASHINGTON, Oct. 28, 2017 - Taylor Farms Florida, an Orlando, Fla. establishment, is recalling approximately 732 pounds of salads with chicken products due to misbranding and undeclared allergens, the U.S. Department of Agriculture's Food Safety and Inspection Service (FSIS) announced today.

The products contain fish (anchovies), a known allergen, which is not declared on the product label.

The ready-to-eat (RTE) salad with chicken items were produced and packaged on Oct. 22, 2017 and Oct. 23, 2107.

The following products are subject to recall: • 9.75-oz. plastic bowls containing "Taylor Farms American Style Pasta Salad" with a "USE BY 11/01/17" and case code of TFFLD 295 L5 EA.

• 9.75-oz. plastic bowls containing "Taylor Farms American Style Pasta Salad" with a "USE BY 11/02/17" and case code of TFFLD 296 L5 JP.

The products subject to recall bear establishment number "EST. 44818" inside the USDA mark of inspection. These items were shipped to retail locations in Florida.

The problem was discovered on Oct. 26, 2017, when Taylor Farms Florida received a consumer complaint about the taste of the salad dressing. After conducting an internal investigation, the firm determined that the products incorrectly contained Caesar salad dressing instead of Bacon Ranch salad dressing. The Caesar salad dressing contains anchovies.

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 who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.

Undeclared Allergen Chocolate Products

For Immediate Release

October 27, 2017

Contact

Consumers 248-486-0055

Announcement

View Product Photos

GKI Foods of Brighton, Michigan is recalling the following products:

Dark Chocolate Almond

Dark Chocolate Banana Chips

Dark Chocolate Blueberries

Dark Chocolate Almond Bark

Dark Chocolate Cashews

Dark Chocolate Cherries

Dark Chocolate Coconut

Dark Chocolate Coconut Almonds

Dark Chocolate Coffee Beans

Dark Chocolate Cranberries

Dark Chocolate Ginger

Dark Chocolate Peanuts

Dark Chocolate Pecans

Dark Chocolate Pineapple

Dark Chocolate Powerberry

Dark Chocolate Pretzel Balls

Dark Chocolate Raisins

Dark Chocolate Ginger Snap Cookies

Dark Chocolate Strawberries

Dark Chocolate Turbinado Sea Salt Almonds

Dark Chocolate Pretzel Nibs N/A

These products may contain an undeclared milk allergen. People who have an allergy or severe sensitivity to milk allergen run the risk of serious or life threatening allergic reaction If they consume these products.

Dark Chocolate Products were distributed in several states and they reached consumers through distributors and retail stores.

The products are packaged in plastic hanging and stand-up bags, plastic tubs, and cardboard boxes.

No Illnesses have been reported to date.

The recall was initiated after it was discovered that the Dark Chocolate Products containing the milk allergen were distributed in packaging that did not reveal the presence of the milk allergen.

Consumers who have purchased these products will be asked to return them to the place of purchase. Consumers with questions may contact the company at 248-486-0055