K A S H R U T . C O M_©

Frito-Lay Issues Voluntary Allergy Alert on Undeclared Milk in Lay’s Lightly Salted Barbecue Flavored Potato Chips

June 14, 2019 from the FDA

Frito-Lay today issued a limited voluntary recall of 7 3/4 oz. bags of Lay’s Lightly Salted Barbecue Flavored Potato Chips because they may contain undeclared milk ingredients.

The products covered by this recall were distributed in retail locations in the following states: Arkansas, Arizona, California, Colorado, Idaho, Iowa, Kansas, Louisiana, Minnesota, Missouri, Mississippi, Montana, North Dakota, Nebraska, New Mexico, Nevada, Oklahoma, Oregon, South Dakota, Tennessee, Texas, Utah, Washington and Wyoming.

The recalled products have both a “Guaranteed Fresh” date of 27 AUG 2019 and a nine-character manufacturing code that includes the numbers “29” in the second and third position (example: x29xxxxxx) listed below the “Guaranteed Fresh” date. These numbers can be found on the right side of the front of the bag. In addition, the recalled bags will also have a UPC code of “28400 63242” listed on the bottom left side of the back of the bag.

No other Lay’s or Lay’s Lightly Salted products or flavors are recalled.

The recall was initiated after it was discovered that bags of Lay’s Lightly Salted Barbecue Flavored Potato Chips were inadvertently filled with another flavor of potato chips, potentially exposing consumers to undeclared milk.

Consumers with the product noted above can return the product to a retailer for a refund or contact Frito- Lay Consumer Relations at 1-800-352-4477 (9 a.m. – 4:30 p.m. CST, Monday-Friday).

June 13, 2019 a repost from the Yeshiva World & confirmed by the Kof-K:

The Kof-K has been infomed that there is salmon being sold in Uruguay, South America as well as possibly in Latvia bearing an unauthorized Kof-K symbol. The Kof-K symbol is prominently displayed on the front of the packaging. The Kof-K is aggressively trying to trace the origin of this Salmon packer and currently finding extremely challenging to do so. We are applealing for the public's help in stopping this fraudulent activity.

If you see this product or any similar looking product, please call Rabbi Yehuda Rosenbaum, Kof-K administrative Director at 201-837-1967 IMMEDIATELY with the location of the product so further action can be taken.

In the meantime PLEASE HELP US get the word out by forwarding this alert to all of your contacts. Help us prevent anyone from mistakenly eating this productr that is not Kosher certified.

Kroger Recalls Select Frozen Private Selection Berries for Possible Health Risk

June 7, 2019 from the FDA

The Kroger Co. (NYSE: KR) said today it is recalling Private Selection Frozen Triple Berry Medley (48 oz), Private Selection Frozen Triple Berry Medley (16 oz), and Private Selection Frozen Blackberries (16 oz) manufactured by Townsend Farms due to possible Hepatitis A contamination.

No customer illnesses have been reported to date. Kroger was informed by the FDA that a sample of the Private Selection frozen berries was tested by the FDA and found to be contaminated with Hepatitis A.

Kroger is recalling the following items, which were distributed to all Kroger family of store bannersExternal Link Disclaimer across the country:

• PRIVATE SELECTION FROZEN TRIPLE BERRY MEDLEY, 48 OZ (BEST BY: 07-07-20; UPC: 0001111079120);
• PRIVATE SELECTION FROZEN TRIPLE BERRY MEDLEY, 16 OZ (BEST BY: 06-19-20; UPC: 0001111087808);
• PRIVATE SELECTION FROZEN BLACKBERRIES, 16 OZ (BEST BY: 06-19-20, 07-02-20; UPC: 0001111087809)

Kroger has removed the potentially affected items from store shelves and initiated its customer recall notification system that alerts customers who may have purchased recalled products through register receipt tape messages and phone calls. Customers who have purchased the above products should not consume them and should return them to a store for a full refund or replacement.

Customers who have questions may contact Kroger at 1-800-KROGERS Monday through Friday, 8:00 AM to midnight EST, and Saturday and Sunday, 8:00 AM to 9:30 PM EST.

June 5, 2019 from FARE:

Unilever is voluntarily recalling a limited number of boxes of Ben & Jerry’s Chocolate Fudge Brownie Pint Slices, which may inadvertently contain Vanilla Peanut Butter Cup Pint Slices. Although the slices were individually wrapped and identified as Vanilla Peanut Butter Cup Pint Slices, the ingredient peanut butter (containing the known allergen peanut), is undeclared on the outer product packaging.

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

The affected product is sold in a paperboard box, containing 9 fL oz (266 mL) (3 individually wrapped ice cream slices) with UPC code of 076840657940 best by dateAUG1218LT2 and lot number of AUG1218LT2.

The product was manufactured in the United States. The product was distributed nationwide and reached consumers through retail stores. No product was shipped outside of the U.S. No other Ben & Jerry’s products – besides this specific lot of Chocolate Fudge Brownie Pints Slices - are affected by this voluntary recall, including other Pint Slices, pints or any products served in Ben & Jerry's franchised Scoop Shops.

The recall was initiated after receiving one consumer complaint, where it was discovered that Vanilla Peanut Butter Cups Pint Slices were distributed in outer packaging that did not call out the presence of peanut butter. Unilever has not received any reports of illness associated with this product, but the company is voluntarily recalling this product out of an abundance of caution.

Consumers who have purchased boxes of the above product with the affected UPC code and date code are asked to immediately discontinue use of the product, retain the outer box and call 877-270-7397, which is operational 24 hours a day, for more information about the recall and to request a replacement coupon. A consumer services representative is available between the hours of 8:30 AM and 5:00 PM EDT.

Brodt Zenatti Holding LLC. Recalls Karawan Brand Tahini & SoCo Brand Tahini Because of Possible Health Risk

June 10, 2019 from the FDA

Brodt Zenatti Holding LLC of Jupiter, Florida is recalling all retail and bulk Karawan brand Tahini, sold in Jars: 450g (15.87 oz) and Buckets: 17kg (599.6 oz); 3kg (105.8 oz) that were imported from Palestine (ed note: their wording) between the dates of December 2018 to April 2019 and SoCo Brand Tahini; because they have the potential to be contaminated with Salmonella.

Karawan brand Tahini was directly distributed to New York and Texas. We currently know that distributors have thereafter shipped the product to Massachusetts and Virginia.
Specific information on how to identify the Karawan brand Tahini product includes:

1. Name of product: Tahini
2. Brand name: Karawan Tahini
3. Unit size: Jar: 450g (15.87 oz), Buckets: 17kg (599.6 oz), 3 kg (105.822 oz)
4. Storage conditions: No refrigeration storage needed.
5. Expiration Date (s): Two years from the production. The expiration date is located on the lid of the containers.

Retail label for SoCo brand Tahini
Specific information on how to identify the SoCo brand Tahini product includes:

Name of product: Tahini

Brand name: SoCo Tahini

Unit size: Container: 380g (13.4 oz)

Storage conditions: No refrigeration storage needed.

Expiration Date (s): Two years from the production. The expiration date is located on the lid of the containers.

This recall has been initiated due to New York City Department of Health and Mental Hygiene laboratory results from two samples of Karawan brand tahini testing positive for Salmonella. Brodt Zenatti Holding LLC has ceased the importation and distribution of the product as FDA and Brodt Zenatti Holding LLC continue their investigation as to what caused the problem.

Consumers who have purchased Karawan brand tahini or SoCo brand Tahini are urged to destroy it or return it to the place of purchase for a full refund. Consumers with questions may contact Brodt Zenatti Holding LLC at 305-570-9050, Monday through Friday, from 9:00 am to 5:00 pm.