July 8, 2020 – KIND Healthy Snacks (KIND) is voluntarily recalling a limited number of Oats & Honey Granola with Toasted Coconut pouches due to the presence of sesame seeds, which is not listed as an ingredient in the product. The label does list “sesame seeds” under the “May Contain” statement.

People who have an allergy or sensitivity to sesame seeds should immediately discontinue use of this product.

KIND recently decided to transition away from using sesame seeds in its Oats & Honey Granola recipe. This limited recall was initiated after KIND discovered that the product’s previous recipe was used and placed into new packaging that did not disclose sesame seeds as an ingredient.

The recall applies to one flavor: KIND Oats & Honey Granola with Toasted Coconut. No other KIND products are affected by this recall.

The product is sold in a plastic pouch and is available in two sizes – 11 ounces (UPC: 60265217186-4) or 17 ounces (UPC: 60265225101-6).

The impacted product can be identified by looking for the Best By date, which is located on the bottom of the pouch:

• For the 11oz pouch, the Best By dates range from April 4, 2021 to June 1, 2021
• For the 17oz pouch, the Best By dates range from April 30, 2021 to June 1, 2021

Please visit kindsnacks.com/oatsandhoneygranolaExternal Link Disclaimer for more information.

Consumers who have purchased KIND Oats & Honey Granola that displays one of the abovementioned Best By Dates and can no longer consume the product safely due to an allergy or sensitivity to sesame seeds, should retain the packaging and email customerservice@kindsnacks.com.

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July 9, 2020- To be in compliance with FDA Drug Regulations, Sundial is requesting an immediate recall, removal and return, of all Sundial Products, distributed from the period beginning January 1, 2014 through current, that have labeling containing/making drug claims stating the product(s) can diagnose, cure, mitigate, treat or prevent disease. The recalled drug products are misbranded and deemed unapproved drugs based on labeling claims which could result in a delay of appropriate treatment by a healthcare provider. Because these products are unapproved, their safety and efficacy have not been established. While specific risks to patients, from use of these adulterated products, cannot always be identified or assessed, it is also not possible to rule out patient risks resulting from the use of such products.

The products included for recall are:

All products used as a Sundial Herbs can be identified by the “Sundial” label with brown glass bottles, boxes, Ziploc bags and paper bags with clear viewing windows. This was distributed state or nationwide via the Sundial Herb website (External Link Disclaimerhttp://sundialherbs.com/sundial/External Link Disclaimer)External Link Disclaimer, or any other website or store pick up at 3609 Boston Road, Bronx, New York. Please contact Sundial Herbs to schedule return orders for proper disposal and destruction of the products.

Consumers with further questions may contact Sundial Herbal Products via email atsundialherbalproducts@aol.com .

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June 13, 2020- 

Ridley Block Operations is voluntarily recalling Ultralyx® 12% Protein Sheep with batch number HB01679401. The product has been found to contain elevated levels of copper. With prolonged consumption, the affected product could potentially have adverse health effects on sheep, including reductions in daily gains, icterus, partially cirrhotic livers and hemoglobin-stained kidneys. Occasionally, death occurs in copper-toxic sheep.

This recall relates only to Ultralyx 12% Protein Sheep with the following batch numbers printed on the package:

Customers are asked to remove all product matching this batch number from distribution and inventory and discontinue feeding it immediately.

No other batch number or other Ridley Block Operations products are involved in this voluntary recall. Of the batch of twenty blocks included in the recall, two blocks remain in the marketplace.

Ridley Block Operations will continue to work closely with the Food and Drug Administration throughout the recall process. Our representatives are in direct communication with our customers to ensure the proper identification and removal of the impacted products.

For guidance on affected product inventory or any other questions, customers may contact Ridley Block Operations Customer Service at 1-606-849-2170 (Monday – Friday, 8:00 a.m. - 4:30 p.m. ET).

Customer Service: 1-606-849-2170
Media Contact: press@alltech.com

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