Kodiak Premium Wintergreen Longcut Tobacco Tin
American Snuff Company (ASC) is voluntarily recalling certain lots of Kodiak Premium Wintergreen Longcut Tobacco manufactured at ASCs facility in Clarksville, TN, and distributed in Alabama, Florida, Georgia, Iowa, Illinois, Indiana, Kentucky, Michigan, Minnesota, North Carolina, New York, Ohio, Pennsylvania, South Carolina, Tennessee, Virginia, Wisconsin, and West Virginia. ASC has notified the U.S. Food and Drug Administration of the voluntary recall and is working with the Agency on this matter.
ASC initiated the recall of Kodiak Premium Wintergreen Longcut Tobacco after having identified the potential for certain lots of the product to contain foreign metal objects which may or may not be visible to the consumer. The recall was as the result of identifying an issue with manufacturing equipment during routine inspection that caused metal-to-metal abrasion; this abrasion could have caused metal shavings to come into contact with tobacco during the manufacturing process. To date, there have been no products identified as containing these foreign objects, no consumer complaints, or reports of consumer injury received. None of ASC's other products are affected, including its other styles of Kodiak, Grizzly, Hawken, and Cougar smokeless tobacco products, and all of its loose leaf, twist, dry snuff, and plug products.
ASC has instructed wholesalers and retailers to segregate the recalled Kodiak Premium Wintergreen Longcut Tobacco from their inventories. ASC's sales representatives are assisting wholesalers and retailers in returning the product.
A consumer who has any of the Kodiak Premium Wintergreen Longcut Tobacco product listed below should not open or use the product. Consumers should contact ASC at 1-866-843-0636 to return the product for a refund, report any adverse events, or submit a complaint.
The select cans subject to this recall have the following identifying information printed on the bottom of the cans.
The key characters to identify potentially affected product are in upper case and highlighted in red (See Image above). The x characters in lower case in the can code are not relevant to identifying potentially affected product.
GxxxxlK3 GxxBxJK3
GxxAxJK GxxCxJK3
If the characters in the Code printed on the bottom of the can match any of the Codes above, the product is considered potentially affected.
If the characters in the Code printed on the bottom of the can do NOT match the Codes above, this product is not affected.
Source and more images: FDA
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Consumers should contact ASC at 1-866-843-0636 to return the product for a refund, report any adverse events, or submit a complaint.
This link is being provided as a convenience and for informational purposes only it is not an endorsement or an approval of any of the products, services or opinions of the corporation or organization or individual.
Recallinsider.com bears no responsibility for the accuracy, legality or content of the external site or for that of subsequent links.
This link is being provided as a convenience and for informational purposes only it is not an endorsement or an approval of any of the products, services or opinions of the corporation or organization or individual.
Recallinsider.com bears no responsibility for the accuracy, legality or content of the external site or for that of subsequent links.
This link is being provided as a convenience and for informational purposes only it is not an endorsement or an approval of any of the products, services or opinions of the corporation or organization or individual.
Recallinsider.com bears no responsibility for the accuracy, legality or content of the external site or for that of subsequent links.
This link is being provided as a convenience and for informational purposes only it is not an endorsement or an approval of any of the products, services or opinions of the corporation or organization or individual.
Recallinsider.com bears no responsibility for the accuracy, legality or content of the external site or for that of subsequent links.