Missouriwatcher
Editor, Senior Moderator
December 20, 2010 - Bright Water Seafood, Tucker, GA is voluntarily recalling its 7 ounce packages of Buffalo Krab Dip and 7 ounce packages of Southwest Krab Dip because they have the potential to be contaminated with Listeria monocytogenes...
The recalled Dips & Spreads were distributed in retail stores in North Carolina, South Carolina, Tennessee, North Georgia and Virginia.
The Bright Water Buffalo Krab Dip product comes in a 7 ounce, clear plastic container marked with an UPC code 8 1971100001 4 and with an expiration date of 12/21/2010 stamped on the side. The Bright Water Southwest Krab Dip comes in a 7 ounce, clear plastic container marked with an UPC code 8 1971100002 1 and with an expiration date of 12/29/2010 stamped on the side.
No illnesses have been reported to date in connection with this problem.
The potential for contamination was noted after routine testing by the company revealed the presence of Listeria monocytogenes in 7 ounce container.
The production of the product has been suspended while the Company, GA Department of Agriculture and US FDA continue to investigate the source of the problem.
http://www.fda.gov/Safety/Recalls/ucm237791.htm
The recalled Dips & Spreads were distributed in retail stores in North Carolina, South Carolina, Tennessee, North Georgia and Virginia.
The Bright Water Buffalo Krab Dip product comes in a 7 ounce, clear plastic container marked with an UPC code 8 1971100001 4 and with an expiration date of 12/21/2010 stamped on the side. The Bright Water Southwest Krab Dip comes in a 7 ounce, clear plastic container marked with an UPC code 8 1971100002 1 and with an expiration date of 12/29/2010 stamped on the side.
No illnesses have been reported to date in connection with this problem.
The potential for contamination was noted after routine testing by the company revealed the presence of Listeria monocytogenes in 7 ounce container.
The production of the product has been suspended while the Company, GA Department of Agriculture and US FDA continue to investigate the source of the problem.
http://www.fda.gov/Safety/Recalls/ucm237791.htm