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Soy Allergy Alert

1 post in this topic




September 27, 2006

Snack Alliance, Inc. is recalling nacho flavored tortilla chips due to

undeclared soy.

Packages of Nacho flavored tortilla chips having a best by date prior to

and including FEBRUARY 7, 2007. The date which can be found in the upper

right hand corner of packages. They were sold in retail stores under the

following brands:

*Laura Lynn Nacho Flavored Tortilla Chips, 13-ounce package distributed in

the Southeastern US

*Southern Home Nacho Flavored Tortilla Chips, 13-ounce package distributed

in the Southeastern US

*Filler Brand Nacho Flavored Tortilla Chips, 1, 1.5, and 9-ounce packages

distributed in Puerto Rico

*Kid Connection Nacho Flavored Tortilla chips as a component in Kid

Connection variety snack sacks, 1 -ounce packages with Julian code dates

of 17706 to 19106 distributed nationally by WAL-MART

*Food Lion Nacho Flavored Tortilla Chips as a component in Food Lion

variety snack sacks, 1-ounce packages distributed in the Eastern US

*Food Express Cantina Style Nacho Tortilla Chips, 16-ounce packages

distributed in Ohio

Consumers may return the product to the place of purchase for a full

refund. Consumers with questions may contact the company at (800) 665-



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    • Those could be celiac symptoms or they could be something else.  Just because celiac runs in your family, I would not jump to conclusions.  That could be dangerous!   For example, my niece presented with celiac disease symptoms.  She tested negative but they found that she has Crohn's (not that she can't ever develop celiac disease).  While a gluten free diet could not hurt her, it is not the cause of her Crohn's flare-ups.    I would not worry about his weight unless he is no longer on the growth charts.   There could be more related to his anxiety issues too. i would NOT recommend sharing prescriptions, especially on a 9 year old!  Dapsone is some pretty evil medication that can do some serious liver damage (but if you have DH or  leporisy, it might be worth the risk -- but I would think not for kids).  For DH, sticking to a gluten-free diet  is much preferred, but I will let one of our members who has DH comment on that.   Those with DH often do not test positive in blood work.  Best to get a skin biopsy (tricky on DH so read up). Please find a dermatologist  and/or a Ped GI who is celiac savvy.    
    • Canadian Celiac Association warns against Gluten-Free Cheerios, but is there good evidence? View the full article
    • So, now they have found a metal toxicity in my body along with needing to be gluten free.  For the toxicity, I am now taking supplements after and between meals.  This a good thing because it prompts me to actually eat 3 meals a day and in a timely manner and not just a grab on the go item whenever.  The down side is remembering to take the silly things.  I can honestly say how much a pain it is to remember to take the supplements sometimes.  Been on this regimen for about a week now, and I am starting to feel better and all my systems are getting thoroughly cleaned out.  The real test will be in about 3 weeks or so, as it is about this time I become more vulnerable to the neurological symptoms.  I actually did some research on metal toxicity and found something incredible.  The symptoms I had been having all fall under this problem.  This could also have been yet another contributing factor of why I needed to go gluten free. Just a thought.  One thing I did consistently find is that once the toxicity is taken care of, this would not take away any food allergies or gluten issues.  I had gone through a different detox program back in February-March, and the neurological symptoms I have been dealing with was magnified x10 it seemed.  Another praise in this regimen is that I have been virtually symptom free since taking these supplements.  A few episodes but very minor.   
    • I have not taken him to a dermatologist. I have dapsone, which I put on the rash, it always clears up. I have it for another family member. But then I started reading about celiac and all these dots are out there but not connected.  The next time he has the bumps, I am going to take him in. In the mean time, I am trying to find a dermatologist who understands the condition. I don't want my kid to have celiac. And I kinda feel crazy for thinking he may have a gluten issue but with it in my family and him having these other things, I want to be dilligent.   i will read up on the test you suggested. Thanks for taking the time to read and respond everyone.   
    • I tested positive to deamidated gliadin in August at a hospital. My old GI tested me using gliadin (the test listed on your result) in September and it was negative. Literally the next day, my new GI tested for deamidated gliadin again and it was positive (I was unaware the hospital scheduled an appointment with the new GI for follow up).  If you still suspect it, Google deamidated gliadin, print out the Mayo clinic lab info and circle the part where it says they have discontinued the use of gliadin in favor of the deamidated gliadin.  Has he seen a dermatologist?
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