Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

Tyson Chicken Breast


bakinghomesteader

Recommended Posts

bakinghomesteader Contributor

Is their boneless, skinless chicken breast gluten free? I see they have added broth.


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



bakinghomesteader Contributor

No one knows? I emailed them, but no answer. I just thought someone would know.

GlutenGalAZ Enthusiast

I got a bag of the frozen chicken you are talking about at WalMart... I have had it a couple of times and haven't noticed any problems. I was going to call them about the broth in it but forgot before I left for work.

There should be a toll free line on the bag you can call.

GlutenGalAZ Enthusiast
Is their boneless, skinless chicken breast gluten free? I see they have added broth.

I just called really quick and asked -- did't get into detail though about what type of broth (ahh forgot, I am on lunch right now at work). The rep at the contact phone number said that the broth is gluten free and so is that chicken.

happygirl Collaborator

All plain meats/chicken/etc are gluten free. By law, any grain must be listed on meat products.

Its gluten free.

bakinghomesteader Contributor

Thanks all. It just said chicken broth and not what was in the broth. So I just wondered. Thanks again.

bakinghomesteader Contributor

I never did get an email, but I DID get a letter in the mail. :D It said the chicken broth was gluten free and they sent me coupons. :P Yeah!


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



  • 2 months later...
Algdoll Newbie
I never did get an email, but I DID get a letter in the mail. :D It said the chicken broth was gluten free and they sent me coupons. :P Yeah!

Thanks so much for doing the leg work on this for me! I usually buy the Great Value brand at Walmart, but they were out and I bought the Tyson brand. Forgot to check on gluten-free status until just now when I'm about to throw it in the oven. Thanks so much!

  • 2 years later...
quincy1775 Newbie

I'm not sure if they have gluten or not, but I do know that I always react to Tyson chicken, along with Holly Farms, Great Value, and Kroger brands, all of which say they contain a broth solution. The reaction is just like a gluten reaction, maybe even a tad more violent than if I simply ate a loaf of bread. But it's bad.

I've since switched to other brands of chicken like Perdue (they provide a gluten-free list on their website), some Food Lion frozen chicken (that uses only a salt/water solution), Harvestland, and locally-raised options...and I never react to them.

I did a test to confirm my suspicions, and isolated it to the chicken after having continued gluten-like reactions to simple dishes like chicken and rice. When I switched chicken suppliers, the reactions went away and have been gone for more than 8 months.

Not sure why that would be, but I avoid Tyson products now as a result to be on the safe side. I don't even have chicken in a restaurant unless I can verify its source, it's too risky and I react too horribly to it to take the chance.

lovegrov Collaborator

"I always react to Tyson chicken, along with Holly Farms, Great Value, and Kroger brands,"

I've used all of those brands except GV and they are gluten-free.

richard

  • 2 years later...
texasarah Newbie

Hi All,

I know I'm arriving late to this conversation but I found this thread today as I was doing a bit of research (somehow I just realized that the boneless skinless chicken breasts I've been purchasing for 3 years may have had gluten in them - yikes!). Anyway, I did a search on the Tyson website and found this information:

http://www.tyson.com...en-Chicken.aspx

It specifically states,

"INGREDIENTS:

Boneless, skinless chicken breasts with rib meat contains up to 15% natural chicken broth. ALL NATURAL CHICKEN BROTH INGREDIENTS: Chicken broth, salt, natural flavorings.

CONTAINS NO ALLERGENS"

This may be old news to everyone else, but it was helpful/reassuring for me :)

  • 2 years later...
snow4jc Newbie
On 2/18/2013 at 1:44 PM, texasarah said:

 

I'm also responding late to this thread, but when I read this last response I had to comment.  I'm not celiac, but have a multitude of food intolerance, which cause extreme inflammation in my whole body and many physical repercussions.  I'm Always finding something else that titles up my body even when I thought I was eating safely.  

Please be aware that natural flavoring is something you should avoid.  It is listed on ingredient lists, but they don't tell you what is in it!  I have too avoid it like the plague, along with caramel coloring.  They both very often include a wheat derivative.  

I just ate two different kilter products, a fresh Turkey for thanksgiving and a Tyson whole chicken yesterday.  I have reacted to both. ??.  The solution is the culprit.  There was no other foods that were suspect because they were freshly prepared veggies and sweet potatoes which don't bother me.

This is so frustrating....    There are many other additives and preservatives that also affect me.  So I eat fresh only... Make all my own food.  

Hope this helps someone who still reacts when they think they're eating cleanly but react.

On 2/18/2013 at 1:44 PM, texasarah said:

"INGREDIENTS:

Boneless, skinless chicken breasts with rib meat contains up to 15% natural chicken broth. ALL NATURAL CHICKEN BROTH INGREDIENTS: Chicken broth, salt, natural flavorings.

 

CONTAINS NO ALLERGENS"

 

This may be old news to everyone else, but it was helpful/reassuring for me :)

 

squirmingitch Veteran
3 hours ago, snow4jc said:

Please be aware that natural flavoring is something you should avoid.  It is listed on ingredient lists, but they don't tell you what is in it!  I have too avoid it like the plague, along with caramel coloring.  They both very often include a wheat derivative.  

I just ate two different kilter products, a fresh Turkey for thanksgiving and a Tyson whole chicken yesterday.  I have reacted to both. ??.  The solution is the culprit.  There was no other foods that were suspect because they were freshly prepared veggies and sweet potatoes which don't bother me.

This is so frustrating....    There are many other additives and preservatives that also affect me.  So I eat fresh only... Make all my own food.  

Hope this helps someone who still reacts when they think they're eating cleanly but react.

 

Please do not spread rumors like this on the board. These 2 items are a huge misconception. Please read the following links:

http://www.glutenfreedietitian.com/flavorings-extracts-are-they-gluten-free/

http://www.delightglutenfree.com/glutenfreemyths#.Vm8UoRGG-Ww

If natural flavors and carmel coloring were glutening celiacs then most of us would be dead by now. 

cyclinglady Grand Master

Squirming itch is right.  I drank a Diet Coke on Saturday during a party and I did not get glutened.  It was full of Carmel coloring.  There was not any safe party food for me.  Diet Coke is not healthy, but at least I looked like I was indulging in something!  

  • 3 years later...
Valkyrie Newbie
(edited)

quincy1775 and snow4jc make a good point.

I usually get sick from these products, too. What doesn't make some people sick, will make others sick. There isn't one "way" to be a celiac or allergic to wheat. Sometimes natural flavorings and carmel do contain wheat, according to the links squirmingitch provided and other sources. But sometimes they do not. Just like soy sauce. Just like cross-contaminated chicken breast or breast from chicken fed a wheat diet. Just like products labeled gluten-free that are processed in a facility that also processes wheat. Sometimes they make people sick, sometimes they do not.

It's not a rumor because it happens to people who are celiac often enough. Not everyone experiences the world the way you do, squirmingitch. You're very fortunate yourself that those products don't make you ill, personally. 

As for me and it seems quincy and snow, we must avoid those products because they have potential to be cross contaminated with, or derived from, wheat. It's a harmful misconception you spread, squirmingitch, when you tell other celiacs that their experience is invalid. Shaming people who are in tune with their body is extremely unskillful.

Isn't it helpful for celiacs like me and snow to know to avoid these products, too?

Edited by Valkyrie
additional information

Create an account or sign in to comment

You need to be a member in order to leave a comment

Create an account

Sign up for a new account in our community. It's easy!

Register a new account

Sign in

Already have an account? Sign in here.

Sign In Now

  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      127,912
    • Most Online (within 30 mins)
      7,748

    kels0831
    Newest Member
    kels0831
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121k
    • Total Posts
      70.5k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Jack Common
      Hello! I want to share my situation. I had symptoms like some food intolerance, diarrhea, bloating, belching one year ago. I thought I could have celiac disease so I did the blood tests. The results were ambiguous for me so I saw the doctor and he said I needed to do tests to check whether I had any parasites as well. It turned out I had giardiasis. After treating it my symptoms didn't disappear immediately. And I decided to start a gluten free diet despite my doctor said I didn't have it. After some time symptoms disappeared but that time it wasn't unclear whether I'd had them because of eliminating gluten or that parasite. The symptoms for both are very similar. Giardiasis also damages the small intestine. The only way to check this was to start eating bread again as I thought. Now about my results.   These are my first test results (almost a year ago) when I had symptoms: The Tissue Transglutaminase IgA antibody - 0.5 U/ml (for the lab I did the tests 0.0 - 3.0 is normal) The Tissue Transglutaminase IgG antibody - 6.6 U/ml (for the lab I did the tests 0.0 - 3.0 is normal) Immunoglobulin A - 1.91 g/l (for the lab I did the tests 0.7 to 4 g/l is normal) IgA Endomysial antibody (EMA) - < 1:10 titer (for the lab I did the tests < 1:10 titer is normal) IgG Endomysial antibody (EMA) - < 1:10 titer (for the lab I did the tests < 1:10 titer is normal) Deamidated gliadin peptide IgA - 0.3 U/ml (for the lab I did the tests 0.0 - 6.0 is normal) Deamidated gliadin peptide IgG - 46.1 U/ml (for the lab I did the tests 0.0 - 6.0 is normal)   Then I didn't eat gluten for six months. Symptoms disappeared. And I started a gluten challenge. Before the challenge I did some tests. My results: The Tissue Transglutaminase IgG antibody - 0.5 U/ml (for the lab I did the tests < 20 U/ml is normal)) Deamidated gliadin peptide IgG - 28 U/ml (for the lab I did the tests < 20 U/ml is normal)   During the challenge I ate 6 slices of wheat bread. After the challenge my results are: The Tissue Transglutaminase IgA antibody - 2.0 U/ml (for the lab I did the tests < 20 U/ml is normal) The Tissue Transglutaminase IgG antibody - 2.0 U/ml (for the lab I did the tests < 20 U/ml is normal) Immunoglobulin A - 1.31 g/l (for the lab I did the tests 0.7 to 4 g/l is normal) Deamidated gliadin peptide IgA - 2.0 U/ml (for the lab I did the tests < 20 U/ml is normal) Deamidated gliadin peptide IgG - 2.13 U/ml (for the lab I did the tests < 20 U/ml is normal)   To be sure I continued consuming gluten. I ate a lot each day. Two months after I did the tests again. My results I got today are: The Tissue Transglutaminase IgA antibody - 0.7 U/ml (for the lab I did the tests < 20 U/ml is normal) Immunoglobulin A - 1.62 g/l (for the lab I did the tests 0.7 to 4 g/l is normal) Deamidated gliadin peptide IgG - 25.6 U/ml (for the lab I did the tests < 20 U/ml is normal)   Nowadays I didn't have any symptoms except tiredness but I think it's just work. I think it was this parasite because two years ago, for example, and before I didn't have these symptoms and I always ate gluten food. But I'm still not sure especially because the Deamidated gliadin peptide IgG results are sometimes high. What do you think? @Scott Adams
    • Jack Common
      My old results (almost a year ago) are: The Tissue Transglutaminase IgA antibody - 0.5 U/ml (for the lab I did the tests 0.0 - 3.0 is normal) The Tissue Transglutaminase IgG antibody - 6.6 U/ml (for the lab I did the tests 0.0 - 3.0 is normal) Immunoglobulin A - 1.91 g/l (for the lab I did the tests 0.7 to 4 g/l is normal) IgA Endomysial antibody (EMA) - < 1:10 titer (for the lab I did the tests < 1:10 titer is normal) IgG Endomysial antibody (EMA) - < 1:10 titer (for the lab I did the tests < 1:10 titer is normal) Deamidated gliadin peptide IgA - 0.3 U/ml (for the lab I did the tests 0.0 - 6.0 is normal) Deamidated gliadin peptide IgG - 46.1 U/ml (for the lab I did the tests 0.0 - 6.0 is normal)   Then I didn't eat gluten for six months and after I started a gluten challenge. Before the challenge I did some tests. My results: The Tissue Transglutaminase IgG antibody - 0.5 U/ml (for the lab I did the tests < 20 U/ml is normal)) Deamidated gliadin peptide IgG - 28 U/ml (for the lab I did the tests < 20 U/ml is normal)   During the challenge I ate 6 slices of wheat bread. After the challenge my results are: The Tissue Transglutaminase IgA antibody - 2.0 U/ml (for the lab I did the tests < 20 U/ml is normal) The Tissue Transglutaminase IgG antibody - 2.0 U/ml (for the lab I did the tests < 20 U/ml is normal) Immunoglobulin A - 1.31 g/l (for the lab I did the tests 0.7 to 4 g/l is normal) Deamidated gliadin peptide IgA - 2.0 U/ml (for the lab I did the tests < 20 U/ml is normal) Deamidated gliadin peptide IgG - 2.13 U/ml (for the lab I did the tests < 20 U/ml is normal)   To be sure I continued consuming gluten. I ate a lot each day. Two months after I did the tests again. My results I got today are: The Tissue Transglutaminase IgA antibody - 0.7 U/ml (for the lab I did the tests < 20 U/ml is normal) Immunoglobulin A - 1.62 g/l (for the lab I did the tests 0.7 to 4 g/l is normal) Deamidated gliadin peptide IgG - 25.6 U/ml (for the lab I did the tests < 20 U/ml is normal)   I didn't have any symptoms now except tiredness but I think it's just work. I'm not IgA deficient as you can see so I don't need to do this Deamidated gliadin peptide IgG test. But I do because it's sometimes not in the normal range. What do you think this time? I think I don't have celiac disease. But this test... 
    • Wheatwacked
      @plumbago, I found a good PDF on cholesterol:  Unlocking the mysteries of VLDL: exploring its production, intracellular trafficking, and metabolism as therapeutic targets I just started it, but it may have answers for us, with whacky cholesterol.  The pharmaceuticals don't seem to be interested in anything but statins.   "The nicotine in tobacco causes a decrease in the HDL cholesterol level. " Maybe you should start smoking? 🤪 I have high LDL and low HDL.  It is genetic mutations in the LDLR, APOB, PCSK9, or LDLRAP1 genes. My whole family is on statins for Familial Hyperliperdemia except me.  December I had ultrasound and cat scan for Carotid Artery blockage and both sides are above 85% blockage.  I started on Atorvastatin and that made me weaker than ever, even with CoQ10.  I asked for and got prescription for 2000 mg/day Nicotinic Acid B3 and in the 3 weeks my numbers changed. I am feeling realy good lately.  Stronger and more flexible.  Sleeping better.  Getting roto router (TCar) as soon as I get clearance from a cardiologist.  I expect that by my next blood panels in April to be even better. I am beginning to believe that like vitamin D where the RDA only accounts for preventing Rickets, the RDA for B3 is way underestimated.   From Oct 22 to Jan 17: A1c from 13.5 to 10.2 eGFR from 55 to 79 Triglyeride from 458 to 362 Total cholesterol from 245 to 264 HDL from 27 to 44 VLDL from 84 to 68 LDL from 134 to 154
    • plumbago
      I have taken thiamine on and off (just not at this exact moment), and I’m not sure it's made any difference. Yes, I almost always “fast” (12 hours NPO) for blood tests, as do a great many other Americans, so I tend to think that’s not it. All I can say is that the mystery continues. I could do some speculating here…well, heck, let me go ahead and speculate now: The lab ranges we all see on our reports are more or less the averages of Americans who have had those blood tests. Now, it’s up to you and me whether or not to think of the average American as healthy. I can make arguments both ways, more often than not, on the negative. My point here is that maybe the current range of HDL is somewhat skewed (ie, low), and maybe just maybe my super high (plus 100s) HDL results are not something to worry about; the range just needs updating. Why do I say this? Because pre-celiac disease diagnosis, my HDL values were in the normal range, but post celiac disease diagnosis, my HDL levels are way above average. See where I’m going? My trusty guidebook on celiac disease, Recognizing Celiac Disease by Cleo Libonati, RN, BSN, says that HDL increases after being on the gluten free diet. Or can increase, I guess. Then again, it could be something else. ¯\_(ツ)_/¯ In thinking of going to a cardiologist, I sort of fear that he/she will be dismissive of a link to celiac disease, treated celiac disease, and would not therefore be considering all possibilities. @trents I'm sorry you've been diligently working on your numbers to no effect. That must be frustrating. LDL is a world that is far better understood than HDL, so for you there's maybe less "mystery." Familial hypercholesterolemia is for sure something that can be tested. Outside of that, you're right, genetics can determine a general pattern.
    • trents
      Well, I have the opposite problem. My LDL has been moderately high for years. I eat healthy and exercise regularly but can't seem to move that meter. I used to be on a statin (and my doctors want me to go back on one) and it brought both HDL and LDL down but the ratios never changed. I think a lot of that cholesterol stuff is just baked into the genes.
×
×
  • Create New...