Jump to content
  • 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

Trader Joe's- Unofficial Poll


confusedks

Recommended Posts

confusedks Enthusiast

I just am curious to hear who reacts to Trader Joe's products? A lot of their products are gluten free, but they are made on equipment shared with wheat. I just want to who eats these products specifically from Trader Joe's. I bought their pumpkin butter which is amazing, but I think I am reacting to it because it's made in a facility that processes....

Thank you!

Kassandra


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



Celiac.com Sponsor (A8-M):



tarnalberry Community Regular

while I haven't had a lot of problem with their stuff, I don't have it all that often.

the good news, on that product, is that pumpkin butter is super easy to make from scratch - well, super easy from canned pumpkin, and just easy from a whole pie pumpkin, so if you still want it, you can just make your own.

DingoGirl Enthusiast

Trader Joe's is about two miles from my house and I can't imagine life without it! I am there about twice a week (am on a hugging basis w/ one of the employees and quite a chatting basis with a couple of others :)) and eat TONS of stuff there, no problems at all!

If you like, I"ll write the long list for you....but many of the things, I think, are made on shared equipment, but I haven't reacted at all.

confusedks Enthusiast

Thank you. I am not sure if I react to their stuff. I think it might be the sugar content in the pumpkin butter. We also live at TJ's. I don't know what we'd do without them either. They know us too! LOL!

Kassandra

dadoffiveboys Rookie
Thank you. I am not sure if I react to their stuff. I think it might be the sugar content in the pumpkin butter. We also live at TJ's. I don't know what we'd do without them either. They know us too! LOL!

Kassandra

I'm going to guess it depends on the particular 'trader joes' and also how they make each product. I know I had a gluten-free flourless chocolate cake.. and myself and two of my sons reacted to it (cross-contaminated). Two of my other sons did not react nor my father. We are also sensitive to gluten but the ones that reacted .. we are VERY sensitive.

If you are highly sensitive I wouldn't recommend any product produced on shared equipment for sure and would rule out Trader Joes products.

Another thing.. my dad said he had 'no reaction' but when he originally went completely gluten-free he was off his blood pressure medicine.. he is now back on it (lower dose) and he eats gluten-free when he goes out, etc.. but I believe he would be off his medicine COMPLETELY if he were 100% gluten-free... I think you get used to the cross contamination. I eat only food I prepare at home so that may explain why I have such a high reaction to even the smallest amounts. My children are homeschooled and also do not get gluten. (We are EXTREMELY healthy now and don't get sick either!!!)

Just my 2 cents..

mandasmom Rookie
I'm going to guess it depends on the particular 'trader joes' and also how they make each product. I know I had a gluten-free flourless chocolate cake.. and myself and two of my sons reacted to it (cross-contaminated). Two of my other sons did not react nor my father. We are also sensitive to gluten but the ones that reacted .. we are VERY sensitive.

If you are highly sensitive I wouldn't recommend any product produced on shared equipment for sure and would rule out Trader Joes products.

Another thing.. my dad said he had 'no reaction' but when he originally went completely gluten-free he was off his blood pressure medicine.. he is now back on it (lower dose) and he eats gluten-free when he goes out, etc.. but I believe he would be off his medicine COMPLETELY if he were 100% gluten-free... I think you get used to the cross contamination. I eat only food I prepare at home so that may explain why I have such a high reaction to even the smallest amounts. My children are homeschooled and also do not get gluten. (We are EXTREMELY healthy now and don't get sick either!!!)

Just my 2 cents..

We eat TJs stuff all the time....much of it is prepared on shared equipment...I suppose the only way to know for sure is to periodically have blood drawn to tell if you are reating to the small possiblity of CC. Even shared equipment must be thoroughly cleaned between products..that insures the taste and quality of the food. We havent had any overt problems with anything we have purchased there...so I suppose its a risk we are willing to take!!!

cruelshoes Enthusiast

We eat so much TJ's food it isn't funy. We don't react to any of the products we have tried (LOTS of them :huh: ), and our antibodies are negative. The thing about Trader Joe's is that they don't produce a lot of their products. They have other companies produce them, and then put the TJ's label on them. Last I heard, their pasta was made by tinkyada, for example. So it would be hard to generalize about reacting to their products, since they are made by so many different companies in so many different places.

My only beef with TJ's is that their gluten-free list has errors on it. I always tell people to use it as a starting place, but not to trust it too far. You still have to check the label every time you buy something.


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



Celiac.com Sponsor (A8-M):



saaa-wheat<3 Apprentice
We eat so much TJ's food it isn't funy. We don't react to any of the products we have tried (LOTS of them :huh: ), and our antibodies are negative. The thing about Trader Joe's is that they don't produce a lot of their products. They have other companies produce them, and then put the TJ's label on them. Last I heard, their pasta was made by tinkyada, for example. So it would be hard to generalize about reacting to their products, since they are made by so many different companies in so many different places.

My only beef with TJ's is that their gluten-free list has errors on it. I always tell people to use it as a starting place, but not to trust it too far. You still have to check the label every time you buy something.

I've never had a problem, though I don't eat much from there either. My favorite are the Savory Sesame Rice thin crackers...yum...they are about an hour away from me, otherwise, I'd be getting more from them!

I didn't know that their pasta is made by Tinkyada! Yay!! I'll have to get some on the next run. Maybe it will be the same price as when I find it at the discount food store :rolleyes:

Juliebove Rising Star

I don't buy anything that was made on shared lines. But then we have numerous allergies. It's not just gluten.

hathor Contributor

I reacted to TJ nuts once, so I won't go there again. I haven't noticed a reaction to anything else, but I'm always nervous when I see those warnings. I guess I just go with a TJ item when I can't find a sub.

Like a locally available dark chocolate bar made without soy lecithin :rolleyes:

Unfortunately, those warning labels are voluntary. Companies decide for themselves whether to have them. (The only restriction I think is that the labels have to be accurate.) So just because one gets something somewhere else that lacks a warning label doesn't mean that it is not manufactured on shared equipment.

The only labelling legally required is for the 8 allergens, with wheat being one (and not gluten, unfortunately). The requirement is for labelling of intentional ingredients. Cross-contamination or unintentional contents don't have to be shown.

Guest j_mommy

No problems with any of their stuff!

Susanna Newbie

I eat Trader Joe's stuff all the time and have never had a problem I could feel on my insides. But, even more objective data is that I just had my annual celiac serologies (blood tests) checked, and everything came back negative, so I say Trader Joes is safe for me. And I sure appreciate how much cheaper their stuff is than Whole Foods' and Sprouts' is.

Susanna

babinsky Apprentice

I am a new celiac and went to TJ's last night...I only found a couple of things that are gluten-free...is there a list of things I should know to look for?

Mango04 Enthusiast
I am a new celiac and went to TJ's last night...I only found a couple of things that are gluten-free...is there a list of things I should know to look for?

Open Original Shared Link a list. They're always getting new products, so don't assume that just because something's not on the list, it's not safe.

They sell great gluten-free ginger snaps and gluten-free granola. I've heard good things about the gluten-free pancakes too.

Mango04 Enthusiast

Oh - and I don't react to their products :)

DingoGirl Enthusiast
Open Original Shared Link a list. They're always getting new products, so don't assume that just because something's not on the list, it's not safe.

They sell great gluten-free ginger snaps and gluten-free granola. I've heard good things about the gluten-free pancakes too.

OMG I love love LOVE the frozen pancakes!!! Toast in toaster oven to perfection and put a little bit of butter in pure maple syrup, heat that in the microwave - YUM!!!

I also love the gluten-free granola. It's pricey, though......

Mango04 Enthusiast
I also love the gluten-free granola. It's pricey, though......

I know huh...what's the deal with the billion dollar granola...very unTrader Joe-like. It's pretty much just sugary corn too :rolleyes: Yummy though. I buy it and eat it often :rolleyes:

elonwy Enthusiast

I have reacted to a couple of TJ's things that were made on shared lines (a guac mix and something else). I now avoid anything from Tj's that says shared lines. I am very sensitive, and I am also a bit more careful than many that I know, because when I get sick it takes a long time for me to get better. I used to be a bit more blase about the shared lines thing, but now I'm getting pretty militant about not buying anything that states its made on a shared line.

babinsky Apprentice

Mango04....

Thank you soooo much for this list....my next shopping trip will be so much easier!

Nutmegger Rookie

I really like Trader Joe's and haven't had any issues myself. My only gripe is that they actually have a /lot/ of gluten-free products that simply aren't marked as gluten-free on the packages -- unless, of course, you read the ingredients. Hopefully, their new labelling system will deal with that. It will make shopping so much easier!

Archived

This topic is now archived and is closed to further replies.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,137
    • Most Online (within 30 mins)
      7,748

    Jamy
    Newest Member
    Jamy
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Sarah Grace
      Dear Kitty Since March I have been following your recommendations regarding vitamins to assist with various issues that I have been experiencing.  To recap, I am aged 68 and was late diagnosed with Celiac about 12 years ago.  I had been experiencing terrible early morning headaches which I had self diagnosed as hypoglycaemia.  I also mentioned that I had issues with insomnia, vertigo and brain fog.   It's now one year since I started on the Benfotiamine 600 mg/day.  I am still experiencing the hypoglycaemia and it's not really possible to say for sure whether the Benfotiamine is helpful.  In March this year, I added B-Complex Thiamine Hydrochloride and Magnesium L-Threonate on a daily basis, and I am now confident to report that the insomnia and vertigo and brain fog have all improved!!  So, very many thanks for your very helpful advice. I am now less confident that the early morning headaches are caused by hypoglycaemia, as even foods with a zero a GI rating (cheese, nuts, etc) can cause really server headaches, which sometimes require migraine medication in order to get rid off.  If you are able to suggest any other treatment I would definitely give it a try, as these headaches are a terrible burden.  Doctors in the UK have very limited knowledge concerning dietary issues, and I do not know how to get reliable advice from them. Best regards,
    • knitty kitty
      @rei.b,  I understand how frustrating starting a new way of eating can be.  I tried all sorts of gluten-free processed foods and just kept feeling worse.  My health didn't improve until I started the low histamine AIP diet.  It makes a big difference.   Gluten fits into opioid receptors in our bodies.  So, removing gluten can cause withdrawal symptoms and reveals the underlying discomfort.  SIBO can cause digestive symptoms.  SIBO can prevent vitamins from being absorbed by the intestines.  Thiamine insufficiency causes Gastrointestinal Beriberi (bloating, abdominal pain, nausea, diarrhea or constipation).  Thiamine is the B vitamin that runs out first because it can only be stored for two weeks.  We need more thiamine when we're sick or under emotional stress.  Gastric Beriberi is under recognised by doctors.  An Erythrocyte Transketolace Activity test is more accurate than a blood test for thiamine deficiency, but the best way to see if you're low in thiamine is to take it and look for health improvement.  Don't take Thiamine Mononitrate because the body can't utilize it well.  Try Benfotiamine.  Thiamine is water soluble, nontoxic and safe even at high doses.  I thought it was crazy, too, but simple vitamins and minerals are important.  The eight B vitamins work together, so a B Complex, Benfotiamine,  magnesium and Vitamin D really helped get my body to start healing, along with the AIP diet.  Once you heal, you add foods back in, so the AIP diet is worth doing for a few months. I do hope you'll consider the AIP diet and Benfotiamine.
    • captaincrab55
      Imemsm, Most of us have experienced discontinued, not currently available or products that suddenly become seasonal.   My biggest fear about relocating from Maryland to Florida 5 years ago, was being able to find gluten-free foods that fit my restricted diet.  I soon found out that the Win Dixie and Publix supper markets actually has 99% of their gluten-free foods tagged, next to the price.  The gluten-free tags opened up a  lot of foods that aren't actually marked gluten-free by the manufacture.  Now I only need to check for my other dietary restrictions.  Where my son lives in New Hartford, New York there's a Hannaford Supermarket that also has a gluten-free tag next to the price tag.  Hopefully you can locate a Supermarket within a reasonable travel distance that you can learn what foods to check out at a Supermarket close to you.  I have dermatitis herpetiformis too and I'm very sensitive to gluten and the three stores I named were very gluten-free friendly.  Good Luck 
    • rei.b
      Okay well the info about TTG-A actually makes a lot of sense and I wish the PA had explained that to me. But yes, I would assume I would have intestinal damage from eating a lot of gluten for 32 years while having all these symptoms. As far as avoiding gluten foods - I was definitely not doing that. Bread, pasta, quesadillas (with flour tortillas) and crackers are my 4 favorite foods and I ate at least one of those things multiple times a day e.g. breakfast with eggs and toast, a cheese quesadilla for lunch, and pasta for dinner, and crackers and cheese as a before bed snack. I'm not even kidding.  I'm not really big on sugar, so I don't really do sweets. I don't have any of those conditions.  I am not sure if I have the genes or not. When the geneticist did my genetic testing for EDS this year, I didn't think to ask for him to request the celiac genes so they didn't test for them, unfortunately.  I guess another expectation I had is  that if gluten was the issue, the gluten-free diet would make me feel better, and I'm 3 months in and that hasn't been the case. I am being very careful and reading every label because I didn't want to screw this up and have to do gluten-free for longer than necessary if I end up not having celiac. I'm literally checking everything, even tea and anything else prepacked like caramel dip. Honestly its making me anxious 😅
    • knitty kitty
      So you're saying that you think you should have severe intestinal damage since you've had the symptoms so long?   DGP IgG antibodies are produced in response to a partial gluten molecule.  This is different than what tissue transglutaminase antibodies are  produced in response to.   TTg IgA antibodies are produced in the intestines in response to gluten.  The tTg IgA antibodies attack our own cells because a structural component in our cell membranes resembles a part of gluten.  There's a correlation between the level of intestinal damage with the level of tTg antibodies produced.  You are not producing a high number of tTg IgA antibodies, so your level of tissue damage in your intestines is not very bad.  Be thankful.   There may be reasons why you are not producing a high quantity of tTg IgA antibodies.  Consuming ten grams or more of gluten a day for two weeks to two months before blood tests are done is required to get sufficient antibody production and damage to the intestines.  Some undiagnosed people tend to subconsciously avoid lots of gluten.  Cookies and cakes do not contain as much gluten as artisan breads and thick chewy pizza crust.  Anemia, diabetes and thiamine deficiency can affect IgA antibody production as well.   Do you carry genes for Celiac?  They frequently go along with EDS.
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.