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

How Big Of A Problem Is Cc With Canned Products?


Asharia

Recommended Posts

Asharia Rookie

I am trying to figure out sources of cross contamination in products I use, and I am not sure how diligent I need to be with canned foods that don't have any gluten ingredients - for example, fire-roasted tomatoes or refried beans, or even just plain black beans!

It seems like CC would be more likely with a brand that makes tons of stuff(like Trader Joe's or 365) than a more specialized brand?

If you are super sensitive, what brands do you prefer?


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



Celiac.com Sponsor (A8-M):



Marilyn R Community Regular

Dear Asharia,

Hello & welcome to the forum! I was sensitive at first (18 months), but it seems like my autoimmune system is starting to simmer down. During the first year I had a few more obstacles.

Soy, dairy and corn kicked me right in the gut. I'm good with dairy now, haven't tried reintroducing corn or soy. I also had problems with quinoa and oats. My reactions were so severe that I'll probably never try them again, but that doesn't mean that you will a problem with those grains. I find plenty of good things to eat without those grains! There are so many good things we can eat without problems.

T.H. Community Regular

There can definitely be gluten cc issues with canned goods, but at least in my experience, it depends on the product and the brand quite a bit.

Some brands make a lot of their products in the same facility, so that can up the risk. But some companies that make a lot of products have separate facilities for separate products. Often seems to depend on the product's popularity. Canned tomatoes, for example, sell enough that they are often made in facilities completely devoted to processing tomatoes (same can be said of olive oil, often).

Soups I would be more wary of, as I imagine they are more likely to be made in facilities and on lines that are shared with other soups, which could be gluten cc'd

Beans may have the same issue. I'd check out the company. Some of the big companies like Heinz, Hunts, etc... will let you know what they consider gluten free. I'll admit, I've had a hard time with beans, because the DRIED beans seem to so often be processed in facilities that process wheat. I don't know if the canning companies get their beans from similar places, but it could be an issue, if you are really sensitive.

If you are super sensitive, what brands do you prefer?

I have given up on canned goods, at this point. I've just gotten sick too many times. I get buy dry beans, wash them with soap and water in a wire mesh collander, and make them myself. I know of one sensitive gentleman who was having good luck with many of the dried beans at Albertsons, so that wasn't too expensive. I'm getting the veggies fresh now and making stuff myself...very, very slowly, LOL.

Lisa Mentor

Welcome to the Board!

When you first begin the Gluten Free Diet after some time with major digestive issues, it may be an etended time to restore order to your digestive system. Every food, whether gluten free or not, will be bothersome.

Eat simply, eat fresh and don't worry about cross contamination.

Learn to read labels and listen to your body as you reach toward the road to recovery....life is out there. :D

Take one step at a time!

Lisa Mentor

There can definitely be gluten cc issues with canned goods, but at least in my experience, it depends on the product and the brand quite a bit.

Gluten Free canned goods are normally the least of my concerns. I would seek other possible cross contamination sources.

weluvgators Explorer

Hi, Asharia! Welcome to the board. :D

I see that you are trying to figure out your elevated antibody issues that have resurfaced and that you are seeking input from those that consider themselves super sensitive. With my disclaimer that our family is super sensitive, we have found that we needed to eliminate most of our canned goods. I have had "gluten free" labelled canned beans turn up positive in a gluten detection home test that I use. For beans, we now buy our dry beans in bulk from a GFCO certified source, test them per our household quality assurance program (our supply has tested negative for gluten to date), and then wash them thoroughly.

For tomatoes, we greatly reduced our reliance on canned tomato products produced by others by producing a large amount of tomato sauce from a carefully sourced supplier that was willing to discuss and disclose growing practices of their food. Someone recently reported on Muir Glen's response to their inquiry, and it was hardly confidence building: .

If you read the 20 PPM thread, I feel that there are plenty of people advocating that you should reduce all of this "processed food" consumption and do most of the processing yourself. I haven't figured out a safer way to feed my super sensitive family than to do just that - process almost all of our own food. It was truly eye opening to get back to the basics of ensuring proper whole foods sourcing!

I agree with the eat simply, eat fresh, although eating fresh would have been far more difficult for me during other periods in my life . . . not sure what your current circumstances are. But I disagree about not worrying about cross contamination. I haven't checked, and you specifically asked here about products, but have you done a thorough review of all of the other potential sources of cross contamination? We didn't get to the canned foods issue until we had been gluten free for a few years, and we were trying to address some underlying, complicating issues. Do you have a shared kitchen / living space? Have you replaced and maintained all of the necessary kitchen items? Have you made any changes in your personal care, toiletries, or makup items? And the Amy's and Trader Joes stuff that you mention in another thread - we had to drop both of those long before we noticed any issues with a minority of the canned goods that still end up on our shelves occasionally!

Good luck figuring this out, and I hope that your antibody levels return to normal soon!

Asharia Rookie

Thanks for all of your thoughts - although I am disappointed that there is not something not completely fresh that I don't have to worry about :) It does seem like cutting out Trader Joes and Amy's products are a good start, but part of me just wants to go all the way to make sure I start feeling better sooner. Thinking about going all non-processed is as stressful as going gluten-free was in the beginning for me, 4 years ago. Unfortunately, I don't like to cook, but perhaps that has to change.

I have tried to be very careful with other things - I know my toiletries and shampoos are ok, and I live alone and no gluten has touched my toaster oven or strainer, although I used to live with gluteny roommates - but supposedly you can wash gluten off of most things. The Tums and Zantac I eat like candy are too! Even my dog is (mostly) gluten-free :)

What about frozen veggies!?

Hi, Asharia! Welcome to the board. :D

I see that you are trying to figure out your elevated antibody issues that have resurfaced and that you are seeking input from those that consider themselves super sensitive. With my disclaimer that our family is super sensitive, we have found that we needed to eliminate most of our canned goods. I have had "gluten free" labelled canned beans turn up positive in a gluten detection home test that I use. For beans, we now buy our dry beans in bulk from a GFCO certified source, test them per our household quality assurance program (our supply has tested negative for gluten to date), and then wash them thoroughly.

For tomatoes, we greatly reduced our reliance on canned tomato products produced by others by producing a large amount of tomato sauce from a carefully sourced supplier that was willing to discuss and disclose growing practices of their food. Someone recently reported on Muir Glen's response to their inquiry, and it was hardly confidence building: .

If you read the 20 PPM thread, I feel that there are plenty of people advocating that you should reduce all of this "processed food" consumption and do most of the processing yourself. I haven't figured out a safer way to feed my super sensitive family than to do just that - process almost all of our own food. It was truly eye opening to get back to the basics of ensuring proper whole foods sourcing!

I agree with the eat simply, eat fresh, although eating fresh would have been far more difficult for me during other periods in my life . . . not sure what your current circumstances are. But I disagree about not worrying about cross contamination. I haven't checked, and you specifically asked here about products, but have you done a thorough review of all of the other potential sources of cross contamination? We didn't get to the canned foods issue until we had been gluten free for a few years, and we were trying to address some underlying, complicating issues. Do you have a shared kitchen / living space? Have you replaced and maintained all of the necessary kitchen items? Have you made any changes in your personal care, toiletries, or makup items? And the Amy's and Trader Joes stuff that you mention in another thread - we had to drop both of those long before we noticed any issues with a minority of the canned goods that still end up on our shelves occasionally!

Good luck figuring this out, and I hope that your antibody levels return to normal soon!


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



Celiac.com Sponsor (A8-M):



Lisa Mentor

Just a quick note here:

Tums-all are gluten-free except as noted below

Tums Smoothies-Most varieties of TUMS Smoothies are gluten free. Only

TUMS Smoothies Cocoa and Cream contain gluten (5/5/2011)

kareng Grand Master

Not to scare Newbies:

For most Celiacs, canned & frozen veggies are fine. Just read the ingredients. There is very little reason for most of us to worry.

Your first post on here didn't specify you have been gluten-free for years and having problems. You must have said that somewhere else. We do have a section for super sensitives that might be worth you taking a look at. :)

Skylark Collaborator

I am trying to figure out sources of cross contamination in products I use, and I am not sure how diligent I need to be with canned foods that don't have any gluten ingredients - for example, fire-roasted tomatoes or refried beans, or even just plain black beans!

It seems like CC would be more likely with a brand that makes tons of stuff(like Trader Joe's or 365) than a more specialized brand?

If you are super sensitive, what brands do you prefer?

I just answered your other thread. If I had your issues with celiac antibodies staying high for no reason, I would stop eating processed foods. Period. Get the antibodies to go down and then start to figure out what you can tolerate. You can tell there is no gluten in a scrubbed, whole tomato. You can't tell if there is a trace of gluten in a can of them without testing. Most of us tolerate canned foods just fine, but I think you need to get back to basics.

  • 5 years later...
keezyfresh Apprentice
On 25/09/2011 at 8:30 PM, T.H. said:

I'll admit, I've had a hard time with beans, because the DRIED beans seem to so often be processed in facilities that process wheat. I don't know if the canning companies get their beans from similar places, but it could be an issue, if you are really sensitive.

The reason there is often a "may contain wheat" statement on dried/canned legumes, as far as I know, is because it is extremely common for legumes to be grown in a crop rotation cycle with gluten grains (on the same field but at different times) because growing them in rotation can help enhance the production of each crop. I would assume that it's also common for the two crops to be processed in shared facilities, but it's important to note that even if beans/other legumes are processed in a facility that doesn't deal with gluten items, there can still be a significant risk of cross-contamination if the legumes are grown on shared fields, as is apparently quite commonly practiced. 

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - trents replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      3

      how much gluten do I need to eat before blood tests?

    2. - catnapt replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      3

      how much gluten do I need to eat before blood tests?

    3. - trents replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      3

      how much gluten do I need to eat before blood tests?

    4. - catnapt posted a topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      3

      how much gluten do I need to eat before blood tests?

    5. - trents replied to McKinleyWY's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      4

      Accuracy of testing concerns

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      133,256
    • Most Online (within 30 mins)
      7,748

    Christie Fassel
    Newest Member
    Christie Fassel
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Who's Online (See full list)

    • There are no registered users currently online
  • Upcoming Events

  • Posts

    • trents
      So, essentially all of the nutrition in the food we eat is absorbed through the villous lining of the small bowel. This is the section of the intestinal track that is damaged by celiac disease. This villous lining is composed of billions of finger-like projections that create a huge amount of surface area for absorbing nutrients. For the celiac person, when gluten is consumed, it triggers an autoimmune reaction in this area which, of course, generates inflammation. The antibodies connected with this inflammation is what the celiac blood tests are designed to detect but this inflammation, over time, wears down the finger-like projections of the villous lining. Of course, when this proceeds for an extended period of time, greatly reduces the absorption efficiency of the villous lining and often results in many and various nutrient deficiency-related health issues. Classic examples would be osteoporosis and iron deficiency. But there are many more. Low D3 levels is a well-known celiac-caused nutritional deficiency. So is low B12. All the B vitamins in fact. Magnesium, zinc, etc.  Celiac disease can also cause liver inflammation. You mention elevated ALP levels. Elevated liver enzymes over a period of 13 years was what led to my celiac diagnosis. Within three months of going gluten free my liver enzymes normalized. I had elevated AST and ALT. The development of sensitivities to other food proteins is very common in the celiac population. Most common cross reactive foods are dairy and oats but eggs, soy and corn are also relatively common offenders. Lactose intolerance is also common in the celiac population because of damage to the SB lining.  Eggs when they are scrambled or fried give me a gut ache. But when I poach them, they do not. The steam and heat of poaching causes a hydrolysis process that alters the protein in the egg. They don't bother me in baked goods either so I assume the same process is at work. I bought a plastic poacher on Amazon to make poaching very easy. All this to say that many of the issues you describe could be caused by celiac disease. 
    • catnapt
      thank you so much for your detailed and extremely helpful reply!! I can say with absolute certainty that the less gluten containing products I've eaten over the past several years, the better I've felt.   I wasn't avoiding gluten, I was avoiding refined grains (and most processed foods) as well as anything that made me feel bad when I ate it. It's the same reason I gave up dairy and eggs- they make me feel ill.  I do have a bit of a sugar addiction lol so a lot of times I wasn't sure if it was the refined grains that I was eating - or the sugar. So from time to time I might have a cookie or something but I've learned how to make wonderful cookies and golden brownies with BEANS!! and no refined sugar - I use date paste instead. Pizza made me so ill- but I thought it was probably the cheese. I gave up pizza and haven't missed it. the one time I tried a slice I felt so bad I knew I'd never touch it again. I stopped eating wheat pasta at least 3 yrs ago- just didn't feel well after eating it. I tried chick pea pasta and a few others and discovered I like the brown rice pasta. I still don't eat a lot of pasta but it's nice for a change when I want something easy. TBH over the years I've wondered sometimes if I might be gluten intolerant but really believed it was not possible for me to have celiac disease. NOW I need to know for sure- because I'm in the middle of a long process of trying to find out why I have a high parathyroid level (NOT the thyroid- but rather the 4 glands that control the calcium balance in your body) I have had a hard time getting my vit D level up, my serum calcium has run on the low side of normal for many years... and now I am losing calcium from my bones and excreting it in my urine (some sort of renal calcium leak) Also have a high ALP since 2014. And now rapidly worsening bone density.  I still do not have a firm diagnosis. Could be secondary HPT (but secondary to what? we need to know) It could be early primary HPT. I am spilling calcium in my urine but is that caused by the high parathyroid hormone or is it the reason my PTH is high>? there are multiple feedback loops for this condition.    so I will keep eating the bread and some wheat germ that does not seem to bother me too much (it hasn't got enough gluten to use just wheat germ)    but I'm curious- if you don't have a strong reaction to a product- like me and wheat germ- does that mean it's ok to eat or is it still causing harm even if you don't have any obvious symptoms? I guess what you are saying about silent celiac makes it likely that you can have no symptoms and still have the harm... but geez! you'd think they'd come up with a way to test for this that didn't require you to consume something that makes you sick! I worry about the complications I've been reading about- different kinds of cancers etc. also wondering- are there degrees of celiac disease?  is there any correlation between symptoms and the amnt of damage to your intestines? I also need a firm diagnosis because I have an identical twin sister ... so if I have celiac, she has it too- or at least the genetic make up for having it. I did have a VERY major stress to my body in 2014-2016 time frame .. lost 50lbs in a short period of time and had severe symptoms from acute protracted withdrawal off an SSRI drug (that I'd been given an unethically high dose of, by a dr who has since lost his license)  Going off the drug was a good thing and in many ways my health improved dramatically- just losing 50lbs was helpful but I also went  off almost a dozen different medications, totally changed my diet and have been doing pretty well except for the past 3-4 yrs when the symptoms related to the parathyroid issue cropped up. It is likely that I had low vit D for some time and that caused me a lot of symptoms. The endo now tells me that low vit D can be caused by celiac disease so I need to know for sure! thank you for all that great and useful information!!! 
    • trents
      Welcome, @catnapt! The most recent guidelines are the daily consumption of a minimum of 10g of gluten (about the amount found in 4-6 slices of wheat bread) for a minimum of two weeks. But if possible stretching that out even more would enhance the chances of getting valid test results. These guidelines are for those who have been eating gluten free for a significant amount of time. It's called the "gluten challenge".  Yes, you can develop celiac disease at any stage of life. There is a genetic component but also a stress trigger that is needed to activate the celiac genes. About 30-40% of the general population possesses the genetic potential to develop celiac disease but only about 1% of the general population actually develop celiac disease. For most with the potential, the triggering stress event doesn't happen. It can be many things but often it is a viral infection. Having said that, it is also the case that many, many people who eventually are diagnosed with celiac disease probably experienced the actual onset years before. Many celiacs are of the "silent" type, meaning that symptoms are largely missing or very minor and get overlooked until damage to the small bowel lining becomes advanced or they develop iron deficiency anemia or some other medical problem associated with celiac disease. Many, many are never diagnosed or are diagnosed later in life because they did not experience classic symptoms. And many physicians are only looking for classic symptoms. We now know that there are over 200 symptoms/medical problems associated with celiac disease but many docs are only looking for things like boating, gas, diarrhea. I certainly understand your concerns about not wanting to damage your body by taking on a gluten challenge. Your other option is to totally commit to gluten free eating and see if your symptoms improve. It can take two years or more for complete healing of the small bowel lining once going gluten free but usually people experience significant improvement well before then. If their is significant improvement in your symptoms when going seriously gluten free, then you likely have your answer. You would either have celiac disease or NCGS (Non Celiac Gluten Sensitivity).
    • catnapt
      after several years of issues with a para-gland issue, my endo has decided it's a good idea for me to be tested for celiac disease. I am 70 yrs old and stunned to learn that you can get celiac this late in life. I have just gradually stopped eating most foods that contain gluten over the past several years- they just make me feel ill- although I attributed it to other things like bread spiking blood sugar- or to the things I ate *with* the bread or crackers etc   I went to a party in Nov and ate a LOT of a vegan roast made with vital wheat gluten- as well as stuffing, rolls and pie crust... and OMG I was so sick! the pain, the bloating, the gas, the nausea... I didn't think it would ever end (but it did) and I was ready to go the ER but it finally subsided.   I mentioned this to my endo and now she wants me to be tested for celiac after 2 weeks of being on gluten foods. She has kind of flip flopped on how much gluten I should eat, telling me that if the symptoms are severe I can stop. I am eating 2-3 thin slices of bread per day (or english muffins) and wow- it does make me feel awful. But not as bad as when I ate that massive amnt of vital wheat gluten. so I will continue on if I have to... but what bothers me is - if it IS celiac, it seems stupid for lack of a better word, to intentionally cause more damage to my body... but I am also worried, on the other hand, that this is not a long enough challenge to make the blood work results valid.   can you give me any insight into this please?   thank you
    • trents
      The biopsy looks for damage to the mucosal lining of the small bowel from the inflammation caused by celiac disease when gluten is ingested. Once you remove gluten from the diet, inflammation subsides and the mucosal lining begins to heal. 
×
×
  • 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.