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

Barley malt vinegar extract in Kettle crisps - safe?


rarchy

Recommended Posts

rarchy Apprentice

Just wanted to see if you guys eat or avoid dried barley malt vinegar in crisps etc? I saw it was considered an allergen in the ingredients (http://www.kettlefoods.co.uk/our-hand-cooked-chips/kettle-chips/flavour/sea-salt-and-balsamic-vinegar/ingredients/) and so assumed it should be avoided, however I have since read conflicting information including on Coeliac UK's website - https://www.coeliac.org.uk/frequently-asked-questions/can-i-eat-barley-malt-vinegar/ 

In fact those crisps in question are on Coeliac UKs suitable to eat list in their food directory!

It seems very strange that the general advice is to not eat food such as Walkers crisps which don't even necessarily contain gluten but just have the warning "Made in the same factory as....", but something which actually contains gluten is apparently safe? 

Thoughts?


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



Celiac.com Sponsor (A8-M):



Ennis-TX Grand Master

We always say check the ingredients, even if it used to be gluten-free manufactures constantly change the recipe and you have to check the ingredient list on foods to be sure. I think that might be the case of why you find the product on the suitable list. Here in the US anything with barley extract or barley malt is not considered gluten-free. We have had multiple cases in the past year of companies trying to label products gluten-free that contain those. These are normally called out by consumers or groups like Gluten Free Watch dog who contact the proper people to have said products pulled from the shelves.

 

rarchy Apprentice

Hi Ennis, thanks for the reply. I don't think they have changed the ingredients, as far as I know the barley malt vinegar has always been there, and the Coeliac UK list is pretty up to date I believe. Its weird as Coeliac Uk actually say on their website that barley malt vinegar is ok! I will give it a miss if this is what others do, best not to take the risk. 

Jmg Mentor
6 minutes ago, rarchy said:

Its weird as Coeliac Uk actually say on their website that barley malt vinegar is ok! I will give it a miss if this is what others do, best not to take the risk. 

Coeliac UK occasionally strike a controversial note. I often saw arguments online about recommendations. I think they're generally guided by the prevailing science. 

My barley malt story is that I joined CUK and the guide became my Bible in the first months on the diet. One item on there was Aldi cornflakes, I like Aldi and some months later I saw them and decided to have them even though they listed barley malt on the box. I felt weird eating something with the forbidden ingredient but they were on the safe list so....

Within a few days I get a very itchy rash on my elbows. It's driving me mad and I put two and two together, the damned cornflakes!  I bin them and the rash luckily goes quickly. I check and on the new guide list the cornflakes have gone. Maybe they changed their recipe or maybe they should never have been listed in first place...

So although there's advice out there that barley malt levels in some cereals are low enough to tolerate I will never again risk it. Others may have a different view.

I would never have barley malt vinegar in liquid form. Thats definitely a problem. There are also salt and vinegar crisps out there without the barley in, I look for the cider vinegar ones although you still have to check the ingredients. With Kettle I eat the salted ones and not the salt and vinegar. 

rarchy Apprentice

Thanks thats good to know, I did think some of what Coeliac UK said seemed to contrast with actual celiacs and their experiences. I am definitely going to stay on the stricter side. 

I have their food guide in printed form and the app, but to be honest I have just been checking the ingredients of whatever I buy, like we discussed my other post if it mentions "may contain..."  etc I will avoid. I am trying to eat less processed food now anyway so that makes it easier. 

In fact I kind of wonder what purpose the guide serves seeing as allergens have to be listed in ingredients (I know this wasn't the case pre-2014), isn't it just easiest to look at the ingredients that check a book/app each time, or is it because the foods in there are safe for cross contamination? 

  • 2 years later...
Ems67 Newbie

Hi

Just saw this post and wanted to add to it. 

Yesterday I had a packet of the Kettle salt and vinegar crisps

Ended up with blood blisters in my mouth which is my reaction to anything gluten as well as bleeding gums when I clean my teeth

So lesson learnt!!!

 

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

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Katya773 posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      0

      Wholefoods 365 Organic Wheatgrass Powder

    2. - emily 1 replied to emily 1's topic in Coping with Celiac Disease
      8

      Black Pepper Reactions

    3. - Blue Roan replied to emily 1's topic in Coping with Celiac Disease
      8

      Black Pepper Reactions

    4. - Blue Roan posted a topic in Related Issues & Disorders
      0

      Irregular periods AFTER going gluten-free?

    5. - John Scott commented on dixonpete's blog entry in Pete Dixon
      9

      A video with researcher William Parker about Helminthic Therapy


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      127,010
    • Most Online (within 30 mins)
      7,748

    Susan A.Knapp
    Newest Member
    Susan A.Knapp
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121k
    • Total Posts
      69.8k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Katya773
      Hi Everyone,   I recently purchased this wheatgrass not realizing that it wasn’t gluten free. I had two servings before I got really sick. Abdominal cramps , diarrhea and horrible nausea. My daughter read the label and told me it wasn’t labeled gluten free. I thought this was safe because supposedly it’s healthy. I called WholeFoods and they told me that they can find out more about the product and email me when it was picked and harvested. I was diagnosed back in 2019 and I really should know better! Anyone else had a reaction to wheatgrass powder? 
    • emily 1
      Yes, unfortunately I was diagnosed about 15 years ago. Some of us I guess the gut never heals and from what I've learned you can actually have a setback which is probably the stage I am at where I actually have become more sensitive to more items.
    • Blue Roan
      Hi Emily! I was just diagnosed a year ago and could not touch nuts, corn (or anything with corn-based ingredients), lactose, or black pepper in the first 8 or so months. Otherwise I had a lot of abdominal discomfort, dizziness/vertigo (especially with corn and pepper) and inflammation throughout the body. I was pretty much eating plain cooked veggies and chicken for the first few months because they were safe and reliable.  Over time, I have slowly started to tolerate some of the no-no foods, but my system is still sensitive to the pepper and has a limit to corn/lactose before symptoms occur. When you’re first diagnosed, you will likely be sensitive to a lot of other foods because your gut is healing from the damage and your body needs to reset. I find that keeping a food diary  and only slowly introducing other foods back into your diet over time is helpful. It is frustrating to feel so limited, but give it some time and patience. It can take the gut years to fully heal in many cases. 
    • Blue Roan
      Hi there, I am 30 and was diagnosed with celiac almost a year ago after a series of severe “unexplained” abdominal episodes. Everything is improving and I am feeling so much better overall except my cycle is worse. Has anyone else had a similar experience?  I got my period as a pre-teen and my cycles have been regular for as long as I can remember: every 21 days, lasting 5 days. My periods were heavy and I always had severe cramping at the start that subsided after the first two days.  I went gluten-free immediately when I was diagnosed in February. At first, my cycles were the same but around July, I started noticing very crazy symptoms around that time of the month: chills all over the body, severe headaches, some hot flashes, dry mouth and then cramps starting a few days earlier than usual. My cycles also started happening later and later. This time around, I’m on Day 35 and no period so far, but still cramping/abdominal pain/nausea on and off for the past week. It has been feeling like it’s about to happen any minute but nothing. I even get the pelvic contractions/pains but nothing after. I cannot sleep from all the hormonal fluctuations and chills. I can confirm I am not pregnant.  I’ve seen the endocrinologist, OBGYN, primary, and multiple gastro doctors throughout the year. No IBD ( but possible IBS), thyroid panel normal, thyroid ultrasound normal, negative for Hashimoto’s. I had a full vitamin panel and all levels normal (no anemia or vitamin B deficiency). After some testing, the gyn thinks PCOS is highly unlikely and that my body is “still adjusting” to going gluten-free. I’ve been strict gluten-free for nearly a year though.   All of my regular labs are normal and my antibodies are on a downward trend. I am really confused because more of my research points to the gluten-free diet resulting in better cycles rather than the opposite. While my cycles are not as heavy, they’re more unpredictable and uncomfortable with all these new symptoms. 
    • Mari
      Hi Emily, What you described is very similar to what I experienced in coping with Celiacs. I think my first symptoms started when I was about 3 and I wasn't diagnosed until I was almost 70. I got along OK util I was about 30  when I began to have more problems that the Drs thought was an autoimmune problem that they couldn't identify. Then I worked in medical labs in Bolivia for 8 months and returned to the US with more problems such as sensitivities to chemicals and increasing food intolerances. I had always had canker sores in my mouth and nose but have not had any now  since I went strictly gluten free. Before I was gluten-free I became very sensitive to hot peppers and then I could not eat anything spicy such as cinnamon, turmeric or black peppers. I have not eaten any nightshades for years. No corn or soy.  My diet now is lamb stew with rice, squash, green beans, chard, kale, collards with salt. Then eggs , chard, spinach, black beans, summer squash, asparagus, rice and salt. I eat peanuts for snacks. I have been eating nuts but may have to stop. Coconut is OK but too much sugar is not.  I am very cautious about adding back foods to my diet but hope to add back small amounts of turmeric. Take care.
×
×
  • Create New...