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

Mcdonalds Fries Are Not Gluten Free


msserena

Recommended Posts

msserena Apprentice
Open Original Shared Link

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



Celiac.com Sponsor (A8-M):



psawyer Proficient

I assume you are referring to the statement:

Contains derivatives of wheat and dairy.

This was discussed at great length here in February. Despite this disclosure (which applies only to one source and only to the United States), independent testing has confirmed that there is no gluten in the fries. The mentioned derivatives are in a flavoring agent which is contained in the oil used in pre-processing the fries before they are frozen and shipped to the store. The disclosure is a side of effect of the new FALCPA act of 2004.

There is no wheat protein (gluten) in the derivative used to flavor this oil, which is not the frying oil used in the restaurants.

Open Original Shared Link

Disclaimer: I do not work for, own shares in, nor am in any other manner associated with McDonalds, nor have I ever been.

VydorScope Proficient
I assume you are referring to the statement:

This was discussed at great length here in February. Despite this disclosure (which applies only to one source and only to the United States), independent testing has confirmed that there is no gluten in the fries. The mentioned derivatives are in a flavoring agent which is contained in the oil used in pre-processing the fries before they are frozen and shipped to the store. The disclosure is a side of effect of the new FALCPA act of 2004.

There is no wheat protein (gluten) in the derivative used to flavor this oil, which is not the frying oil used in the restaurants.

Open Original Shared Link

Disclaimer: I do not work for, own shares in, nor am in any other manner associated with McDonalds, nor have I ever been.

Or read thier offical statement on wheat:

Open Original Shared Link

I highly recomend avioding thier fries becasue of high CC risk,(reguarldes of any gluten ingreditents) and I base that soley on my personal experences with the McDonalds near me.

VydorScope Proficient

Acuatlly more pertintant to us here is thier offical "Gluten Statement"

Open Original Shared Link

psawyer Proficient

Obviously, this is not a black-and-white issue, which is why it is important to consider all the facts before making your own decision. But, if the possibility of an undetectable trace of gluten remaining in the fries from the flavoring is a concern to you, then due to the significant cross-contamination risk, you probably should not be eating in any fast food restaurant at all.

gfp Enthusiast

The bottom line is would you trust McDonalds who have been proven in court to have lied on official statements multiple times.

here is one example:

Open Original Shared Link

However the wording is what points inthe wrong direction for me

From the other thread

McDonald's always believed that the fries were gluten-free.

answered by

If they are so innocent why the hell were they sneaky about it! If all that happened was their distributor told them what was REALLY in the fries and they REALLY didnt know before this new law what was in them, then why on earth would they just quietly release this info on their web site....just makes them look like they are trying to hide something to me.

And in regards to my prior post.....I do not think I am entitled to go eat anything anywhere....If I didnt make it I can not trust it fully!

But if a restaurant wants to tell us things are safe....they damn well better be!

If a restaurant has a gluten-free menu or a list of their ingredients you want me to believe they are doing this because they really give a damn about me or my health....NO WAY....they do it for ONE reason......To try to get/save the business of people with allergies...and thats it!

All I can say is I would much rather have a restaurant tell me that they dont know what is in their food then tell me that its safe and have it not be!

Fromt he Offical McDo release...

In conjunction with the new Food Allergen Labeling and Consumer Protection Act, our suppliers informed us

for the first time that hydrolyzed milk and hydrolyzed wheat are ingredients in the natural flavoring used in

the frying oil for the French fries and hash browns. Based on this new information, we updated nutrition

disclosures on these products on our website.

So before they were informed by their supplier they didn't ask... yet they labelled their product gluten-free....

This sounds like "lets not ask the wquestion then we are not responsible" to me or perhaps best summed up by as line from Independance Day "Two words Mr. President, plausible deniability" (or close )

Secondly they chose a specific test the "RIDASCREEN Gliadin ELISA test at a 3 parts per million level of

sensitivity."

The Ridascreen Gliadin test is a sandwich enzyme immunoassay for the quantitative analysis of gliadins from wheat and corresponding prolamines from rye and barley in food. Gluten is the characteristic term for the protein mixture of glutelins and gliadins (prolamines) found in cereals. The proportion of glutelin to gliadin in the protein mixture is approximately the same

Ridascreen Gliadin (R7001)

Detection limit: 1.5 ppm gliadine corresponding to 3 ppm (0.0003%) wheat gluten

Sample preparation: Homogenization and extraction

Incubation time: 1h 30 min

Note: The gliadin test can detect gluten from wheat, rye and barley quantitatively with a detection limit of 3 ppm.

Ridascreen Fast Gliadin (R7002)

Detection limit: 5 ppm gliadin corresponding to 10 ppm (0.001%) wheat gluten

Testing time: Approximately 1 hour.

Note: In addition to wheat gluten, the Fast Gliadin kit is 100% cross-reactive to rye and barley.

This is a production testing kit NOT a lab analysis. There is a world of difference.

If you are looking for a CYA instead of fact this is ideal and saves them circa $300 on a proper lab analysis by GC-MS which can detect ppb.

The screening tests are designed for production line screening NOT making statements about the composition.

Secondly the statement is deliberatly misleading... they quote a gliadin test but in units of gluten which in durham wheat is 0.8:1

The bottom line is McDonalds has been in court over misleading its consumers many times. Some of the cases have been wrong, some have been dropped on insufficient evidence of culpability and some have been found true. Is this really the profile of a company you want to trust?

In the end we all need to decide that for ourselves.

VydorScope Proficient
Obviously, this is not a black-and-white issue, which is why it is important to consider all the facts before making your own decision. But, if the possibility of an undetectable trace of gluten remaining in the fries from the flavoring is a concern to you, then due to the significant cross-contamination risk, you probably should not be eating in any fast food restaurant at all.

Your right, and I do not take my son to those places. When he has had McDondals fries his reaction was very bad, and very clear. CC risks are everywhere, and we accept that, but when a place like McDondals constitenly has an issue, we steer clear. I said that BEFORE this new ingredient informatoin came out, and stand by it. REGUARDLESS of any gluten in the ingredients McDondals is, in my personal experence, unable to produce gluten free fries. Same with Burger King, and etc.

There are posts on this board from employees and family of employees of McDonalds that share stores of them frieing pies, and etc in the french fryers, droping in nuggest in a rush and so on.

I guess in my eyes theres difference between the risk of CC (such as with any mainstream product) and the appearent garrenntee of CC that McDondals offers. In my personal experence I have never seen a McDondals where CC was not evident.


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



Celiac.com Sponsor (A8-M):



penguin Community Regular

Isn't this horse dead enough without beating it?

If it makes you sick, don't eat it. McDonald's is not required to disclose allergens, since they are a restaurant, not a manufacturer. They don't fall under the umbrella of the labelling law, but they volunteered to disclose that information. The FDA also does not have regulations regarding what is "gluten-free" in the US so most companies use the European codex standard of 30 ppm or less. McDonald's sent their fries to the U. of Nebraska to be tested, like many other companies do. In a lab setting, the fries are gluten-free. Like Vincent said, McDonald's or any ff place is a hotbed of cc.

Keep in mind also that gluten free menus are provided as a courtesy and as a guideline. They are not hard and fast menus, but guides of what is probably gluten-free consistently. Eating out is always a risk, especially when the employees are making minimum wage and there is poor training and high turnover. Nobody requires anybody to provide gluten-free menus.

KaitiUSA Enthusiast

I used to eat them but now I avoid them because of the recent talk about it.

gfp Enthusiast
Isn't this horse dead enough without beating it?

If it makes you sick, don't eat it. McDonald's is not required to disclose allergens, since they are a restaurant, not a manufacturer. They don't fall under the umbrella of the labelling law, but they volunteered to disclose that information. The FDA also does not have regulations regarding what is "gluten-free" in the US so most companies use the European codex standard of 30 ppm or less.

I think that is the point.

If McDonalds volunteers the information they should make sure its accurate. They have the option of not providing it if they are unsure so when they choose to make public statements and provide fact sheets they should make sure they are accurate as if they are unsure they have the option of saying so or saying nothing.

The way I see it, if they were required by legislation to provide the information and made a mistake that is one thing but to volunteer false information is a different matter be that knowoingly or by m,aking sure they ave no paperwork that proves they knew the composition of the oil. Equally if this were an isolated incident I would be more sympathetic but McDonalds has a long history of releasing inaccurate statements and the main problem is to prove mea culpa.

McDonald's sent their fries to the U. of Nebraska to be tested, like many other companies do. In a lab setting, the fries are gluten-free.
This is not a indication of diligence it is a act of CYA. They presumably chose to test using the ELISA test because it is less accurate and only semi-quantitative, I can't see a few thousand $ of GC-MS time actually being the reason they opted for the screening test rather than a real quantitive test.

If I can make a corallory

Open Original Shared Link

Open Original Shared Link

Ford clearly knew that people would be killed due to the defect but their action was to see what they might loose in litigation vs a recall. Its a simple mathematical decision on which the cost of human life is determined only by what they might be sued for..

However, why would the consumers be surprised by this.... Ford had already clearly demonstrated its position over the Pinto

Open Original Shared Link

The point I am trying to make is some companies operate like this. McDonalds has been proven in court on many many occaisions to have deliberatly released false information. The link I made above (prior post) links to just one case, but its a recent US case and yet it appears most people are unaware of it.

penguin Community Regular

Conspiracy theories aside, nobody is forcing you to buy anything from them.

I commend them for taking the fries of the gluten-free list. And for having a gluten-free list at all.

gfp Enthusiast
Conspiracy theories aside, nobody is forcing you to buy anything from them.

I commend them for taking the fries of the gluten-free list. And for having a gluten-free list at all.

Its not a conspiracy theory that McDonalds lie about their ingredients, it is a matter of court record.

All I am expressing is "are they the sort of company you want to trust" and as I said earlier that is an individual matter everyone can decide for themselves.

I find it surprising that poeople have not read of the previous cases (like the one I posted) and I am merely seeking to bring this to peoples attention so they can decide for themselves. Personally I prefer top trust people and organisations until they do something to prove me wrong and in the case of ford and Mcdonalds they have already done this so I would be a fool to trust them...."Fool me once shame on you..." (add the ending of your choice here :D)

The reason I hesititate to commend them is because they had the fries on a gluten-free list but never asked the manufacturers of the oil. So whereby its good they have taken them off now I question their motivation ... for instance if they got a different supplier who would give them a certificate of gluten-free compliance (for instance to codex standards) and they knew it contained gluten anyway I don't think they have the interest of their customers at heart. My reasoning on this is the multiple court cases that have proven them to be deliberatly covering up ingredients.

They may have changed? Who knows but for me they have shown their colors and they will need to do something more than take gluten-free fires off the list to convince me they are interested in providing their customers with nutritional infomation.

I realize supersize-me is a commerical film and they guy made money from making it but in nearly all the McDo's he went to the nutritional info was unavailable and McDonalds have yet to sue him or issue a correction so considering they are court happy I am happy to accept they say one thing but practice another.

Archived

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

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

    • Total Members
      133,258
    • Most Online (within 30 mins)
      7,748

    Tdodge
    Newest Member
    Tdodge
    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)

  • Upcoming Events

  • Posts

    • suek54
      Wow KK, thank you so much for all your attached info. I had a very quick scan but will read more in depth later.  The one concerning corticosteroid use is very interesting. That would relate to secondary adrenal insufficiency I think , ie AI caused by steroids such as taken long term for eg asthma. I have primary autoimmune AI, my adrenals are atrophied, no chance if recovery there. But I am in touch with some secondaries, so something to bear in mind. .  Niacin B3 Very interesting too. Must have a good read about that.  Im sure lots of questions will arise as I progress with dermatitis herpetiformis. In the mean time, thanks for your help.
    • knitty kitty
      Welcome to the forum, @suek54, I have Dermatitis Herpetiformis, too.  I found taking Niacin B3 very helpful in clearing my skin from blisters as well as improving the itchies-without-rash (peripheral neuropathy).  Niacin has been used since the 1950's to improve dermatitis herpetiformis.   I try to balance my iodine intake (which will cause flairs) with Selenium which improves thyroid function.   Interesting Reading: Dermatitis herpetiformis effectively treated with heparin, tetracycline and nicotinamide https://pubmed.ncbi.nlm.nih.gov/10844495/   Experience with selenium used to recover adrenocortical function in patients taking glucocorticosteroids long https://pubmed.ncbi.nlm.nih.gov/24437222/   Two Cases of Dermatitis Herpetiformis Successfully Treated with Tetracycline and Niacinamide https://pubmed.ncbi.nlm.nih.gov/30390734/   Steroid-Resistant Rash With Neuropsychiatric Deterioration and Weight Loss: A Modern-Day Case of Pellagra https://pmc.ncbi.nlm.nih.gov/articles/PMC12532421/#:~:text=Figure 2.,(right panel) upper limbs.&text=The distribution of the rash,patient's substantial response to treatment.   Nicotinic acid therapy of dermatitis herpetiformis (1950) https://pubmed.ncbi.nlm.nih.gov/15412276/
    • suek54
      Thank you all for your advice and the dermatitis herpetiformis article. The latter made me realise I had stopped taking my antihistamine, which I will restart today. The Dapsone has cleared the rash entirely but I still get quite a bit itching, absolutely nothing to see though. I know its notoriously hard to clear and its still relatively early days for me.  The iodine issue is very interesting. I do eat quite a bit of salt because I have Addison's disease and sodium retention is an issue. I also have autoimmune hypothyroidism, not sure how a low iodine diet would play into that? Because of my Addison's I am totally steroid dependent, I take steroids 4 x daily and cannot mount any defence against inflammation. I need to increase my meds for that. Now that I know what is wrong I can do just that if Im having a bad day. Life is very sweet, just so damn complicated sometimes! Hey ho, onwards. Thank you again for your advice.  
    • 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!!! 
×
×
  • 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.