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

Franz Gluten Free Bread Products


Chiqeeey

Recommended Posts

Chiqeeey Newbie

Beginning in October 2021, I began experiencing problems with Franz gluten-free Seven Grain Bread.  I was paying $7.50 a loaf for air.

Then the same thing started happening with the hamburger buns.  I have photos of the products but I do not know how to add them to 

this topic.  Don't get me wrong,  I like the taste of the Franz gluten-free breads, especially the hamburger buns.

I emailed Franz and I was sent complimentary coupons for free bread.  When I emailed a second time about the air in the hamburger buns, I received a 

box of white bread, seven grain bread and the hamburger buns.  Plus they threw in a new product (new to me) frozen cookie dough.  Has anyone tried those yet?

They are plant based.  But I digress.

Last night, I opened the hamburger buns and took one bun.  There are four in a package.  I split it in half and globbed on a bunch of butter.  When I put the last 

piece in my mouth, I bit down on something hard.  I thought it was a piece of tooth.  Low and behold, it was a straight pin.  I don't know how it didn't stick into 

my tongue or cheek.  Thank God for that.  I immediately took a picture and sent it in an email to Franz last night.  I have yet to hear back from them. 

I have a friend who used to buy the Franz gluten-free bread.  She got tired of paying for crust only.  She just stopped buying it.  Has anyone else had this problem?


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



Celiac.com Sponsor (A8-M):



Scott Adams Grand Master

I've been eating their bread for years without any issues, and I get the two loaves at Costco for a much better price than any other gluten-free bread I can find. As you know, its also a whole grain bread, which is great.

The only issues I've noticed is that occasionally there are large air bubbles in some of the loaves, which can be annoying, but I found this to also happen with all other GF breads I've tried.

The pin issue is a real problem, and it's good that you reported it. Wow...I wonder how that happened?

Chiqeeey Newbie
18 hours ago, Scott Adams said:

I've been eating their bread for years without any issues, and I get the two loaves at Costco for a much better price than any other gluten-free bread I can find. As you know, its also a whole grain bread, which is great.

The only issues I've noticed is that occasionally there are large air bubbles in some of the loaves, which can be annoying, but I found this to also happen with all other gluten-free breads I've tried.

The pin issue is a real problem, and it's good that you reported it. Wow...I wonder how that happened?

About 10 years ago, my husband bought the Bready machine.  It came with prepackaged bread mix.  The label was scanned by the machine and then the bag was placed on the machine.  All that was needed was to add eggs and water.  The machine mixed the ingredients, kneaded it and poured in a pan.  Then it baked the mix to a delicious smelling loaf of bread.  The rye bread was to die for.  There were never any holes in the slices.  The machine and the mixes were very expensive but I thought it was worth it.  Then the company disappeared.  We could not order any more mixes.  I believe the company was based in Kansas.  We gave the machine away because it was useless without the bag of mixes.   

Scott Adams Grand Master

I remember Bready! You can use recipes in any bread machine, but too late! I suspect when Panasonic and other big companies got into the space it likely hurt their sales:

 

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
      130,704
    • Most Online (within 30 mins)
      7,748

    Beth Clower
    Newest Member
    Beth Clower
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Grahamsnaturalworld
      Where can I find a gastro in adelaide who can diagnose refractory celiac disease have seen 3 so far and don't understand the most obvious question, why my celiac symptoms did not resolve on a gluten free diet the symptoms just got worse as it is attacking my nervous system. 
    • ShariW
      I recently traveled to Spain and Portugal. I was with a tour group, they knew I needed to be gluten-free and made sure the kitchens preparing the group meals were aware. But just in case, I took Gliadin-X with me and took it for every evening meal - and most other meals. The one time I got glutened was from lunch early in the trip - had to be from cross-contamination. I had not taken Gliadin-X before that meal, which made for a pretty miserable day. Learned my lesson... 😞 
    • Hummer01
      Hi trents, thanks for the response.  The 2nd opinion doctor said that if my CRP is still elevated at that time, he would advise me to look at Crohns/UC or another autoimmune issue. The colonoscopy I had this year seemed to rule those 2 out for now so he still believed celiac may explain it. No previous doctors have suggested any explanation for it even after calling to tell me it was a concerning result.  I guess it feels tough knowing I have positive blood testing, permissive genetics, and visible duodenum changes... and somehow it's NCGS instead of celiac. I'm still surprised the biopsies came back negative when the doctor was so sure they would be positive.
    • trents
      "He also said that my CRP should return to a normal level at this time if the culprit was inflammation in the small intestine due to celiac." But with if the elevated CRP levels are caused by some other inflammatory process going on in your body? "She also said that my positive EMA isn't valuable because it has "a high false positive rate." Totally wrong! This is a highly accurate test for celiac disease, that requires specialized expertise to perform and interpret, and it is more expensive than other blood tests. It is generally used as a last test to confirm celiac disease after a positive tTG-IgA test. The sensitivity of a test refers to its ability to correctly identify individuals with the condition. For the EMA-IgA blood test, the sensitivity is generally very high, ranging from 90% to 98%. This means that the test can accurately detect celiac disease in a significant percentage of people who have the condition. The specificity of a test refers to its ability to correctly identify individuals without the condition. For the EMA-IgA blood test, the specificity is also high, typically around 95% to 100%. This indicates that the test can effectively rule out celiac disease in individuals who do not have the condition. Taken from the following article: Looking at the whole picture, I am wondering if you are transitioning from NCGS to celiac disease. Some experts in the gluten disorder field believe NCGS can be a precursor to celiac disease.
    • Hummer01
      Hi all, just wanted to post an update.  I have been gluten free for about 1.5 months now and seeing improvement already in the bathroom.  Recently I had a visit with another GI doctor for a 2nd opinion. He said that while my blood tests and scope are not a "slam dunk" for celiac, he believes it's more likely than not that I have it. His advice was to stay with a celiac-level gluten free diet (no CC) for 6-12 months then retest to make sure TTG-IGA is still negative. He also said that my CRP should return to a normal level at this time if the culprit was inflammation in the small intestine due to celiac.  Today I had a follow up with the original GI that performed the scope. She is confident it is NCGS and says I can still have gluten sometimes. When I asked about the visible duodenum damage, she said it is just "irritation" from gluten because the biopsies were negative. She also said that my positive EMA isn't valuable because it has "a high false positive rate."  I guess I'm having trouble reconciling the totally different advice from these 2 GI's. I want to believe the new doctor more at this point because what he said just makes more sense to me, and he gave an actionable timeline for possible next steps. Feeling lost and disappointed at this point and wanted to write it down here in case anyone has input. Thank you.   
×
×
  • Create New...