Le Petit Outre Whole Wheat Bread Recall: Undeclared Soy
Le Petit Outre recalls 32 oz Whole Wheat Bread due to undeclared soy lecithin. Check your UPC and pull dates if affected.
Stop using this now
Whole Wheat Bread is recalled due to undeclared soy lecithin. The soy allergen is present in DDA pan spray (release agent) and the firm used it to spray the loaf pans.
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What happened, in plain English
Great Northern Bakehouse Inc. dba Le Petit Outre is recalling 32 oz loaves of Whole Wheat Bread because they contain undeclared soy lecithin. The soy allergen was present in the DDA pan spray used on the loaf pans. This poses a risk to individuals with soy allergies who may not be aware of its presence. Read more at govinfonow.com/recall/22575-le-petit-outre-whole-wheat-bread-recall-undeclared-soy.
Source Summary by GovInfoNow · govinfonow.com/recall/22575-le-petit-outre-whole-wheat-bread-recall-undeclared-soy · Updated October 11, 2026 · FDA enforcement record: FDA #F-1254-2017
Cite this page
“Le Petit Outre Whole Wheat Bread Recall: Undeclared Soy.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/22575-le-petit-outre-whole-wheat-bread-recall-undeclared-soy. Based on FDA recall #F-1254-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1254-2017%22&limit=1).
Why it’s dangerous
The bread contains undeclared soy lecithin, which is an allergen. People with soy allergies could experience a serious allergic reaction if they consume the product without knowing it contains soy.
Who’s affected
Consumers in Montana who purchased 32 oz loaves of Whole Wheat Bread with UPC 6 36428 50200 2 and pull dates of 12/15 or 12/16. Individuals with soy allergies are at risk of an allergic reaction.
How to tell if you have this one
Check for Whole Wheat Bread loaves with a net weight of 32 oz and UPC code 6 36428 50200 2. Verify the pull date on the packaging is either 12/15 or 12/16.
- Brand
Le Petit Outre- Product
Whole Wheat Bread, each loaf has a net wt. 32 oz.. The UPC is code 6 36428 50200 2- Category
Food
All 7 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Terminated- Distribution
distributed in MT only
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| F-1253-2017 | Birdman Bread, each loaf has net wt. 24 oz and 32 oz.. The UPC code ia 6 36428 10200 4.; Pull by date of 12/15, 12/16, 12/17, and 12/18. | 417 units total |
| F-1254-2017 | Whole Wheat Bread, each loaf has a net wt. 32 oz.. The UPC is code 6 36428 50200 2.; Pull by date of 12/15 and 12/16 | 103 units |
| F-1255-2017 | Daily Wheat Bread, each loaf has a net wt. 24 oz.. The UPC is code and 6 36428 50500 3.; Pull by date of 12/15, 12/16, 12/17, and 12/18. | 24 units |
| F-1256-2017 | Italian Deli Loaf, each loaf has a net wt. 32 oz.. The UPC is code 6 36428 50200 2.; Pull by date of 12/15 and 12/16. | 72 units |
| F-1257-2017 | Sourdough Deli Loaf, each loaf has a net wt. 28 oz.. The UPC is code 6 36428 50200 2; Pull by date of 12/15 and 12/16. | 165 units |
| F-1258-2017 | Brewers Grain Deli Loaf, each loaf has a net wt. 24 oz.. The UPC code is 6 36428 10300 1.; Pull by date of 12/15, 12/16, 12/17, and 12/18. | 55 units |
| F-1259-2017 | NY Rye Deli Loaf, each loaf has a net wt. 32 oz.. No UPC as this is for food service only.; Pull by date of 12/15 and 12/16 | 89 units |
What to do — step by step
Stop consuming the bread
Do not eat the recalled Whole Wheat Bread loaves due to the undeclared soy allergen.
Discard or return the product
The recall record does not specify a specific remedy such as a refund or replacement, so consumers should dispose of the product safely.
Where it went and when
Where it was distributed
Distributed in Montana.
FDA distribution: “distributed in MT only” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Montana.
Recall timeline
FDA terminated this recall 57 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
Questions people ask
Where was this product sold?
The affected units were distributed only in Montana.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #F-1254-2017 (December 14, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1254-2017 to see it in context.
- Plain-language summary written by qwen3.6:35b-a3b on October 11, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.