Kroger recalls Cranberry Orange Bread: Allergy label missing pecans
Kroger recalls Cranberry Orange Bread (16oz) due to missing tree nut allergy warning. Check UPC 864934000044 for affected items sold June 2017 or earlier.
Lower-risk recall
The firm was notified by a customer that the label does not include Pecans or Tree Nuts in the Allergy contain statement.
Contact the company
What happened, in plain English
Kroger recalled Cranberry Orange Bread because it doesn't list tree nuts or pecans on its allergy label. This could cause allergic reactions in people sensitive to these ingredients. Read more at govinfonow.com/recall/21143-kroger-recalls-cranberry-orange-bread-allergy-label-missing-pecans.
Source Summary by GovInfoNow · govinfonow.com/recall/21143-kroger-recalls-cranberry-orange-bread-allergy-label-missing-pecans · Updated October 8, 2026 · FDA enforcement record: FDA #F-2411-2017
Cite this page
“Kroger recalls Cranberry Orange Bread: Allergy label missing pecans.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/21143-kroger-recalls-cranberry-orange-bread-allergy-label-missing-pecans. Based on FDA recall #F-2411-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2411-2017%22&limit=1).
Why it’s dangerous
The bread's allergy label does not include tree nuts or pecans, which could cause allergic reactions in sensitive individuals. This is a labeling issue, not a physical hazard.
Who’s affected
People with tree nut or pecan allergies who ate this bread may experience reactions. Those who bought the product before June 2017 are most at risk.
How to tell if you have this one
Check for the UPC 864934000044 on the bread box. Products sold before June 7, 2017 are affected.
- Brand
Bakehouse Bread- Product
BAKEHOUSE BREAD ARTISAN CRANBERRY ORANGE BREAD, 16 OZ UPC 8 64934 00004 4 Bakehouse Bread Company Tucson, AZ- Category
Food
What to do — step by step
Check Label
Look for the allergy label that should list tree nuts or pecans.
Where it went and when
Where it was distributed
Distributed in Arizona.
FDA distribution: “Product was sold in Arizona” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Arizona.
Recall timeline
FDA terminated this recall 7 months after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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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-2411-2017 (June 2, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2411-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 8, 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.