Severity
Moderate
ModerateClass IITerminated
FDA Food recall · Reported January 25, 2017
NY Rye Deli Loaf, each loaf has a net wt. 32 oz.. No UPC as this is for food service only.
NY Rye Deli Loaf 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.
Great Northern Bakehouse Inc. dba Le Petit Outre recalled NY Rye Deli Loaf, each loaf has a net wt. 32 oz.. No UPC as this is for food service only. - a moderate-severity action.
NY Rye Deli Loaf, each loaf has a net wt. 32 oz.. No UPC as this is for food service only. was recalled by Great Northern Bakehouse Inc. dba Le Petit Outre in January 25, 2017. Reason: NY Rye Deli Loaf is recalled due to undeclared soy lecithin. The soy allergen is present in DDA pan spray (re…. Check the official notice for the remedy. Verify recall #F-1259-2017 with the FDA Food before acting.
The recall
Great Northern Bakehouse Inc. dba Le Petit Outre issued this moderate-severity FDA Food recall-NY Rye Deli Loaf is recalled due to undeclared soy lecithin. The soy allergen is present in DDA pan spray (re….
- Moderate
- severity level
- 89 units
- affected scope
- Class II
- classification
- January 25, 2017
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-1259-2017 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-1259-2017) was formally reported on January 25, 2017, with the manufacturer initiating the action on December 14, 2016. It is classified under Moderate severity (Class II), with a current status of Terminated. Great Northern Bakehouse Inc. dba Le Petit Outre is listed as the recalling firm, operating out of Missoula, MT. Federal records list the affected scope as 89 units.
The documented reason for this recall is: NY Rye Deli Loaf 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. Distribution data in the federal record shows the product reached: distributed in MT only. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 2 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Food recalls over time
Where this recall sits in its category - 25,126 food recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
89 units
Related Recalls
6
2 from same agency
Product description
NY Rye Deli Loaf, each loaf has a net wt. 32 oz.. No UPC as this is for food service only.
Reason for recall
NY Rye Deli Loaf 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.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-1259-2017 |
| Date reported | January 25, 2017 |
| Date initiated | December 14, 2016 |
| Recalling firm | Great Northern Bakehouse Inc. dba Le Petit Outre |
| Firm location | Missoula, MT |
| Affected scope | 89 units |
| Distribution | distributed in MT only |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (F-1259-2017) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
NY Rye Deli Loaf, each loaf has a net wt. 32 oz.. No UPC as this is for food service only.. Recalled by Great Northern Bakehouse Inc. dba Le Petit Outre. Units affected: 89 units.
Why was this product recalled? ▼
NY Rye Deli Loaf 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.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on January 25, 2017. Severity: Moderate. Recall number: F-1259-2017.
Where was the recalled product distributed? ▼
Distribution: distributed in MT only.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-1259-2017) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported January 25, 2017. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.