CLASS II Food recall · Reported 25 Jan 2017 · FDA Enforcement Report
NY Rye Deli Loaf, each loaf recalled by Great Northern Bakehouse
Great Northern Bakehouse is recalling NY Rye Deli Loaf, each loaf has a, distributed in Montana. The recall was initiated on 14 Dec 2016 and the FDA has classified it as Class II.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-1259-2017
- FDA event ID
- 75958
- Recalling firm
- Great Northern Bakehouse, Missoula, MT
- Brand
- NY Rye
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 14 Dec 2016
- FDA classified
- 13 Jan 2017
- Reported
- 25 Jan 2017
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Undeclared Soy
- Product category
- Other
Timeline
| 14 Dec 2016 | Recall initiated by company | |
| 13 Jan 2017 | Classified by FDA | +30 days |
| 25 Jan 2017 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
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.
Product as listed by the FDA
NY Rye Deli Loaf, each loaf has a net wt. 32 oz.. No UPC as this is for food service only.
Where it was distributed
distributed in MT only
Questions about this recall
Why was it 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 lots are affected?
Pull by date of 12/15 and 12/16
Where was it sold?
distributed in MT only
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
6 other products · FDA event 75958This product is part of a recall event; the main page for the event is Whole Wheat Bread, each loaf recalled by Great Northern Bakehouse.
More recalls from Great Northern Bakehouse
All 7| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Food | CLASS II | Daily Wheat Bread, each loaf recalled by Great Northern BakehouseDaily | Great Northern Bakehouse | Undeclared Soy | MT |
| Food | CLASS II | Brewers Grain Deli Loaf, each loaf recalled by Great Northern BakehouseBrewers Grain | Great Northern Bakehouse | Undeclared Soy | MT |
| Food | CLASS II | Sourdough Deli Loaf, each loaf recalled by Great Northern Bakehouse | Great Northern Bakehouse | Undeclared Soy | MT |
| Food | CLASS II | Italian Deli Loaf, each loaf recalled by Great Northern Bakehouse | Great Northern Bakehouse | Undeclared Soy | MT |
| Food | CLASS II | Birdman Bread, each loaf recalled by Great Northern BakehouseBirdman | Great Northern Bakehouse | Undeclared Soy | MT |
Other Other recalls
All 4,664| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Food | CLASS I | Alfalfa, Net Weight 50 lbs. bag, Product of USA, International recalledAlfalfa | International Sprout Holdings | Salmonella | 17 states |
| Food | CLASS I | Crown Farms Dried Suri Cut, 200 gm per, keep frozen recalledCrown | Euro Foods Group USA NJ | Foreign Material | 4 states |
| Food | CLASS I | Item # DIPPIC0205RFS Pico de Gallo 5 lb packaged in round plastic recalledItem | Ron's Home Style Foods | Salmonella | AR, OK, TX |
| Food | CLASS I | Food to Live Organic SuperGrass Powder recalled by Lexunder | Lexunder | Salmonella | 40 states |
| Food | ANNOUNCED | Epinephrine Injection, USP 30 mg/ (1 mg/mL) multi dose vial recalledAmerican Regent, Inc. | American Regent | Particulate Matter | Nationwide |