Great Northern Bakehouse Inc. dba Le Petit Outre
Complete recall history across all FDA and CPSC categories — 7 total recalls
Great Northern Bakehouse Inc. dba Le Petit Outre appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.
Food Recalls (7)
FDA food safety enforcement actions by Great Northern Bakehouse Inc. dba Le Petit Outre
| Date | Product | Reason | Class |
|---|---|---|---|
| Dec 14, 2016 | NY Rye Deli Loaf, each loaf has a net wt. 32 oz.. No UPC as this is for food ... | NY Rye Deli Loaf is recalled due to undeclared soy lecithin. The soy allergen... | Class II |
| Dec 14, 2016 | Daily Wheat Bread, each loaf has a net wt. 24 oz.. The UPC is code and 6 364... | Daily Wheat Bread is recalled due to undeclared soy lecithin. The soy allerge... | Class II |
| Dec 14, 2016 | Brewers Grain Deli Loaf, each loaf has a net wt. 24 oz.. The UPC code is 6 36... | Brewers Grain Deli Loaf is recalled due to undeclared soy lecithin. The soy a... | Class II |
| Dec 14, 2016 | Sourdough Deli Loaf, each loaf has a net wt. 28 oz.. The UPC is code 6 36428 ... | Sourdough Deli Loaf is recalled due to undeclared soy lecithin. The soy aller... | Class II |
| Dec 14, 2016 | Italian Deli Loaf, each loaf has a net wt. 32 oz.. The UPC is code 6 36428 5... | Italian Deli Loaf is recalled due to undeclared soy lecithin. The soy allerge... | Class II |
| Dec 14, 2016 | Birdman Bread, each loaf has net wt. 24 oz and 32 oz.. The UPC code ia 6 3642... | Birdman Bread is recalled due to undeclared soy lecithin. The soy allergen is... | Class II |
| Dec 14, 2016 | Whole Wheat Bread, each loaf has a net wt. 32 oz.. The UPC is code 6 36428 50... | Whole Wheat Bread is recalled due to undeclared soy lecithin. The soy allerge... | Class II |
Frequently Asked Questions
A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.
Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.
The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.
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