Momchipz Gluten Free Veggie Chips Broccoli Florets & Cauliflower
Reason Undeclared Wheat.
Village Baker SPECIALTY ARTISAN BREADS CINNAMON CHIP SOURDOUGH recall
Recalled by Artisan Baking Company, LLC. · Ashland, OR, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Cinnamon Chip Sourdough Village Baker brand was recalled because the label does not declare sub ingredients milk powder and soy lecithin.
A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.
What was recalled
Village Baker SPECIALTY ARTISAN BREADS CINNAMON CHIP SOURDOUGH. The product is whole sliced loaves packed in clear plastic bags that are closed with a twist tie. The net weight is 1.5 lbs. The loaves were sold as individual units. The UPC is 6 42739 00121 9. The product's label is read in parts: "***CINNAMON CHIP SOURDOUGH ***Unbleached wheat flour, barley flour, (ascorbic acid, niacin, iron, thiamine, mononitrate, folic acid, riboflavin, enzyme), water, levain, cinnamon chips, sea salt***All Natural Yeast Free No Preservatives Contains Cornmeal***".
Quantity: 6 loaves
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
09-22 and 09-23. The codes are printed on a white adhesive label on the bottom of the loaf.
Where it was sold
Oregon
FDA's distribution note: distributed in OR
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Artisan Baking Company, LLC.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Sep 20, 2018
- In FDA report of
- Nov 14, 2018
- Terminated
- Nov 6, 2018
- FDA recall number
- F-0370-2019 · event 81078
- Official record
- FDA enforcement report search
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