Product 8x8 " individually packaged in black plastic trays with… recall
Recalled by Fred Meyer Inc. · Clackamas, OR, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Angel Food Cake Bar was recalled due to undeclared milk and soy. The actual product inside container is corn breads and it was mislabeled as Angel Food Cake Bar.
Undeclared allergens: Milk Soy
For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.
What was recalled
Product 8x8 " individually packaged in black plastic trays with clear plastic dome lid is cornbread and it was MIS-LABELED as Angel Food Cake Bar. The label of Angel Food Cake Bar has the UPC 111110-02100. The label is read in parts: "***Angel Food Cake Bar *** Net wt. 12 oz *** Contains: Wheat and Eggs *** Distributed by Inter-American Products, Inc. Cincinnati, OH 45202***".
Quantity: 432 Units
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.
Time Stamp (HH/MM) followed by FK 285F
Where it was sold
Oregon Washington
FDA's distribution note: distributed in OR, and WA
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to milk, soy; for anyone else the product is generally not a safety concern. 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
- Fred Meyer Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Oct 14, 2018
- In FDA report of
- Nov 14, 2018
- Terminated
- Nov 14, 2018
- FDA recall number
- F-0371-2019 · event 81288
- Official record
- FDA enforcement report search