Fred Meyer Inc. Recall: 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.
United States
TerminatedClass I
- Company
- Fred Meyer Inc.
- Product
- Product 8x8 " individually packaged in black plastic trays…
- Recall date
- October 14, 2018
- Terminated
- November 14, 2018
- Source
- FDA
Reason for recall
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.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| 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***". | 111110-02100 | 432 Units | Time Stamp (HH/MM) followed by FK 285F |
Distribution
- distributed in OR
- and WA
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0371-2019
- Event ID
- 81288
- Status
- Terminated
- Classification
- Class I
- Company
- Fred Meyer Inc.
- Product description
- 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
- Reason
- 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.
- Recall initiation date
- October 14, 2018
- Report date
- November 14, 2018
- Classification date
- Not published in this source record
- Termination date
- November 14, 2018
- Distribution pattern
- distributed in OR, and WA
- UPC, lot, and code information
- UPC 111110-02100; Time Stamp (HH/MM) followed by FK 285F
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Fred Meyer Inc.
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Oregon | 1 |
| Washington | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class I mean?
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
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