FDA Recall United States Terminated Historical recordClass II
E & E Enterprises
- Product
- Cheesey Bacon Dip, Muriel's brand, dry mix, packaged in 1 pi…
- Published
- November 15, 2017
- Distribution
- distributed in CO, MI, and WA.
E & E Enterprises Recall: Ingredients statement declared whey, powdered cheese and cheddar cheese but did not declare milk. In addition, FD&C colors Yellow #5 and Yellow #6 are not declared.
United States
TerminatedClass II
- Company
- E & E Enterprises
- Product
- Cheesey Pizza Dip, Muriel's brand, dry mix, packaged in 1 pi…
- Recall date
- October 25, 2017
- Terminated
- May 2, 2018
- Source
- FDA
Reason for recall
Ingredients statement declared whey, powdered cheese and cheddar cheese but did not declare milk. In addition, FD&C colors Yellow #5 and Yellow #6 are not declared.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Cheesey Pizza Dip, Muriel's brand, dry mix, packaged in 1 pint glass jar. Cheesey Pizza Dip, Muriel's brand, dry mix, packaged in plastic bag, net wt. 1 oz.. The label is read in parts: "***Ingredients: Onion, Red & Green Peppers, Garlic, Cayenne, Powdered Cheese (Maltodextrin, Tapioca Starch, Whey, Soybean Oil, Salt, Dextrose, Canola Oil, Cheddar Cheese Flavor Blend), Spices***". | Not published in this source record | 2 glass jars and 145 bags | None |
Distribution
- distributed in CO
- MI
- and WA.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0154-2018
- Event ID
- 78425
- Status
- Terminated
- Classification
- Class II
- Company
- E & E Enterprises
- Product description
- Cheesey Pizza Dip, Muriel's brand, dry mix, packaged in 1 pint glass jar. Cheesey Pizza Dip, Muriel's brand, dry mix, packaged in plastic bag, net wt. 1 oz.. The label is read in parts: "***Ingredients: Onion, Red & Green Peppers, Garlic, Cayenne, Powdered Cheese (Maltodextrin, Tapioca Starch, Whey, Soybean Oil, Salt, Dextrose, Canola Oil, Cheddar Cheese Flavor Blend), Spices***".
- Quantity
- 2 glass jars and 145 bags
- Reason
- Ingredients statement declared whey, powdered cheese and cheddar cheese but did not declare milk. In addition, FD&C colors Yellow #5 and Yellow #6 are not declared.
- Recall initiation date
- October 25, 2017
- Report date
- November 15, 2017
- Classification date
- Not published in this source record
- Termination date
- May 2, 2018
- Distribution pattern
- distributed in CO, MI, and WA.
- UPC, lot, and code information
- None
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Other products recalled under this same event
This recall shares FDA event ID 78425 with 1 other product entry in Public Health Trace.
Responsible company: E & E Enterprises
Other recalls from E & E Enterprises
FDA Recall United States Terminated Historical recordClass II
E & E Enterprises
- Product
- Cheesey Bacon Dip, Muriel's brand, dry mix, packaged in 1 pi…
- Published
- November 15, 2017
- Distribution
- distributed in CO, MI, and WA.
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 |
|---|---|
| Colorado | 1 |
| Michigan | 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 II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
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?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
