FDA Recall United States Terminated Historical recordClass II
Puratos Corporation
- Product
- Tegral Satin EC CL Vegan Cake packaged in 50lbs bags
- Published
- February 3, 2021
- Distribution
- Distributed to a distributor in NY who s…
Puratos Corporation Recall: Product contains undeclared milk.
United States
TerminatedClass I
- Company
- Puratos Corporation
- Product
- Tegral Satin Gold CL Cr¿me Cake, packaged in 50 lb. bag.
- Recall date
- January 16, 2019
- Terminated
- March 14, 2023
- Source
- FDA
Reason for recall
Product contains undeclared milk.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Tegral Satin Gold CL Cr¿me Cake, packaged in 50 lb. bag. | Not published in this source record | 25,700 lbs | 0003486361, 0003532889, 0003532890, 0003532891, 003570383, 0003701561, 0003833985 |
Distribution
- Product was distributed in FL
- OH
- SC
- TX
- PA
- MD
- MA
- MN
- and IL.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1057-2019
- Event ID
- 81947
- Status
- Terminated
- Classification
- Class I
- Company
- Puratos Corporation
- Product description
- Tegral Satin Gold CL Cr¿me Cake, packaged in 50 lb. bag.
- Quantity
- 25,700 lbs
- Reason
- Product contains undeclared milk.
- Recall initiation date
- January 16, 2019
- Report date
- March 6, 2019
- Classification date
- Not published in this source record
- Termination date
- March 14, 2023
- Distribution pattern
- Product was distributed in FL, OH, SC, TX, PA, MD, MA, MN, and IL.
- UPC, lot, and code information
- 0003486361, 0003532889, 0003532890, 0003532891, 003570383, 0003701561, 0003833985
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Telephone
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Puratos Corporation
Other recalls from Puratos Corporation
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 |
|---|---|
| Florida | 1 |
| Ohio | 1 |
| South Carolina | 1 |
| Texas | 1 |
| Pennsylvania | 1 |
| Maryland | 1 |
| Massachusetts | 1 |
| Minnesota | 1 |
| Illinois | 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?
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?
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