PAO DE MILHO III, LLC Recall: Brioche Donuts- Bavarian Cream contain undeclared FD&C yellow #5 and FD&C yellow #6.
United States
TerminatedClass II
- Company
- PAO DE MILHO III, LLC
- Product
- Triana Family Brioche Donuts Bavarian Cream Net Wt. 0.75 LBS…
- Recall date
- August 30, 2016
- Terminated
- March 14, 2017
- Source
- FDA
Reason for recall
Brioche Donuts- Bavarian Cream contain undeclared FD&C yellow #5 and FD&C yellow #6.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Triana Family Brioche Donuts Bavarian Cream Net Wt. 0.75 LBS (340 g) 12 -24 Jabez St., Newark, NJ 07106 UPC 000260003995 packaged in a clear plastic clam shell container | 000260003995 | 60 units | 9/13/2016 |
Distribution
- NJ
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-2620-2016
- Event ID
- 75185
- Status
- Terminated
- Classification
- Class II
- Company
- PAO DE MILHO III, LLC
- Product description
- Triana Family Brioche Donuts Bavarian Cream Net Wt. 0.75 LBS (340 g) 12 -24 Jabez St., Newark, NJ 07106 UPC 000260003995 packaged in a clear plastic clam shell container
- Quantity
- 60 units
- Reason
- Brioche Donuts- Bavarian Cream contain undeclared FD&C yellow #5 and FD&C yellow #6.
- Recall initiation date
- August 30, 2016
- Report date
- October 5, 2016
- Classification date
- Not published in this source record
- Termination date
- March 14, 2017
- Distribution pattern
- NJ
- UPC, lot, and code information
- UPC 000260003995; 9/13/2016
- 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: PAO DE MILHO III, LLC
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 |
|---|---|
| New Jersey | 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.
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