Food Gusto, Inc. Recall: Birdy 3 in 1 Coffee Mix (Robusta) may contain undeclared milk allergen and the nutritional labeling is unclear.
United States
TerminatedClass I
- Company
- Food Gusto, Inc.
- Product
- Birdy 3 in 1 Robusta Coffea Mix, 445.5 g in a red sealed pla…
- Recall date
- May 10, 2016
- Terminated
- December 27, 2016
- Source
- FDA
Reason for recall
Birdy 3 in 1 Coffee Mix (Robusta) may contain undeclared milk allergen and the nutritional labeling is unclear.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Birdy 3 in 1 Robusta Coffea Mix, 445.5 g in a red sealed plastic bag, Product of Thailand, UPC 8850250007425 | 8850250007425 | 30 cartons | Lot #D092121515 |
Distribution
- CT
- MA and NY
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0189-2017
- Event ID
- 74159
- Status
- Terminated
- Classification
- Class I
- Company
- Food Gusto, Inc.
- Product description
- Birdy 3 in 1 Robusta Coffea Mix, 445.5 g in a red sealed plastic bag, Product of Thailand, UPC 8850250007425
- Quantity
- 30 cartons
- Reason
- Birdy 3 in 1 Coffee Mix (Robusta) may contain undeclared milk allergen and the nutritional labeling is unclear.
- Recall initiation date
- May 10, 2016
- Report date
- October 26, 2016
- Classification date
- Not published in this source record
- Termination date
- December 27, 2016
- Distribution pattern
- CT, MA and NY
- UPC, lot, and code information
- UPC 8850250007425; Lot #D092121515
- 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: Food Gusto, 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 |
|---|---|
| Connecticut | 1 |
| Massachusetts | 1 |
| New York | 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?
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.
