FDA Recall United States Terminated Historical recordClass II
Arro Corporation
- Product
- Caramel Apple Cake Mix (590g)
- Published
- February 8, 2017
- Distribution
- MN, IN, WA, Canada
Arro Corporation Recall: Possible contamination of product with Salmonella due to incorporation of powdered milk and powdered buttermilk .
United States
TerminatedClass II
- Company
- Arro Corporation
- Product
- Hot Cocoa, NOT FOR RETAIL SALE, Prod: 28OCT2016, BB: 28JUN20…
- Recall date
- December 13, 2016
- Terminated
- April 15, 2019
- Source
- FDA
Reason for recall
Possible contamination of product with Salmonella due to incorporation of powdered milk and powdered buttermilk .
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Hot Cocoa, NOT FOR RETAIL SALE, Prod: 28OCT2016, BB: 28JUN2017, Net Weight: 907 g (2.0 lb), Best Before: 28JUN2017 | Not published in this source record | 46 cases (6 pouches per case) | Lot: AR63028 |
Distribution
- MN
- IN
- WA
- Canada
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1376-2017
- Event ID
- 75946
- Status
- Terminated
- Classification
- Class II
- Company
- Arro Corporation
- Product description
- Hot Cocoa, NOT FOR RETAIL SALE, Prod: 28OCT2016, BB: 28JUN2017, Net Weight: 907 g (2.0 lb), Best Before: 28JUN2017
- Quantity
- 46 cases (6 pouches per case)
- Reason
- Possible contamination of product with Salmonella due to incorporation of powdered milk and powdered buttermilk .
- Recall initiation date
- December 13, 2016
- Report date
- February 8, 2017
- Classification date
- Not published in this source record
- Termination date
- April 15, 2019
- Distribution pattern
- MN, IN, WA, Canada
- UPC, lot, and code information
- Lot: AR63028
- 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
Other products recalled under this same event
This recall shares FDA event ID 75946 with 2 other product entries in Public Health Trace.
FDA Recall United States Terminated Historical recordClass II
Arro Corporation
- Product
- 50423 Madison Hot Cocoa WIP; Production date 11/30/16
- Published
- February 8, 2017
- Distribution
- MN, IN, WA, Canada
Responsible company: Arro Corporation
Other recalls from Arro Corporation
FDA Recall United States Terminated Historical recordClass II
Arro Corporation
- Product
- 10.0 Grams Chili Spice Blend in packets
- Published
- May 10, 2017
- Distribution
- OH
FDA Recall United States Terminated Historical recordClass II
Arro Corporation
- Product
- Caramel Apple Cake Mix (590g)
- Published
- February 8, 2017
- Distribution
- MN, IN, WA, Canada
FDA Recall United States Terminated Historical recordClass II
Arro Corporation
- Product
- 50423 Madison Hot Cocoa WIP; Production date 11/30/16
- Published
- February 8, 2017
- Distribution
- MN, IN, WA, Canada
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 |
|---|---|
| Minnesota | 1 |
| Indiana | 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.
