FDA Recall United States Terminated Historical recordClass II
Drews LLC
- Product
- SimplyNature Organic Chipotle Ranch Dressing, Net Wt. 12 FL…
- Published
- September 21, 2016
- Distribution
- Multiple states
Drews LLC Recall: Undeclared milk and egg allergen.
United States
TerminatedClass I
- Company
- Drews LLC
- Product
- Field Day Organic Ranch Dressing packaged in an 8 fl. oz. gl…
- Recall date
- September 14, 2016
- Terminated
- August 15, 2017
- Source
- FDA
Reason for recall
Undeclared milk and egg allergen.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Field Day Organic Ranch Dressing packaged in an 8 fl. oz. glass bottle, UPC #042563600242. The lot code is located on the back of the bottle above the label. Specifically, the front label of the affected product is correctly labeled Field Day Organic Ranch Dressing, 8 fl oz. The issue is some bottles have an incorrect back label such that the contains statement does not list milk and egg as allergens. These bottles can be identified by UPC# 042563600259. | Not published in this source record | N/A | Lot Code W210I, Best By date of Jan. 28, 2018 |
Distribution
- IL
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0677-2017
- Event ID
- 75176
- Status
- Terminated
- Classification
- Class I
- Company
- Drews LLC
- Product description
- Field Day Organic Ranch Dressing packaged in an 8 fl. oz. glass bottle, UPC #042563600242. The lot code is located on the back of the bottle above the label. Specifically, the front label of the affected product is correctly labeled Field Day Organic Ranch Dressing, 8 fl oz. The issue is some bottles have an incorrect back label such that the contains statement does not list milk and egg as allergens. These bottles can be identified by UPC# 042563600259.
- Quantity
- N/A
- Reason
- Undeclared milk and egg allergen.
- Recall initiation date
- September 14, 2016
- Report date
- December 14, 2016
- Classification date
- Not published in this source record
- Termination date
- August 15, 2017
- Distribution pattern
- IL
- UPC, lot, and code information
- Lot Code W210I, Best By date of Jan. 28, 2018
- 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
Responsible company: Drews LLC
Other recalls from Drews 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 |
|---|---|
| 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?
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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