FDA Recall United States TerminatedTerminated: August 17, 2018Historical recordClass II
purely elizabeth.
- Product
- Chocolate Sea Salt Probiotic Granola, Purely Elizabeth, 8oz,…
- Published
- May 9, 2018
- Distribution
- Nationwide
purely elizabeth. Recall: Undeclared Walnut Allergen. Maple Walnut Probiotic granola was packaged in Chocolate Sea Salt probiotic granola bags. - F-0499-2020
United States
TerminatedClass II
- Company
- purely elizabeth.
- Product
- purely elizabeth Chocolate Sea Salt probiotic granola. Net…
- Recall date
- January 2, 2020
- Terminated
- August 16, 2021
- Source
- FDA
Reason for recall
Undeclared Walnut Allergen. Maple Walnut Probiotic granola was packaged in Chocolate Sea Salt probiotic granola bags.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| purely elizabeth Chocolate Sea Salt probiotic granola. Net Wt. 8 oz (227g). UPC 55140-00268. Made with organic quinoa, amaranth and chia. Contains Coconut. May contain Walnuts, Cashews and Almonds. Made in a facility that also processes soy, milk, eggs, peanuts and other tree nuts. | 55140-00268 | 3,719 cases (6 units per case) total | Lot: OH29519 / Best By: 10/21/2020 |
Distribution
- IL
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0499-2020
- Event ID
- 84613
- Status
- Terminated
- Classification
- Class II
- Company
- purely elizabeth.
- Product description
- purely elizabeth Chocolate Sea Salt probiotic granola. Net Wt. 8 oz (227g). UPC 55140-00268. Made with organic quinoa, amaranth and chia. Contains Coconut. May contain Walnuts, Cashews and Almonds. Made in a facility that also processes soy, milk, eggs, peanuts and other tree nuts.
- Quantity
- 3,719 cases (6 units per case) total
- Reason
- Undeclared Walnut Allergen. Maple Walnut Probiotic granola was packaged in Chocolate Sea Salt probiotic granola bags.
- Recall initiation date
- January 2, 2020
- Report date
- January 15, 2020
- Classification date
- Not published in this source record
- Termination date
- August 16, 2021
- Distribution pattern
- IL
- UPC, lot, and code information
- UPC 55140-00268; Lot: OH29519 / Best By: 10/21/2020
- 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: purely elizabeth.
Other recalls from purely elizabeth.
FDA Recall United States TerminatedTerminated: May 8, 2017Historical recordClass II
purely elizabeth.
- Product
- Chocolate Sea Salt Probiotic Granola, Purely Elizabeth, 8oz,…
- Published
- December 7, 2016
- Distribution
- Nationwide
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.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.
New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.
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?
FDA classifies this recall as Class II. See how to read an FDA recall record (linked above) for what each classification level means.
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 responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.
Official guidance and record verification
Public Health Trace does not provide medical advice -- review the linked official source below for current, authoritative information.
How to interpret this historical record
This record is preserved as published by FDA, as of August 16, 2021.
Status as reported: Terminated.
This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.
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.