FDA Recall United States Terminated Historical recordClass II
Bob's Red Mill Natural Foods, Inc.
- Product
- Organic Amaranth Grain Gluten Free, Bob's Red Mill brand, pa…
- Published
- August 31, 2022
- Distribution
- Distributed in CA, CT, FL, GA, IL, IN, K…
Bob's Red Mill Natural Foods, Inc. Recall: The firm is voluntarily recalling one lot of Guar Gum due to due to the inclusion of a misidentified ingredient, hydroxyethylcellulose.
United States
TerminatedClass III
- Company
- Bob's Red Mill Natural Foods, Inc.
- Product
- Label reads in part "*** Bob's Red Mill *** PREMIUM GUAR GUM…
- Recall date
- September 24, 2016
- Terminated
- November 4, 2016
- Source
- FDA
Reason for recall
The firm is voluntarily recalling one lot of Guar Gum due to due to the inclusion of a misidentified ingredient, hydroxyethylcellulose.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Label reads in part "*** Bob's Red Mill *** PREMIUM GUAR GUM SUPERB GLUTEN FREE THICKENER & BINDER *** NET WT 8 OZ ***" Product is packaged in multilayered flexible film with multiple colors. Firm brand name is printed in red. Case contains 8/8 oz. packages. UPC 0 39978 00554 0 or 0 39978 00554 1 | Not published in this source record | 443 cs | Cases for US - Item # 1598C088; lot 212463; Best By: 7/18/2018, GTIN # 30039978005541, UPC 039978005540. Cases for Canada - Item # 1598C226G8CA; lot 213189, Best By: 7/18/2018, GTIN # 30039978305542, UPC 039978005541. |
Distribution
- Nationwide and Canada
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0281-2017
- Event ID
- 75307
- Status
- Terminated
- Classification
- Class III
- Company
- Bob's Red Mill Natural Foods, Inc.
- Product description
- Label reads in part "*** Bob's Red Mill *** PREMIUM GUAR GUM SUPERB GLUTEN FREE THICKENER & BINDER *** NET WT 8 OZ ***" Product is packaged in multilayered flexible film with multiple colors. Firm brand name is printed in red. Case contains 8/8 oz. packages. UPC 0 39978 00554 0 or 0 39978 00554 1
- Quantity
- 443 cs
- Reason
- The firm is voluntarily recalling one lot of Guar Gum due to due to the inclusion of a misidentified ingredient, hydroxyethylcellulose.
- Recall initiation date
- September 24, 2016
- Report date
- November 2, 2016
- Classification date
- Not published in this source record
- Termination date
- November 4, 2016
- Distribution pattern
- Nationwide and Canada
- UPC, lot, and code information
- Cases for US - Item # 1598C088; lot 212463; Best By: 7/18/2018, GTIN # 30039978005541, UPC 039978005540. Cases for Canada - Item # 1598C226G8CA; lot 213189, Best By: 7/18/2018, GTIN # 30039978305542, UPC 039978005541.
- 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: Bob's Red Mill Natural Foods, Inc.
Other recalls from Bob's Red Mill Natural Foods, Inc.
FDA Recall United States Terminated Historical recordClass III
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- Published
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- Distribution
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FDA Recall United States Terminated Historical recordClass III
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- Product
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- Published
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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 III mean?
A situation in which use of or exposure to a product is not likely to cause adverse health consequences.
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?
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