Recall Register

Food recall: Label reads in part "*** Bob's Red Mill *** PREMIUM GUAR GUM SUPERB GLUTEN FREE THICKENER & BINDER *** NET WT 8 OZ…

Class III FDA enforcement event 75307. Recall start date: . Status in the FDA record: Terminated. Termination date: .

Reason for recall, in the words of FDA

The firm is voluntarily recalling one lot of Guar Gum due to due to the inclusion of a misidentified ingredient, hydroxyethylcellulose.

Class III, in the words of FDA

a situation in which use of or exposure to a violative product is not likely to cause adverse health consequences

Bob's Red Mill Natural Foods, Inc. started this food recall on 24 Sep 2016. The firm address in the FDA record is in Milwaukie, OR. FDA put the recall in Class III. FDA event 75307 has 1 product record. The first FDA enforcement report date is 2 Nov 2016. The record gives the status Terminated, with the termination date 4 Nov 2016.

It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.

FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .

Distribution

In the words of FDA.

Nationwide and Canada

Recalling firm

Bob's Red Mill Natural Foods, Inc., Milwaukie, OR.

Recalling firm: The firm that the FDA record names for a recall.

FDA records how the recall started: Voluntary: Firm initiated.

Products

1 product record in the event.

FDA event 75307: product records
Recall numberProductQuantityClassStatusReport date
F-0281-2017Label 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 1443 csClass IIITerminated2 Nov 2016

openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports. Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.

Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.

Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.

Class III: The lowest of the three FDA recall classes.

The event in context

Food events that started in 2016
799
Share of these events in Class III
5%
Product records in this event
1Median of the firm: 1
Events of the firm on the register
7

Other events of the firm

Official channels

Cite this page

Recall Register. FDA enforcement event 75307. https://recallregister.com/fda/iii/75307/. Source: openFDA enforcement reports. Data through .

Sources

Source
openFDA food enforcement reports
Licence
CC0 1.0
Export date
28 Sep 2026
Newest FDA report date on the register
23 Sep 2026

FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.

Questions

Where was the product distributed?
The FDA record gives this distribution: Nationwide and Canada
What quantity of product is in FDA event 75307?
The FDA record gives this quantity: 443 cs
How did the recall start?
The FDA record says: Voluntary: Firm initiated
How many food recalls of 2016 have the same class?
5% of the 799 food events that started in 2016 are in Class III.