Ideal Protein, Sea Salt & Vinegar Ridges, 7 packets Net WT 1.4 oz (40 g) each. Total net weight 9.9 oz (280 g). Distributed by Laboratori...
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1319-2013.
Dakota Specialty Milling informed Zumbro River Brand (ZRB) that they are recalling Multigrain Whole Meal Flour Blend 100 (Multigrain Flour) because of a potential contamination with fine wire pieces. This Multigrain Flour is a component in an extruded base called Whey multigrain Ridges, so these fine wire pieces could be contained in the Whey Muligrain Ridges. The fine wire is too thin to be det
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1319-2013.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact Zumbro River Brand, Inc or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- If you've been hurt by this product, report the incident to FDA.
Consumer Contact (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1319-2013.
Zumbro River Brand, Inc
About the U.S. Food and Drug Administration
The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.
Visit FDA.gov →📣 Report a food, supplement, or cosmetic problem to the FDA
If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.
Zumbro River Brand, Inc Recall FAQ
Zumbro River Brand, Inc is the subject of a food safety report: Ideal Protein, Sea Salt & Vinegar Ridges, 7 packets Net WT 1.4 oz (40 g) each. Total net weight 9.9 oz (280 g). Distributed by Laboratori.... The notice was published on February 7, 2013 by the U.S. Food and Drug Administration (FDA). Approximately 58,610 units are potentially affected.