Skip to main content
CriticalFDAfda-F-1571-2016UNDECLARED ALLERGEN

Pea protein 85% dry powder in a 20 KG bag.

⚠ Critical Alert — Stop Using Immediately

This product has been flagged with severe risks (undeclared allergen). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.

Category
Units Affected
3,700
Recall Date
October 16, 2015
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1571-2016.

Undeclared Soy on label. RFR was generated by a customer who used the Pea Protein in a blended product that claims to be soy free. The Pea Protein tested positive for soy allergen.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1571-2016.

Recall terminated by FDA.

✅ What you should do

  1. Stop using the product if you own it.
  2. Check the model number, lot code, or sell-by date against the recall notice above.
  3. Contact Prinova Us Llc or the retailer where you bought it for a refund, replacement, or repair.
  4. For the most current official instructions, visit the FDA recall page.
  5. 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-1571-2016.

Prinova US LLC

FDA

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.

How to report to FDAFile a report at FDA

Prinova Us Llc Recall FAQ

Prinova Us Llc is the subject of a food safety report: Pea protein 85% dry powder in a 20 KG bag.. The notice was published on October 16, 2015 by the U.S. Food and Drug Administration (FDA). Approximately 3,700 units are potentially affected.