Two Moms in the Raw, Gluten-Free Pesto Sea Cracker enclosed in brown semi-synthetic packaging with a transparent section displaying the c...
⚠ 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.
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1991-2012.
Two Moms in the Raw is issuing a voluntary recall for Pesto Sea Cracker, 4 oz, because they were notified by their raw material supplier that the pine nuts used in the product may contain peanuts.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1991-2012.
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 2 Moms In The Raw, Llc 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-1991-2012.
2 Moms in the Raw, LLC
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.
2 Moms In The Raw, Llc Recall FAQ
2 Moms In The Raw, Llc is the subject of a bakery & grains safety report: Two Moms in the Raw, Gluten-Free Pesto Sea Cracker enclosed in brown semi-synthetic packaging with a transparent section displaying the c.... The notice was published on August 7, 2012 by the U.S. Food and Drug Administration (FDA). Approximately 4,618 units are potentially affected.