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CriticalFDAfda-F-0934-2018UNDECLARED ALLERGEN

All-Natural Ciolo Nut-Free Basil Pesto, 7 oz., plastic container, Item #: 30019.18

⚠ 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
504
Recall Date
February 28, 2018
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0934-2018.

Firm is recalling Nut-Free Basil Pesto due to mislabeling, causing undeclared tree nuts.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0934-2018.

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 Blue Moose Of Boulder, 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-0934-2018.

Blue Moose of Boulder, 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.

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📣 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.

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Blue Moose Of Boulder, Llc Recall FAQ

Blue Moose Of Boulder, Llc is the subject of a food safety report: All-Natural Ciolo Nut-Free Basil Pesto, 7 oz., plastic container, Item #: 30019.18. The notice was published on February 28, 2018 by the U.S. Food and Drug Administration (FDA). Approximately 504 units are potentially affected.