Skip to main content
RecallFDAfda-F-2331-2016MISLABELED

EAT Barbeque Zero to Hero, a Sweet Rub, packaged in 6.5oz bottles (mislabeled). The responsible firm named on the label is Pellet Envy, ...

Category
Units Affected
93
Recall Date
June 21, 2016
Issuing Agency
Hazard
Mislabeled

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2331-2016.

Some bottles of barbeque seasoning without a statement noting the product contains MSG (monosodium glutamate).

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2331-2016.

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 Old World Spices & Seasonings Inc 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-2331-2016.

Old World Spices & Seasonings Inc

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

Old World Spices & Seasonings Inc Recall FAQ

Old World Spices & Seasonings Inc is the subject of a food safety report: EAT Barbeque Zero to Hero, a Sweet Rub, packaged in 6.5oz bottles (mislabeled). The responsible firm named on the label is Pellet Envy, .... The notice was published on June 21, 2016 by the U.S. Food and Drug Administration (FDA). Approximately 93 units are potentially affected.