JCB FLAVORS, LLC, Product Code 8102920812, 8102923212, 8102921606, Chili Powder #810292 , 12 x 8oz jar, UPC: 66049244520, 66049244506.
⚠ 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-2115-2015.
JCB Flavors is conducting a recall on various Seasonings which used ground cumin as an ingredient received in Oct - Dec 2014. JCB Flavors was informed by their supplier of ground cumin, Schiff Food Products, that the product tested positive for trace amounts of peanut allergens.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2115-2015.
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 Jcb Flavors, 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-2115-2015.
JCB Flavors, 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.
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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.
Jcb Flavors, Llc Recall FAQ
Jcb Flavors, Llc is the subject of a food safety report: JCB FLAVORS, LLC, Product Code 8102920812, 8102923212, 8102921606, Chili Powder #810292 , 12 x 8oz jar, UPC: 66049244520, 66049244506.. The notice was published on January 8, 2015 by the U.S. Food and Drug Administration (FDA). Approximately 1,040 units are potentially affected.