FDA recall record

JCB Flavors LLC, Product Code 1002660812, Chipotle Chili&Garlic Dip recall — FDA F-2117-2015

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…

Class IIclassification
F-2117-2015official record ID
May 6, 2015report date

Recall record at a glance

Official recordF-2117-2015
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmJCB Flavors, LLC
Report dateMay 6, 2015
Recall initiation dateJan 8, 2015
Quantity1040 lbs total from all products.
LocationSullivan, WI, United States

Official product description

JCB FLAVORS, LLC, Product Code 1002660812, Chipotle Chili&Garlic Dip #100266 , 12 x 5.5oz jar,1 oz pouch.

Why the product was recalled

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.

Distribution information

WI, IL, MN, CA, IN, NJ, AR.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.