FDA recall record

C.J. Dannemiller Company The sunflower kernels roasted recall — FDA F-1698-2016

Firm recalling under directions from their Supplier, due to possible risk of product containing Listera monocytogenes.

Class Iclassification
F-1698-2016official record ID
Jul 27, 2016report date

Recall record at a glance

Official recordF-1698-2016
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmC.J. Dannemiller Company, Inc.
Report dateJul 27, 2016
Recall initiation dateMay 20, 2016
Quantity823 boxes /30 lbs cases SALTED and 253 boxes/30 lbs cases NO SALT
LocationNorton, OH, United States

Official product description

The sunflower kernels roasted ( no salt) were packed in a 30 lbs. corrugated box with a poly liner with the following labeling: 1. Roasted and No salt 30 lbs brown cardboard box labeled "SUNFLOWER KRNLS", "INGREDIENTS: Sunflower Kernels, Peanut Oil." "NET WT. 30 LBS. (13.61 KG.)" ; "CJ DANNEMILLER CO., NORTON, OHIO 44203" ; "CLEVELAND KOSHER" and UPC "113671020922". 2. Roasted and No salt 30 lbs brown cardboard box with private labeling labeled "SUNFLOWER KRNLS", "INGREDIENTS: Sunflower Kernels, Peanut Oil." "NET WT. 30 LBS. (13.61 KG.)" ; and UPC "113671020922"

Why the product was recalled

Firm recalling under directions from their Supplier, due to possible risk of product containing Listera monocytogenes.

Distribution information

AR, CO, FL, IA, IN, KY, MI, NY, OH, PA, SD, VA, WI and WV.

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement 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.