Recall record at a glance
| Official record | F-0314-2017 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Ohio Hickory Harvest Brand Products Inc. |
| Report date | Dec 21, 2016 |
| Recall initiation date | May 4, 2016 |
| Quantity | 4,642 Cases (various size and quantities per case) + 8/50 lb bags |
| Location | Akron, OH, United States |
Official product description
Roasted & Salted Sunflower Kernels under the following brand names: AMISH FARMS SALEM, OHIO 44460 5.5 oz plastic bag UPC 8 55993 20018 6, heinen's Warrensville Heights, OH 44128 NET WT 10 oz tub UPC 0 36232 07703 9, Hickory Harvest FOODS Akron, OH 44319 5 oz plastic tube UPC 0 36232 07704 6, 7 oz plastic tube UPC 0 36232 07716 9, 10 oz plastic tub UPC 0 36232 07703 9 & 11 oz plastic tub UPC 0 36232 07702 2, IM Good 1.6 oz tube UPC 7 93724 80218 9, Liberty Candy & Nuts Inc .3 oz plastic tube UPC 6 08819 35672 3; Market Source 5 lb box, UPC 0 36232 07715 2; Raylicious 1.5 oz plastic tube UPC 8 55291 00192 8 & Sheetz Distribution Services, Claysburg, PA 19625 3.5 oz plastic bag UPC 7 59465 00784 9; SunOpta 50# bag; and Superior Brokerage 7oz. cup, UPC 8-10222-02129-1 and 9oz. rectangle container, UPC 8-10222-02022-5. INGREDIENTS: Sunflower Kernels, Sunflower Oil and/or Peanut Oil, with Citric Acid added as a Preservative, and Salt
Why the product was recalled
The firm was notified by their supplier that the products may be contaminated with Listeria monocytogenes.
Distribution information
Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MO, MS, MT, NC, ND, NE, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, VT, WA, WI & WY.
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: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.
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
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