Recall record at a glance
| Official record | F-2421-2016 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Treehouse Foods |
| Report date | Oct 12, 2016 |
| Recall initiation date | May 3, 2016 |
| Quantity | 92,865 cases for all products |
| Location | Oak Brook, IL, United States |
Official product description
UPC 1373312015, Meijer Peanut Butter Dark Chocolate Protein Bars,Best By/Date Code: DEC 05 16, JAN 04 17. UPC 3225108607, Family Gourmet Peanut Butter Dark Chocolate Protein ,Bars Best By/Date Code: JAN 04 17. UPC 3680039453, Food Club Peanut Butter Dark Chocolate Protein Bars,Best By/Date Code: DEC 05 16, JAN 04 17. UPC 4130304540, Essential Everyday Peanut Butter Dark Chocolate Protein Bars, Best By/Date Code: DEC 05 16, JAN 04 17. UPC 5042847944 , Gold Emblem Peanut Butter Dark Chocolate Protein Bars ,Best By/Date Code: DEC 05 16, JAN 04 17, JAN 05 17. UPC 7003863811, Best Choice Peanut Butter Dark Chocolate Protein Bars,Best By/Date Code: DEC 05 16, JAN 04 17. UPC 7025322720, Our Family Peanut Butter Dark Chocolate Protein Bars,Best By/Date Code: DEC 05 16, JAN 04 17. UPC 7078447478, Tops Peanut Butter Dark Chocolate Protein Bars, Best By/Date Code: JAN 04 17. UPC 7874203428, Great Value Peanut Butter Dark Chocolate Protein Bars, Best By/Date Code: 12 05 16, 12 06 16, 01 05 17, 01 06 17. UPC 7989380098, Eating Right (Lucerne) Peanut Butter Dark Chocolate Protein Bars, Best By/Date Code: DEC 05 16, JAN 05 17.
Why the product was recalled
TreeHouse Foods is recalling products that may be impacted by sunflower seeds contaminated with Listeria monocytogenes.
Distribution information
US: AL, AZ, AR, CA, CO, CT, FL, IL, IN, IA, KS,KY, LA, ME, MD, MA, MI, MN, MS, MO, NE, NV, NM, NY, NC,ND, OH, OK, OR, PA,SC, TN, TX, UT, VA, WA, WI, WY. OUS: HONDURAS, NICARAGUA, CHILE.
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: Telephone.
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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