# FDA recall F-2421-2016

> **Treehouse Foods** · Class I · food recall initiated 2016-05-03.

## Product

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: 1

## Reason for recall

TreeHouse Foods is recalling products that may be impacted by sunflower seeds  contaminated with Listeria monocytogenes.

## Distribution

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.

## Key facts

- **Recall number:** F-2421-2016
- **Recalling firm:** Treehouse Foods
- **Classification:** Class I
- **Product type:** food
- **Status:** Terminated
- **Initiation date:** 2016-05-03
- **Report date:** 2016-10-12
- **Termination date:** 2017-08-15

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Oak Brook, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=F-2421-2016

## Citation

> AI Analytics. FDA recall F-2421-2016. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/F-2421-2016. Source: US FDA. Licensed CC0.

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