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Use caution Food recall · FDA · Published March 8, 2017

Nestle Butterfinger Candy Bars Recall: Small Plastic Pieces Risk Cuts

Nestle recalls Butterfinger Peanut Butter Crisp Chocolate Candy Bars in 3-pack and 6-pack Snack Tray due to small rigid plastic pieces that may cause cuts during consumption. Check lot numbers for affected products.

🇺🇸 FDA recall #F-1734-2107FoodNestle ›
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Recalling firmNestle USA800 N Brand Blvd · Glendale, CA 91203-1245
✎ GovInfoNow plain-language explainer

What happened, in plain English

Nestle is recalling Butterfinger Peanut Butter Crisp Chocolate Candy Bars in 3-packs and 6-pack Snack Trays because they may contain small rigid plastic pieces that can cause cuts when eaten. This recall affects products with specific lot numbers and best-by dates. Read more at govinfonow.com/recall/22029-nestle-butterfinger-candy-bars-recall-small-plastic-pieces-risk-cuts.

Source Summary by GovInfoNow · govinfonow.com/recall/22029-nestle-butterfinger-candy-bars-recall-small-plastic-pieces-risk-cuts · Updated October 8, 2026 · FDA enforcement record: FDA #F-1734-2107

Cite this page

“Nestle Butterfinger Candy Bars Recall: Small Plastic Pieces Risk Cuts.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/22029-nestle-butterfinger-candy-bars-recall-small-plastic-pieces-risk-cuts. Based on FDA recall #F-1734-2107 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1734-2107%22&limit=1).

Why it’s dangerous

The candy bars may contain small rigid plastic pieces that can cause cuts or lacerations if swallowed or chewed. These pieces are small enough to be hidden in the candy bar but can be accidentally ingested during consumption.

Who’s affected

Anyone who owns or uses the recalled Butterfinger Peanut Butter Crisp Chocolate Candy Bars in 3-pack SharePack or 6-pack Snack Tray. Children and people with small hands are at higher risk of injury from the plastic pieces.

How to tell if you have this one

Check for the product names: 'Nestle Butterfinger Peanut Butter Crisp Chocolate Candy Bar in 3-pack SharePack (2.01 oz)' or 'in 6-pack Snack Tray (4.02oz)'. Look for lot numbers: 63425747W1-W3 for 3-packs or 63435747W1-W3 for 6-packs. The best by date is October 2017.

  • Brand
    Nestle
  • Product
    Nestle Butterfinger Peanut Butter Crisp Chocolate Candy Bar in 3-pack SharePack (2.01 oz); and in 6-pack Snack Tray
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Lot Numbers

    Look for lot numbers on the packaging: 63425747W1-W3 for 3-pack SharePacks or 63435747W1-W3 for 6-pack Snack Trays.

  2. Stop Using if Suspect

    If you have the recalled product, stop using it immediately to avoid potential cuts from small plastic pieces.

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Product was distributed to retail distribution companies throughout the United States.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA terminated this recall 3 months after the firm started it.

1. Firm started the recall: Mar 8, 201712. FDA classified it Class II: Apr 3, 201723. Published in FDA’s Enforcement Report: Apr 12, 201734. FDA terminated the recall: May 25, 201742017
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #F-1734-2107 (March 8, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1734-2107 to see it in context.
  • Plain-language summary written by qwen3:4b on October 8, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA