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Lower risk Food recall · FDA · Published June 14, 2017

GoMacro MACROBAR Recall: Listeria Contamination Risk

GoMacro is recalling MACROBAR snacks due to potential Listeria monocytogenes contamination. Affected products include specific sizes and UPC codes with dates up to February 2018.

🇺🇸 FDA recall #F-2413-2017FoodGoMacro ›
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Recalling firmGoMacro, Inc.415 S Wagoner Ave · Viola, WI 54664-8511
✎ GovInfoNow plain-language explainer

What happened, in plain English

GoMacro is recalling certain MACROBAR snacks that may contain Listeria monocytogenes, a bacteria that can cause foodborne illness. Consumers should check the product details and take action if they have the affected items. Read more at govinfonow.com/recall/20759-gomacro-macrobar-recall-listeria-contamination-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/20759-gomacro-macrobar-recall-listeria-contamination-risk · Updated October 8, 2026 · FDA enforcement record: FDA #F-2413-2017

Cite this page

“GoMacro MACROBAR Recall: Listeria Contamination Risk.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/20759-gomacro-macrobar-recall-listeria-contamination-risk. Based on FDA recall #F-2413-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2413-2017%22&limit=1).

Why it’s dangerous

Listeria monocytogenes is a bacteria that can cause serious foodborne illness, especially in pregnant women, newborns, and people with weakened immune systems. Contaminated products may lead to infection if eaten.

Who’s affected

Anyone who purchased GoMacro MACROBAR snacks with the listed UPC codes and dates. People with weakened immune systems are at higher risk for foodborne illness.

How to tell if you have this one

Check for the product name 'go macro MACROBAR, coconut + almond butter + chocolate chips' with specific sizes: 0.9 oz (25g) or 2.3 oz (65g). Look for UPC codes 8 53555-00671 9 or 8 53555-00668 9 and lot codes from 3516 to 3571 with best by dates up to February 2018.

  • Brand
    GoMacro
  • Product
    go macro MACROBAR, coconut + almond butter + chocolate chips, in the following sizes: 1. Net Wt 0.9 oz / 25 G minbar
  • Category
    Food
FDA recall event · 3 products

All 3 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    Terminated
  • Distribution
    Nationwide and Canada
Recall numberProduct, codes & lotsQuantity
F-2413-2017go macro MACROBAR, coconut + almond butter + chocolate chips, in the following sizes: 1. Net Wt 0.9 oz / 25 G minbar, UPC 8 53555-00671 9 and 2. net Wt 2.3 oz / 65 G, UPC 8 53555-00668 9; Lot Code / Best By Date: 3516 / 1/3/2018, 3525 / 1/10/2 018, 3536 / 1/16/2018, 3553 / 1/26/2018, 3571 / 2/6/2018. Mini's Lot Code / Best By Date: 3537 / 1/16/2018, 3570 / 2/6/2018.311,706 bars
F-2414-2017go macro THRIVE Chocolate, Nuts & Sea Salt bar, Net Wt 1.4 oz / 40 G, UPC 8 53555-00650 4; Lot Code / Best By Date: 3569 / 2/6/2018, 3576 / 2/9/20182651 bars
F-2415-2017go macro THRIVE Caramel Coconut bar, Net Wt 1.4 oz / 40 G, UPC 8 53555-00652 8; Lot Code / Best By Date: 3568 / 2/6/2018.1875 bars
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Verify the product size, UPC code, and lot code against the list provided in the recall notice.

Where it went and when

Where it was distributed

Distributed nationwide, and outside the U.S.

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: “Nationwide and Canada” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide, and outside the U.S.

Recall timeline

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

1. Firm started the recall: Jun 14, 201712. FDA classified it Class II: Jun 30, 201723. Published in FDA’s Enforcement Report: Jul 12, 201734. FDA terminated the recall: Sep 14, 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-2413-2017 (June 14, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2413-2017 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