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

Meijer Honey Vanilla Bourbon Pecans Recall: Mislabeling Hazard

Meijer recalls 8.5 oz Honey Vanilla Bourbon Pecans due to mislabeling that omits key ingredients and falsely declares others, posing allergy risks.

🇺🇸 FDA recall #F-2375-2017FoodMeijer ›
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Recalling firmMeijer, Inc #816 - Grand River Packaging3040 Remico St SW · Grandville, MI 49418-1189
✎ GovInfoNow plain-language explainer

What happened, in plain English

Meijer is recalling its 8.5 oz. stand-up pouch of Honey Vanilla Bourbon Pecans because the label incorrectly lists ingredients. The packaging falsely claims the product contains cream, milk, and eggs, while failing to list actual ingredients like spices, salt, and bourbon whiskey. This mislabeling creates a risk for consumers with allergies or dietary restrictions who rely on accurate ingredient information. Read more at govinfonow.com/recall/21377-meijer-honey-vanilla-bourbon-pecans-recall-mislabeling-hazard.

Source Summary by GovInfoNow · govinfonow.com/recall/21377-meijer-honey-vanilla-bourbon-pecans-recall-mislabeling-hazard · Updated October 11, 2026 · FDA enforcement record: FDA #F-2375-2017

Cite this page

“Meijer Honey Vanilla Bourbon Pecans Recall: Mislabeling Hazard.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/21377-meijer-honey-vanilla-bourbon-pecans-recall-mislabeling-hazard. Based on FDA recall #F-2375-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2375-2017%22&limit=1).

Why it’s dangerous

The primary danger is allergic reaction for individuals sensitive to dairy or eggs, as the label incorrectly states these ingredients are present when they are not. Additionally, consumers relying on the label for other dietary needs may be misled by the omission of actual ingredients such as sulfites, celery seeds, and bourbon whiskey.

Who’s affected

Consumers in Illinois, Indiana, Kentucky, Michigan, Ohio, and Wisconsin who purchased the recalled pecans between November 1, 2017, and December 5, 2017. Individuals with allergies to milk, eggs, or cream are at specific risk due to the false declaration on the label.

How to tell if you have this one

Look for Meijer Honey Vanilla Bourbon Pecans in an 8.5 oz. stand-up pouch. Check the manufacturing date (11/1/2017-12/5/2017) and one of the following codes on the package: 09 6340, 09 6322Z, 09 6306, 09 6312, or 09 6322Y.

  • Brand
    Meijer
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Your Package

    Verify if your product matches the brand, size, and specific lot codes listed in the recall details.

  2. Review Ingredient List

    Note that the label incorrectly lists cream, milk, and eggs and omits several other ingredients like spices and bourbon whiskey.

Where it went and when

Where it was distributed

Distributed in 6 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: yesINOhio: yesOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: yesKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “Domestic: IL, IN, KY, MI, OH, WI, Foreign:None VA/DOD: None” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Illinois, Indiana, Kentucky, Michigan, Ohio, Wisconsin.

Recall timeline

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

1. Firm started the recall: May 8, 201712. FDA classified it Class II: Jun 16, 201723. Published in FDA’s Enforcement Report: Jun 28, 201734. FDA terminated the recall: Aug 7, 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-2375-2017 (May 8, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2375-2017 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 11, 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