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Lower risk Food recall · FDA · Published January 10, 2022

Brownie Points Schmurtle 2oz Pack: Missing Peanuts Allergen Label

Brownie Points recalls Schmurtle 2oz gift filler packs for missing peanut allergen label. Consumers should check lot number 754 for affected items.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #F-0615-2022FoodBrownie Points ›
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Contact the company

Recalling firmBrownie Points LLC5712 Westbourne Ave · Columbus, OH 43213-1400
✎ GovInfoNow plain-language explainer

Brownie Points is recalling its Schmurtle 2oz gift filler packs because they don't list peanuts as an allergen on the label. This could cause allergic reactions for people sensitive to peanuts. Read more at govinfonow.com/recall/13394-brownie-points-schmurtle-2oz-pack-missing-peanuts-allergen-label.

Source Summary by GovInfoNow · govinfonow.com/recall/13394-brownie-points-schmurtle-2oz-pack-missing-peanuts-allergen-label · Updated October 4, 2026 · FDA enforcement record: FDA #F-0615-2022

Cite this page

“Brownie Points Schmurtle 2oz Pack: Missing Peanuts Allergen Label.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/13394-brownie-points-schmurtle-2oz-pack-missing-peanuts-allergen-label. Based on FDA recall #F-0615-2022 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0615-2022%22&limit=1).

Brownie Points LLC voluntarily recalled its Brownie Points Schmurtle 2oz packaged product on Jan. 10, 2022, according to the FDA. The recall was issued because the label does not include peanuts, an undeclared allergen. Owners should contact the company for a refund.

How to tell if you have it

  • Brand: Brownie Points
  • Product: Schmurtle 2oz Packaged in food grade cellophane
  • Lot Number: 754
  • Quantity: 209 units

The hazard

The product contains peanuts that are not declared on the label, posing a risk to individuals with peanut allergies. The FDA classified this as a Class II recall.

Context

GovInfoNow's records show other recent recalls of similar products include Tiki Bar Candy Dark Chocolatey Peanut Butter & Pretzel (2026-01-30) and Albertsons Pop Dots Coco & Hazelnut 6ct (2026-05-06). Einstein Bros Bagels Honey Almond Spread was also recalled on 2026-03-26 for an undeclared almond allergen.

How to tell if you have this one

Check for the lot number 754 on the food-grade cellophane packaging. These packs are only sold as gift basket fillers and not individually.

  • Brand
    Brownie Points
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for the lot number 754 on the food-grade cellophane packaging to confirm if it's affected.

Where it went and when

Where it was distributed

Distributed in 46 states.

Alaska: not listedAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: not listedRIMassachusetts: 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: not listedNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: not listedDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: not listedHITexas: yesTXFlorida: yesFL

FDA distribution: “AL, AR, AZ, CA, CO, CT, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Alabama, Arizona, Arkansas, California, Colorado, Connecticut, Delaware, Florida, Georgia, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nebraska, Nevada, New Hampshire, New Jersey, New York, North Carolina, North Dakota, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, South Dakota, Tennessee, Texas, Utah, Vermont, Virginia, Washington, West Virginia, Wisconsin, Wyoming.

Recall timeline

FDA terminated this recall 43 days after the firm started it.

1. Firm started the recall: Jan 10, 202212. FDA classified it Class II: Jan 25, 202223. Published in FDA’s Enforcement Report: Feb 2, 202234. FDA terminated the recall: Feb 22, 202242022
  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-0615-2022 (January 10, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0615-2022 to see it in context.
  • Plain-language summary written by qwen3:4b on October 4, 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