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Stop using now Food recall · FDA · Published December 16, 2019

Munk Pack Bars Recalled for Undeclared Milk Allergen

Munk Pack recalls 35g Peanut Butter Dark Chocolate Nut & Seed Bars due to undeclared milk. Check your UPC and expiration date.

🇺🇸 FDA recall #F-0591-2020FoodMunk Pack ›
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Recalling firmMUNK PACK INC222 Railroad Ave · Greenwich, CT 06830-6308
✎ GovInfoNow plain-language explainer

Munk Pack Inc. is recalling individual 35-gram Peanut Butter Dark Chocolate Nut & Seed Bars because the product may contain undeclared milk. This is a significant concern for individuals with milk allergies or sensitivities, as consuming the bar could trigger an allergic reaction. The affected items were distributed in New York and Florida. Read more at govinfonow.com/recall/16149-munk-pack-bars-recalled-for-undeclared-milk-allergen.

Source Summary by GovInfoNow · govinfonow.com/recall/16149-munk-pack-bars-recalled-for-undeclared-milk-allergen · Updated October 11, 2026 · FDA enforcement record: FDA #F-0591-2020

Cite this page

“Munk Pack Bars Recalled for Undeclared Milk Allergen.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/16149-munk-pack-bars-recalled-for-undeclared-milk-allergen. Based on FDA recall #F-0591-2020 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0591-2020%22&limit=1).

The FDA announced on Dec. 16, 2019, that Munk Pack is recalling its Peanut Butter Dark Chocolate Nut & Seed Bars due to undeclared milk. Consumers should stop eating the product and contact the company for a refund.

How to tell if you have it

  • Brand: Munk Pack
  • Product: Peanut Butter Dark Chocolate Nut & Seed Bar, 35 g, individual unit
  • Lot codes: NOV052020, NOV062020
  • UPC: 853787005917
  • Sold in NY and FL

The hazard

The product may contain undeclared milk, which poses a risk to individuals with milk allergies. The FDA classified this as a Class II recall.

Context

GovInfoNow's records show MUNK PACK INC has one other recall on record since Feb. 21, 2018, involving mold growth in a protein cookie. Other recent recalls of similar products include Winfield's CWB Chocolate Bar Recall (April 27, 2026), The Better Bakehouse Donutful Donuts recall (Aug. 17, 2026), and Loard's Peanut Butter Fudge Ice Cream Recall (April 15, 2026).

How to tell if you have this one

Check if you have a Munk Pack Peanut Butter Dark Chocolate Nut & Seed Bar, 35 g, individual unit. Look for the expiration dates NOV052020 or NOV062020 and the UPC code 853787005917 on the packaging.

  • Brand
    Munk Pack
  • Product
    Munk Pack Peanut Butter Dark Chocolate Nut & Seed Bar, 35 g, individual unit
  • Category
    Food
FDA recall event · 4 products

All 4 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
    NY, FL
Recall numberProduct, codes & lotsQuantity
F-0590-2020Munk Pack Keto Nut and Seed Dark Chocolate Sea Salt Bar, 35 g, individual unit; NOV052020 and NOV062020 UPC: 853787005764N/A
F-0591-2020Munk Pack Peanut Butter Dark Chocolate Nut & Seed Bar, 35 g, individual unit; NOV052020 and NOV062020 UPC: 853787005917N/A
F-0592-2020Munk Pack Coconut Cocoa Chip Keto Granola Bar, 4 pack, 128 g; NOV042020 UPC: 853787005849N/A
F-0593-2020Munk Pack Almond Butter Cocoa Chip Keto Granola Bar, 4 pack, 128 g; NOV042020 UPC: 853787005481449 (total all four products, awaiting breakdown)
Based on the official FDA remedy

What to do — step by step

  1. Stop consuming the product

    Do not eat the recalled bars if you have them in your home, as they may contain undeclared milk.

  2. Check the packaging details

    Verify that your bar matches the 35 g size and has one of the specified expiration dates or UPC code.

  3. Contact the manufacturer for remedy information

    The recall record does not specify a return or refund process; contact Munk Pack Inc. directly for further instructions.

Where it went and when

Where it was distributed

Distributed in Florida and New York.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: yesNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest 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: yesFL

FDA distribution: “NY, FL” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Florida, New York.

Recall timeline

FDA terminated this recall 7 months after the firm started it.

1. Firm started the recall: Dec 16, 201912. Published in FDA’s Enforcement Report: Feb 12, 202023. FDA classified it Class II: Jun 8, 202034. FDA terminated the recall: Jul 29, 2020420192020
  1. Firm started the recall
  2. Published in FDA’s Enforcement Report
  3. FDA classified it Class II
  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-0591-2020 (December 16, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0591-2020 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