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Use caution Food recall · FDA · Published December 5, 2017

HERB-OX Beef Bouillon Recall: Undeclared Milk Allergen Risk

Creative Contract Packaging recalls HERB-OX Beef Flavor Granulated Bouillon jars from Sept 2020 and Oct 2020 due to potential undeclared milk allergen. Consumers should check jar codes and contact for details.

🇺🇸 FDA recall #F-0554-2018FoodCreative Contract Packaging ›
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Contact the company

Recalling firmCreative Contract Packaging Corporation, LLC3777 and 3837 Exchange Ave · Aurora, IL 60504-8102
✎ GovInfoNow plain-language explainer

What happened, in plain English

Creative Contract Packaging is recalling HERB-OX Beef Flavor Granulated Bouillon jars with 'Best If Used By' dates of September 2020 and October 2020 because they may contain an undeclared milk allergen. This poses a risk for people with milk allergies who could experience an allergic reaction. Read more at govinfonow.com/recall/19981-herb-ox-beef-bouillon-recall-undeclared-milk-allergen-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/19981-herb-ox-beef-bouillon-recall-undeclared-milk-allergen-risk · Updated October 7, 2026 · FDA enforcement record: FDA #F-0554-2018

Cite this page

“HERB-OX Beef Bouillon Recall: Undeclared Milk Allergen Risk.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/19981-herb-ox-beef-bouillon-recall-undeclared-milk-allergen-risk. Based on FDA recall #F-0554-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0554-2018%22&limit=1).

Why it’s dangerous

The product may contain milk as an allergen that was not declared on the label. This can cause allergic reactions in people who are sensitive to milk, including potentially serious reactions like hives, swelling, or difficulty breathing.

Who’s affected

People who have purchased HERB-OX Beef Flavor Granulated Bouillon jars with 'Best If Used By' dates of September 2020 or October 2020 are affected. Those with milk allergies are at higher risk of an allergic reaction.

How to tell if you have this one

Check the jar for a 'Best If Used By' date of September 2020 or October 2020. The code date is printed on top of the lid.

  • Brand
    Creative Contract Packaging
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Date

    Look for a 'Best If Used By' date of September 2020 or October 2020 on the jar lid.

Where it went and when

Where it was distributed

Distributed in 21 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: yesMNIllinois: not listedILWisconsin: yesWIMichigan: not listedMINew York: yesNYRhode Island: not listedRIMassachusetts: yesMAOregon: yesORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: yesIAIndiana: yesINOhio: not listedOHPennsylvania: yesPANew Jersey: not listedNJConnecticut: yesCTCalifornia: yesCAUtah: not listedUTColorado: yesCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: yesVAMaryland: not listedMDDelaware: yesDEArizona: yesAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: yesNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: yesGAHawaii: not listedHITexas: yesTXFlorida: yesFL

FDA distribution: “Domestic: AZ, CA, CO, CT, DE, IA,ID, IN, MN, NC, GA, OR, PA, NY, WI, WA, MA, TX, FL, GA, VA, NH Foreign:None VA/DOD:None” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Arizona, California, Colorado, Connecticut, Delaware, Florida, Georgia, Idaho, Indiana, Iowa, Massachusetts, Minnesota, New Hampshire, New York, North Carolina, Oregon, Pennsylvania, Texas, Virginia, Washington, Wisconsin.

Recall timeline

FDA terminated this recall 2 months after the firm started it.

1. Firm started the recall: Dec 5, 201712. Published in FDA’s Enforcement Report: Dec 27, 201723. FDA classified it Class I: Jan 8, 201834. FDA terminated the recall: Feb 12, 2018420172018
  1. Firm started the recall
  2. Published in FDA’s Enforcement Report
  3. FDA classified it Class I
  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-0554-2018 (December 5, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0554-2018 to see it in context.
  • Plain-language summary written by qwen3:4b on October 7, 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