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Lower risk Food recall · FDA · Published October 19, 2020

Denali Ingredients Coffee Cream Stabilizer Recall: Citric Acid Instead of Sodium Citrate

Denali Ingredients LLC recalls 50-lb coffee cream stabilizer bags due to incorrect citric acid use. This may affect food safety. Contact for remedy details.

🇺🇸 FDA recall #F-0122-2021FoodDenali Ingredients ›
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Recalling firmDenali Ingredients LLC2400 S Calhoun Rd · New Berlin, WI 53151-2710
✎ GovInfoNow plain-language explainer

Denali Ingredients LLC is recalling coffee cream stabilizer products because they were made with citric acid instead of sodium citrate. This could lead to food safety issues if used in coffee cream products. Read more at govinfonow.com/recall/15065-denali-ingredients-coffee-cream-stabilizer-recall-citric-acid-instead-of.

Source Summary by GovInfoNow · govinfonow.com/recall/15065-denali-ingredients-coffee-cream-stabilizer-recall-citric-acid-instead-of · Updated October 4, 2026 · FDA enforcement record: FDA #F-0122-2021

Cite this page

“Denali Ingredients Coffee Cream Stabilizer Recall: Citric Acid Instead of Sodium Citrate.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/15065-denali-ingredients-coffee-cream-stabilizer-recall-citric-acid-instead-of. Based on FDA recall #F-0122-2021 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0122-2021%22&limit=1).

The FDA announced on Oct. 19, 2020, that Denali Ingredients LLC is recalling Denali Ingredients Supreme1251 Coffee Cream Stabilizer because it was made with Citric Acid instead of Sodium Citrate. The agency said the error could pose an allergy risk to consumers sensitive to citrus or citrates.

How to tell if you have it

  • Brand: Denali Ingredients
  • Product: Supreme1251 Coffee Cream Stabilizer
  • Item Number: 501251-1014
  • Size: 50 lb. bag
  • Lot Code: F031582, Best If Used By: 08/18/22
  • Lot Code: F031263, Best If Used By: 08/14/22
  • Distribution: FL and OH

The hazard

The stabilizer was manufactured with Citric Acid instead of the intended Sodium Citrate. The FDA said this substitution could present an allergy risk to individuals sensitive to these ingredients.

Context

GovInfoNow's records show Denali Ingredients LLC has one other recall on record since April 16, 2019, specifically for Banana Puddin Base due to undeclared egg ingredient. Other recent recalls of similar products include Coffee Connexion Cheese Sauce Mix (May 6, 2026), Cold Prep Cream Sauce (May 6, 2026), and Alfredo Sauce (May 6, 2026).

How to tell if you have this one

Check for the product name 'Denali Ingredients Supreme1251 Coffee Cream Stabilizer', item number 501251-1014, and 50 lb. bags. The lot codes F031582 (best by 08/18/22) and F031263 (best by 08/14/22) are also indicators.

  • Brand
    Denali Ingredients
  • Category
    Food
FDA recall event · 2 products

All 2 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 III
  • Status
    Terminated
  • Distribution
    FL and OH
Recall numberProduct, codes & lotsQuantity
F-0121-2021Denali Ingredients Cream Tech 250 Sour Cream Stabilizer, Item 500120-1014, 50 lb. bag. Storage: For maximum Freshness Store at Ambient Temperatures Below 85F. This container is intended for Food Products Only. No other Use Authorized. Dispose of in an Approved Manner.; Lot Code: F031561 Best If Used By: 08/27/21 Mfg Date: 08/27/202250 lbs.
F-0122-2021Denali Ingredients Supreme1251Coffee Cream Stabilizer, Item 501251-1014, 50 lb. bag. Storage: For maximum Performance Store at Ambient Temperatures Below 85F. This container is intended for Food Products Only. No other Use Authorized. Dispose of in an Approved Manner.; Lot Code: F031582, Best If Used By: 08/18/22 Lot Code: F031263, Best If Used By: 08/14/223050 lbs.
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for the product name, item number, and lot codes on the packaging to confirm if it's recalled.

Where it went and when

Where it was distributed

Distributed in Florida and Ohio.

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: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: yesOHPennsylvania: 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: “FL and OH” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Florida, Ohio.

Recall timeline

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

1. Firm started the recall: Oct 19, 202012. FDA classified it Class III: Nov 19, 202023. Published in FDA’s Enforcement Report: Nov 25, 202034. FDA terminated the recall: Dec 30, 202042020
  1. Firm started the recall
  2. FDA classified it Class III
  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-0122-2021 (October 19, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0122-2021 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