Lower risk Food recall · FDA · Published April 16, 2019

Denali Ingredients Banana Puddin Base Recall: Undeclared Egg Ingredient

Denali Ingredients LLC recalls Banana Puddin Base (item #70 0559-1034) due to undeclared egg sub-ingredient. Products sold in 5-gallon plastic pails with specific lot numbers and expiration dates.

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

🇺🇸 FDA recall #F-1304-2019Food Denali Ingredients ›

Lower-risk recall

Banana Puddin Base contains an undeclared egg sub-ingredient.

Take action

Contact the company

Recalling firmDenali Ingredients LLC2400 S Calhoun Rd · New Berlin, WI 53151-2710

✎ GovInfoNow plain-language explainer

Denali Ingredients LLC is recalling Banana Puddin Base (item #70 0559-1034) because it contains an undeclared egg sub-ingredient. This could pose a risk for people with egg allergies. The product is sold in 5-gallon plastic pails and must be discarded if you have it. Read more at govinfonow.com/recall/17561-denali-ingredients-banana-puddin-base-recall-undeclared-egg-ingredient.

Source Summary by GovInfoNow · govinfonow.com/recall/17561-denali-ingredients-banana-puddin-base-recall-undeclared-egg-ingredient · Updated October 5, 2026 · FDA enforcement record: FDA #F-1304-2019

Cite this page

“Denali Ingredients Banana Puddin Base Recall: Undeclared Egg Ingredient.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/17561-denali-ingredients-banana-puddin-base-recall-undeclared-egg-ingredient. Based on FDA recall #F-1304-2019 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1304-2019%22&limit=1).

The FDA announced on April 16, 2019, that Denali Ingredients LLC is recalling Banana Puddin Base due to an undeclared egg sub-ingredient. The recall affects products distributed in Ohio and Pennsylvania.

How to tell if you have it

Denali Ingredients Banana Puddin Base
Item # 70 0559-1034
5 gallon plastic pail
Net Wt: 48 LBS
Lot F016758, Exp 03/03/2019
Lot F017544, Exp 03/30/2019
Lot F021031, Exp 11/06/2019
Lot F021997 Exp 12/22/2019

The hazard

The Banana Puddin Base contains an undeclared egg sub-ingredient, according to the FDA. The product is classified as a Class I recall.

Context

GovInfoNow's records show Denali Ingredients LLC has 1 other recall on record since 2020-10-19. Other recent recalls of similar products include Lunds & Byerlys Monster Cookies Recall (2025-12-03), Blank Slate Creamery Vegan Coconut Fudge Sandwiches Recall (2026-08-01), and 529 Commerce Aquafaba Powder Recall (2026-07-28).

How to tell if you have this one

Check for the product name 'Banana Puddin Base', item number #70 0559-1034, in 5-gallon plastic pails. Look for lot numbers F016758 (exp 03/03/2019), F017544 (exp 03/30/2019), F021031 (exp 11/06/2019), or F021997 (exp 12/22/2019).

Brand
Denali Ingredients
Category
Food

Based on the official FDA remedy

What to do — step by step

Check Product Details
Identify the product by checking for the item number #70 0559-1034 and the specific lot numbers listed in the recall notice.
Discard Product
If you have the recalled Banana Puddin Base, discard it immediately to avoid potential allergic reactions.

Where it went and when

Where it was distributed

Distributed in Ohio and Pennsylvania.

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

States: Ohio, Pennsylvania.

Recall timeline

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

Apr 16, 2019Firm started the recall
Apr 23, 2019FDA classified it Class I
May 1, 2019Published in FDA’s Enforcement Report
Jun 27, 2019FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

Similar recalls

Latest food recalls

Keep exploring

Link to this recall

<a href="https://govinfonow.com/recall/17561-denali-ingredients-banana-puddin-base-recall-undeclared-egg-ingredient">Denali Ingredients Banana Puddin Base Recall: Undeclared Egg Ingredient (GovInfoNow)</a>

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-1304-2019 (April 16, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1304-2019 to see it in context.
Plain-language summary written by qwen3:4b on October 5, 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.