CLASS I Food recall · Reported 1 May 2019 · FDA Enforcement Report

Banana Puddin Base recalled by Denali Ingredients

Denali Ingredients is recalling Banana Puddin Base, distributed in Ohio, Pennsylvania. The recall was initiated on 16 Apr 2019 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot F016758, Exp 03/03/2019; Lot F017544, Exp 03/30/2019; Lot F021031, Exp 11/06/2019; Lot F021997 Exp 12/22/2019;
Quantity recalled6,096 lbs.

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-1304-2019
FDA event ID
82649
Recalling firm
Denali Ingredients, New Berlin, WI
Classification
Class I
Status
Terminated
Recall initiated
16 Apr 2019
FDA classified
23 Apr 2019
Reported
1 May 2019
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Undeclared Egg

Timeline

16 Apr 2019Recall initiated by company
23 Apr 2019Classified by FDA+7 days
1 May 2019Published in enforcement report+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Banana Puddin Base contains an undeclared egg sub-ingredient.

Product as listed by the FDA

Banana Puddin Base, item # 70 0559-1034, in 5 gallon plastic pail. Net Wt: 48 LBS. Ice Cream Flavoring. Store Refrigerated (35-45F) at all times. Denali Ingredients LLC, 2400 S. Calhoun Rd, New Berlin, WI 53151

Where it was distributed

OH, PA

OhioPennsylvania

Questions about this recall

Why was it recalled?

Banana Puddin Base contains an undeclared egg sub-ingredient.

Which lots are affected?

Lot F016758, Exp 03/03/2019; Lot F017544, Exp 03/30/2019; Lot F021031, Exp 11/06/2019; Lot F021997 Exp 12/22/2019;

Where was it sold?

OH, PA

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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