CLASS II Food recall · Reported 6 Mar 2019 · FDA Enforcement Report

Panque - Butter Pound Cake recalled by Gilda Industries

Gilda Industries is recalling Panque - Butter Pound Cake. The recall was initiated on 22 Jan 2019 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot # 9018 Exp. Date 3/19/2019, Lot # 9005 Exp. Date 3/5/2019 and Lot # 9012 Exp. Date 3/12/2019
Quantity recalled20 cases (16 units per case)

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-1137-2019
FDA event ID
82075
Recalling firm
Gilda Industries, Hialeah, FL
Brand
Panque
Classification
Class II
Status
Terminated
Recall initiated
22 Jan 2019
FDA classified
1 Mar 2019
Reported
6 Mar 2019
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Other Reasons
Product category
Cakes & Pastries

Timeline

22 Jan 2019Recall initiated by company
1 Mar 2019Classified by FDA+38 days
6 Mar 2019Published in enforcement report+5 days

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

Reason for recall

Failure to declare milk.

Product as listed by the FDA

Gilda Industries, Panque - Butter Pound Cake, Manufactured by and Distributed for Gilda Industries

Where it was distributed

Domestic consignees only.

Questions about this recall

Why was it recalled?

Failure to declare milk.

Which lots are affected?

Lot # 9018 Exp. Date 3/19/2019, Lot # 9005 Exp. Date 3/5/2019 and Lot # 9012 Exp. Date 3/12/2019

Where was it sold?

Domestic consignees only.

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 II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

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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