CLASS II ONGOING Food recall · Reported 1 Apr 2026 · FDA Enforcement Report

Pan de Bono (Cheese Bread) per Paper Cardboard recalled

South Florida Food is recalling Pan de Bono (Cheese Bread) per Paper Cardboard, distributed in Florida. The recall was initiated on 9 Mar 2026 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot #: 02/26/26 Expiration date:07/26/2026
Quantity recalled15 master cardboard Box 100 units each, Net Wt 14.4 lb

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
H-0623-2026
FDA event ID
98547
Recalling firm
South Florida Food, Hollywood, FL
Brand
Pan
Classification
Class II
Status
Ongoing
Recall initiated
9 Mar 2026
FDA classified
24 Mar 2026
Reported
1 Apr 2026
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Undeclared Soy
Product category
Bread

Timeline

9 Mar 2026Recall initiated by company
24 Mar 2026Classified by FDA+15 days
1 Apr 2026Published 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

Undeclared Soy.

Product as listed by the FDA

Pan de Bono (Cheese Bread), 100 units per Paper Cardboard Box, Net Wt 14.4 lb. KEEP FROZEN

Where it was distributed

Products distribute in FL

Florida

Questions about this recall

Why was it recalled?

Undeclared Soy.

Which lots are affected?

Lot #: 02/26/26 Expiration date:07/26/2026

Where was it sold?

Products distribute in FL

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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