CLASS II Food recall · Reported 23 Nov 2016 · FDA Enforcement Report

Baptista Bakery & Pastry Inc. Italian Bread plastic recalled

Batista Bakery & Pastries is recalling Baptista Bakery & Pastry Inc. Italian Bread plastic, distributed in Massachusetts, Rhode Island. The recall was initiated on 23 Sep 2016 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesProduct manufctured prior to 9/23/16
Quantity recalled30 units

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-0472-2017
FDA event ID
75472
Recalling firm
Batista Bakery & Pastries, Bristol, RI
Classification
Class II
Status
Terminated
Recall initiated
23 Sep 2016
FDA classified
17 Nov 2016
Reported
23 Nov 2016
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Product category
Bread

Timeline

23 Sep 2016Recall initiated by company
17 Nov 2016Classified by FDA+55 days
23 Nov 2016Published in enforcement report+6 days

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

Reason for recall

Product labels fails to declare flour as wheat flour as required by FALCPA

Product as listed by the FDA

Baptista Bakery & Pastry Inc. Italian Bread, 16 oz. plastic

Where it was distributed

MA, RI

MassachusettsRhode Island

Questions about this recall

Why was it recalled?

Product labels fails to declare flour as wheat flour as required by FALCPA

Which lots are affected?

Product manufctured prior to 9/23/16

Where was it sold?

MA, RI

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.

Other products in this recall event

3 other products · FDA event 75472

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