CLASS II Food recall · Reported 27 Dec 2017 · FDA Enforcement Report

Primera Negra, Artificial Vanilla Flavoring recalled

Gonzalez Wholesale Distributor,l is recalling Primera Negra, Artificial Vanilla Flavoring, distributed in Florida. The recall was initiated on 28 Aug 2017 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot 07 2016; Exp Date: Dec 2017
Quantity recalled25 cases/24 units ea.

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-0570-2018
FDA event ID
78121
Recalling firm
Gonzalez Wholesale Distributor,l, Sanford, FL
Classification
Class II
Status
Terminated
Recall initiated
28 Aug 2017
FDA classified
12 Jan 2018
Reported
27 Dec 2017
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Other Reasons
Product category
Other

Timeline

28 Aug 2017Recall initiated by company
27 Dec 2017Published in enforcement report+121 days
12 Jan 2018Classified by FDA+16 days

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

Reason for recall

Product contains Coumarin.

Product as listed by the FDA

Primera Negra, Artificial Vanilla Flavoring NET WT 4 OZ and 8 OZ

Where it was distributed

Florida consignees only.

Florida

Questions about this recall

Is Primera Negra, Artificial Vanilla Flavoring recalled?

Yes. Gonzalez Wholesale Distributor,l recalled Primera Negra, Artificial Vanilla Flavoring on 28 Aug 2017. The recall is Class II and its status is Terminated. Recall number F-0570-2018.

Why was it recalled?

Product contains Coumarin.

Which lots are affected?

Lot 07 2016; Exp Date: Dec 2017

Where was it sold?

Florida 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 21 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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