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
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
- Brand
- Primera Negra
- 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 2017 | Recall initiated by company | |
| 27 Dec 2017 | Published in enforcement report | +121 days |
| 12 Jan 2018 | Classified 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.
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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