CLASS II Food recall · Reported 16 Nov 2016 · FDA Enforcement Report
Iberia Codfish Fritter Mix recalled by Productos La Finca
Productos La Finca is recalling Iberia Codfish Fritter Mix, distributed in Florida. The recall was initiated on 13 Jul 2016 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-0347-2017
- FDA event ID
- 74836
- Recalling firm
- Productos La Finca, Sabana Grande, PR
- Brand
- Iberia Codfish
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 13 Jul 2016
- FDA classified
- 8 Nov 2016
- Reported
- 16 Nov 2016
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Undeclared Allergens
- Product category
- Fish
Timeline
| 13 Jul 2016 | Recall initiated by company | |
| 8 Nov 2016 | Classified by FDA | +118 days |
| 16 Nov 2016 | Published 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 food allergen: Soy
Food allergen labelling is required by US law for the nine major allergens. A product recalled for an undeclared allergen is only a risk to people with that allergy; everyone else can consume it safely.
Product as listed by the FDA
Iberia Codfish Fritter Mix
Where it was distributed
USA only: Florida
Questions about this recall
Why was it recalled?
Undeclared food allergen: Soy
Which lots are affected?
Lot #16076, Exp. 3/16/17 and Lot # 16089, Exp. 3/29/17
Where was it sold?
USA only: Florida
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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