Bacalaitos Criollos, CODFISH FRYING MIX, 7 oz., packaged in a plastic bag, 24 packages (units) per cases of 7 onz.
Summary
The FDA issued a Class II for Bacalaitos Criollos, CODFISH FRYING MIX, 7 oz., packaged in a plastic bag, 24 pa by Avole, Inc.. Reason: Allergen not listed in the Contains statement: Fish.
Details
Source
Food Recall
External ID
F-1835-2024
Action Date
2024-10-02
Status
Terminated
Category
food
Product Description
Bacalaitos Criollos, CODFISH FRYING MIX, 7 oz., packaged in a plastic bag, 24 packages (units) per cases of 7 onz.
Lot/Code Info: 310925 EXP.06/2025
Quantity Affected: 100 Boxes of 24 units per box for a total of 2,400 units
Reason for Recall
Allergen not listed in the Contains statement: Fish
Distribution
Within Puerto Rico only. No foreign distribution.
Type: Voluntary: Firm initiated
Recall Initiated: 2024-09-09
Company
San Sebastian, PR
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 28 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Avole, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Avole, Inc. have FDA actions?
This is the only FDA action we have on record for Avole, Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1835-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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