CLASS III Food recall · Reported 22 Jul 2015 · FDA Enforcement Report

Del Campo Alino Casero Seasoning Paste recalled by Megabusiness

Megabusiness is recalling Del Campo Alino Casero Seasoning Paste, distributed in New Jersey, New York. The recall was initiated on 18 Dec 2014 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesAll lots
Quantity recalled192 bottles

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-2843-2015
FDA event ID
71472
Recalling firm
Megabusiness, Danbury, CT
Classification
Class III
Status
Terminated
Recall initiated
18 Dec 2014
FDA classified
14 Jul 2015
Reported
22 Jul 2015
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Undeclared Allergens
Product category
Fish

Timeline

18 Dec 2014Recall initiated by company
14 Jul 2015Classified by FDA+208 days
22 Jul 2015Published 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

Product contains undeclared preservatives, Benzoic Acid and Sorbic Acid.

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

Del Campo Alino Casero Seasoning Paste, 15oz; Product Code: 03138; UPC: 7 751227 000894. Product is in a glass bottle.

Where it was distributed

NY and NJ

New JerseyNew York

Questions about this recall

Why was it recalled?

Product contains undeclared preservatives, Benzoic Acid and Sorbic Acid.

Which lots are affected?

All lots

Where was it sold?

NY and NJ

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 III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

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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