CLASS II Food recall · Reported 27 Jul 2016 · FDA Enforcement Report

Los Mart Chicharrin Lagrima (Palmex Rotini), Package recalled

Martinez Imports is recalling Los Mart Chicharrin Lagrima (Palmex Rotini), Package, distributed in New York. The recall was initiated on 27 Apr 2016 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesNo Codes
Quantity recalled14 cases total

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-1674-2016
FDA event ID
74404
Recalling firm
Martinez Imports, Passaic, NJ
Classification
Class II
Status
Terminated
Recall initiated
27 Apr 2016
FDA classified
18 Jul 2016
Reported
27 Jul 2016
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Undeclared Allergens
Product category
Other

Timeline

27 Apr 2016Recall initiated by company
18 Jul 2016Classified by FDA+82 days
27 Jul 2016Published in enforcement report+9 days

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

Reason for recall

NYSDAM sampled this product and sampling analysis revealed it contained undeclared Yellow #6.

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

Los Mart Chicharrin Lagrima (Palmex Rotini), 1 lb., Package & Distributed by Martinez Imports, 1 Market St., Bldg #6, Passaic, NJ 07055

Where it was distributed

NY

New York

Questions about this recall

Why was it recalled?

NYSDAM sampled this product and sampling analysis revealed it contained undeclared Yellow #6.

Which lots are affected?

No Codes

Where was it sold?

NY

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.

Other products in this recall event

4 other products · FDA event 74404

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