CLASS II Food recall · Reported 8 Apr 2015 · FDA Enforcement Report

Trigger's Black Bean & Corn Salsa recalled by Creative Foodworks

Creative Foodworks is recalling Trigger's Black Bean & Corn Salsa, distributed in Arizona, Iowa, Louisiana, Tennessee, Texas. The recall was initiated on 2 Feb 2015 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot# 246JC4A and 283JC4A
Quantity recalled1980 units

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-1811-2015
FDA event ID
70429
Recalling firm
Creative Foodworks, San Antonio, TX
Classification
Class II
Status
Terminated
Recall initiated
2 Feb 2015
FDA classified
31 Mar 2015
Reported
8 Apr 2015
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Undeclared Peanuts
Product category
Dips & Spreads

Timeline

2 Feb 2015Recall initiated by company
31 Mar 2015Classified by FDA+57 days
8 Apr 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 may contain undeclared peanuts.

Product as listed by the FDA

Trigger's Black Bean & Corn Salsa NET Wt 16 Oz. - MEDIUM HEAT; Manufactured in San Antonio, TX for Trigger Beeler's Gourmet Foods

Where it was distributed

TX, LA, TN, AZ, IA

ArizonaIowaLouisianaTennesseeTexas

Questions about this recall

Is Trigger's Black Bean & Corn Salsa recalled?

Yes. Creative Foodworks recalled Trigger's Black Bean & Corn Salsa on 2 Feb 2015. The recall is Class II and its status is Terminated. Recall number F-1811-2015.

Why was it recalled?

Product may contain undeclared peanuts.

Which lots are affected?

Lot# 246JC4A and 283JC4A

Where was it sold?

TX, LA, TN, AZ, IA

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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