CLASS II Food recall · Reported 27 Aug 2014 · FDA Enforcement Report

Xochitl(so cheel) Chipotle Queso Dip recalled by Renfro Foods

Renfro Foods is recalling Xochitl(so cheel) Chipotle Queso Dip, distributed in Maine, Texas. The recall was initiated on 28 Feb 2014 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot Code FA2046252
Quantity recalled3552 jars (296 cases of 12/16 oz jars)

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-2340-2014
FDA event ID
67642
Recalling firm
Renfro Foods, Fort Worth, TX
Brand
Xochitl
Classification
Class II
Status
Terminated
Recall initiated
28 Feb 2014
FDA classified
20 Aug 2014
Reported
27 Aug 2014
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Product category
Dips & Spreads

Timeline

28 Feb 2014Recall initiated by company
20 Aug 2014Classified by FDA+173 days
27 Aug 2014Published in enforcement report+7 days

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

Reason for recall

Undeclared wheat due to a supplier's inadvertent use of a wheat product instead of whey in preparing the cheese pre-mix for the recalling firm.

Product as listed by the FDA

XOCHITL(so cheel) Chipotle Queso Dip; ALL NATURAL NO TRANS FAT; HOT; NET WT. 11.5 OZ (326g); DIST BY: XOCHITL (so cheel), INC. (214)800-351 DALLAS, TEXAS 75252

Where it was distributed

ME, TX

MaineTexas

Stores named: Chipotle

Questions about this recall

Why was it recalled?

Undeclared wheat due to a supplier's inadvertent use of a wheat product instead of whey in preparing the cheese pre-mix for the recalling firm.

Which lots are affected?

Lot Code FA2046252

Where was it sold?

ME, TX

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

2 other products · FDA event 67642

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