CLASS II Food recall · Reported 11 Mar 2015 · FDA Enforcement Report

Herdez Chilpotle Peppers recalled by MegaMex Foods, LLC - R&D

MegaMex Foods LLC - R&D Center is recalling Herdez Chilpotle Peppers, distributed nationwide in the US. The recall was initiated on 6 Feb 2015 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot Numbers: LF 01304, LF 01314, LF 02014, LF 05084, LF 05094, LF 05294, LF 05304, LF 05314, LF 06174, LF 06244, LF 06254, LF 06264, LF 10184, LF 10214, LF 10224, LF 10234.
Quantity recalled58,749 cases

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-1379-2015
FDA event ID
70476
Recalling firm
MegaMex Foods LLC - R&D Center, Orange, CA
Classification
Class II
Status
Terminated
Recall initiated
6 Feb 2015
FDA classified
3 Mar 2015
Reported
11 Mar 2015
Type
Voluntary: Firm initiated
Customers notified by
Letter
Product category
Peppers

Timeline

6 Feb 2015Recall initiated by company
3 Mar 2015Classified by FDA+25 days
11 Mar 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

MegaMex Foods is recalling Herdez Chilpotle Peppers product due to an undeclared wheat allergen.

Product as listed by the FDA

Herdez Chilpotle Peppers, 7oz., Item No. 52738, UPC 072878285131

Where it was distributed

Nationwide in US

Nationwide

Questions about this recall

Why was it recalled?

MegaMex Foods is recalling Herdez Chilpotle Peppers product due to an undeclared wheat allergen.

Which lots are affected?

Lot Numbers: LF 01304, LF 01314, LF 02014, LF 05084, LF 05094, LF 05294, LF 05304, LF 05314, LF 06174, LF 06244, LF 06254, LF 06264, LF 10184, LF 10214, LF 10224, LF 10234.

Where was it sold?

Nationwide in US

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 Peppers recalls

All 179