CLASS II Food recall · Reported 16 Oct 2019 · FDA Enforcement Report

Trail's End Chocolatey Carmel Crunch, in fundraiser tin recalled

weaver fundraising is recalling Trail's End Chocolatey Carmel Crunch, in fundraiser tin, distributed in Texas. The recall was initiated on 14 Sep 2019 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesFoil bag inside tin: ACP Caramel and 168304A9RK 201929 Case: 108304A9TE191929
Quantity recalled751 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-0020-2020
FDA event ID
83810
Recalling firm
weaver fundraising, Indianapolis, IN
Classification
Class II
Status
Terminated
Recall initiated
14 Sep 2019
FDA classified
7 Oct 2019
Reported
16 Oct 2019
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Undeclared Tree Nuts
Product category
Candy

Timeline

14 Sep 2019Recall initiated by company
7 Oct 2019Classified by FDA+23 days
16 Oct 2019Published 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

undeclared almonds, cashews, and pecans

Product as listed by the FDA

Trail's End Chocolatey Carmel Crunch, in 15oz fundraiser tin, distributed in six count wholesale cases marked as ACP Caramel Corn w/almonds.

Where it was distributed

Boy Scout troops in Houston and Corpus Christi TX

Texas

Questions about this recall

Why was it recalled?

undeclared almonds, cashews, and pecans

Which lots are affected?

Foil bag inside tin: ACP Caramel and 168304A9RK 201929 Case: 108304A9TE191929

Where was it sold?

Boy Scout troops in Houston and Corpus Christi 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.

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