CLASS II Food recall · Reported 31 Mar 2021 · FDA Enforcement Report

Buc-ee's Butter Toffee Almonds recalled by Lehi Valley Trading Co

Lehi Valley Trading is recalling Buc-ee's Butter Toffee Almonds, distributed in Texas. The recall was initiated on 12 Mar 2021 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot Code: 0091673, BEST By DATE: Sep 09, 2021
Quantity recalled96 cases (12 bags/case)

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-0352-2021
FDA event ID
87536
Recalling firm
Lehi Valley Trading, Mesa, AZ
Classification
Class II
Status
Terminated
Recall initiated
12 Mar 2021
FDA classified
23 Mar 2021
Reported
31 Mar 2021
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Labeling Errors
Product category
Candy

Timeline

12 Mar 2021Recall initiated by company
23 Mar 2021Classified by FDA+11 days
31 Mar 2021Published 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

Butter Toffee Peanuts mislabeled as Butter Toffee Almonds

Product as listed by the FDA

Buc-ee's Butter Toffee Almonds, 12 oz., packaged in clear zip top bag with stickered label, UPC: 0 9524842002 4, Manufactured and packaged at Lehi Valley Trading Company 4955 . McKellips Rd, Mesa, AZ 85215. branded and statement on label "Distributed by Buc-ee's LTD. 327 FM 2004 Lake Jackson, TX 77566. Store in clean, dry area at ambient temperature.

Where it was distributed

TX

Texas

Questions about this recall

Why was it recalled?

Butter Toffee Peanuts mislabeled as Butter Toffee Almonds

Which lots are affected?

Lot Code: 0091673, BEST By DATE: Sep 09, 2021

Where was it sold?

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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