CLASS I Food recall · Reported 23 Jul 2025 · FDA Enforcement Report

Kilwin's Truffle Assortment recalled by Kilwin's Quality Confections

Kilwin's Quality Confections is recalling Kilwin's Truffle Assortment, distributed in 14 states. The recall was initiated on 27 May 2025 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesNone
Quantity recalled130lbs total across all recalled products

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
H-0282-2025
FDA event ID
97152
Recalling firm
Kilwin's Quality Confections, Petoskey, MI
Classification
Class I
Status
Terminated
Recall initiated
27 May 2025
FDA classified
17 Jul 2025
Reported
23 Jul 2025
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Undeclared Tree Nuts
Product category
Chocolate

Timeline

27 May 2025Recall initiated by company
17 Jul 2025Classified by FDA+51 days
23 Jul 2025Published in enforcement report+6 days

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

Reason for recall

undeclared pecans

Product as listed by the FDA

Kilwin's Truffle Assortment 9.5oz UPC 0 004574 0 Kilwin's Truffle Assortment 8oz UPC 0 043109 5 Kilwin's Truffle Assortment 4.75oz UPC 0 044121 8

Where it was distributed

NC, FL, MD, DE, MI, NH, IL, VA, OH, GA, AL, DC, TX, LA

AlabamaDistrict of ColumbiaDelawareFloridaGeorgiaIllinoisLouisianaMarylandMichiganNorth CarolinaNew HampshireOhioTexasVirginia

Questions about this recall

Why was it recalled?

undeclared pecans

Which lots are affected?

None

Where was it sold?

NC, FL, MD, DE, MI, NH, IL, VA, OH, GA, AL, DC, TX, LA

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 I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

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 97152

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