CLASS I Food recall · Reported 11 Mar 2026 · FDA Enforcement Report

Karns Foods, Mini Dark Chocolate Raspberry Cups Clear recalled

Karns Prime And Fancy Foods is recalling Karns Foods, Mini Dark Chocolate Raspberry Cups Clear plastic tamper evident packs, 36-42, distributed in Pennsylvania. The recall was initiated on 30 Jan 2026 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codes07851, packed on 9/18/2025
Quantity recalled36-42 packs

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-0574-2026
FDA event ID
98377
Recalling firm
Karns Prime And Fancy Foods, Mechanicsburg, PA
Brand
Karns
Classification
Class I
Status
Terminated
Recall initiated
30 Jan 2026
FDA classified
17 Mar 2026
Reported
11 Mar 2026
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Undeclared Peanuts
Product category
Chocolate

Timeline

30 Jan 2026Recall initiated by company
11 Mar 2026Published in enforcement report+40 days
17 Mar 2026Classified by FDA+6 days

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

Reason for recall

Product may contain undeclared peanuts.

Product as listed by the FDA

Karns Foods, Mini Dark Chocolate Raspberry Cups, 8 oz Clear plastic tamper evident packs, 36-42 packed per breakout

Where it was distributed

The recalled product was only distributed in the State of Pennsylvania.

Pennsylvania

Questions about this recall

Why was it recalled?

Product may contain undeclared peanuts.

Which lots are affected?

07851, packed on 9/18/2025

Where was it sold?

The recalled product was only distributed in the State of Pennsylvania.

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.

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