CLASS II Food recall · Reported 16 Nov 2022 · FDA Enforcement Report

Gourmet Old-Fashioned Caramel Holiday Popcorn recalled

Rieckhoff Family Businesses is recalling Gourmet Old-Fashioned Caramel Holiday Popcorn, distributed in 8 states. The recall was initiated on 27 Oct 2022 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesAll lots and expiration dates
Quantity recalled20,870 boxes

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-0142-2023
FDA event ID
91082
Recalling firm
Rieckhoff Family Businesses, Sac City, IA
Classification
Class II
Status
Terminated
Recall initiated
27 Oct 2022
FDA classified
8 Nov 2022
Reported
16 Nov 2022
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Product category
Popcorn

Timeline

27 Oct 2022Recall initiated by company
8 Nov 2022Classified by FDA+12 days
16 Nov 2022Published 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

Label contains "Gluten Free" claim but product contains wheat and barley which are declared on the label.

Product as listed by the FDA

Gourmet Old-Fashioned Caramel Holiday Popcorn, 18oz box, UPC 25606 00061

Where it was distributed

Distribution Centers in AZ, GA, IN, KY, MD, NE, NY, and TX.

ArizonaGeorgiaIndianaKentuckyMarylandNebraskaNew YorkTexas

Questions about this recall

Why was it recalled?

Label contains "Gluten Free" claim but product contains wheat and barley which are declared on the label.

Which lots are affected?

All lots and expiration dates

Where was it sold?

Distribution Centers in AZ, GA, IN, KY, MD, NE, NY, and 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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