CLASS IIFood recall · Reported 16 Jul 2014 · FDA Enforcement Report
Old 502 Sangria Ice Cream recalled by Koogee-Queen Anne
Koogee-Queen Anne is recalling Old 502 Sangria Ice Cream, distributed in Indiana, Kentucky. The recall was initiated on 10 Apr 2014 and the FDA has classified it as Class II.
Check your package
Lot, batch or date codesCodes on the products distributed to Comfy Cow retail locations are not tracked.
Quantity recalled3gal - 1 unit
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.
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
During an FDA inspection the firm was notified that their bulk product lacked labels. Due to the lack of ingredient statement, the firm failed to declare direct allergens for the products. The products also lacked the declaration that they are packaged in a facility that processes peanuts, tree nuts, wheat, milk and eggs.
Food allergen labelling is required by US law for the nine major allergens. A product recalled for an undeclared allergen is only a risk to people with that allergy; everyone else can consume it safely.
Product as listed by the FDA
Old 502 Sangria Ice Cream. Manufactured by: Koogee-Queen Anne, LLC, d/b/a The Comfy Cow 2221 Frankfort Ave, Louisville, KY 40206.
During an FDA inspection the firm was notified that their bulk product lacked labels. Due to the lack of ingredient statement, the firm failed to declare direct allergens for the products. The products also lacked the declaration that they are packaged in a facility that processes peanuts, tree nuts, wheat, milk and eggs.
Which lots are affected?
Codes on the products distributed to Comfy Cow retail locations are not tracked.
Where was it sold?
Distributed in the states of Indiana and Kentucky
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.