Blue Bunny Ice Cream Recall: Egg Not Listed on Label
Wells Enterprises recalls Blue Bunny Bordeaux Cherry Chocolate ice cream due to potential egg ingredient not listed on label. Consumers should check packaging for item #745152.
Lower-risk recall
The product may contain egg which is not listed on the ingredient label.
Contact the company
What happened, in plain English
Wells Enterprises is recalling Blue Bunny Bordeaux Cherry Chocolate ice cream because it may contain egg that isn't listed on the label. This could affect people with egg allergies who might experience allergic reactions. Read more at govinfonow.com/recall/30012-blue-bunny-ice-cream-recall-egg-not-listed-on-label.
Source Summary by GovInfoNow · govinfonow.com/recall/30012-blue-bunny-ice-cream-recall-egg-not-listed-on-label · Updated August 18, 2026 · FDA enforcement record: FDA #F-1961-2014
Cite this page
“Blue Bunny Ice Cream Recall: Egg Not Listed on Label.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/30012-blue-bunny-ice-cream-recall-egg-not-listed-on-label. Based on FDA recall #F-1961-2014 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1961-2014%22&limit=1).
Why it’s dangerous
The ice cream may contain egg that isn't listed on the label. This could cause allergic reactions in people who are sensitive or allergic to egg. The hazard is specific to those with egg allergies.
Who’s affected
People who have eaten or are likely to eat this ice cream product are at risk if they have egg allergies. Those with egg allergies should be cautious about consuming the product.
How to tell if you have this one
Check for the product name 'Blue Bunny Bordeaux Cherry Chocolate', 1.75 quart size, packaged in 4/56-oz carton cases. Look for item number 745152 on the packaging.
- Brand
Blue Bunny- Product
Blue Bunny Premium Ice Cream, Bordeaux Cherry Chocolate, 1.75 quart. Packaged in 4/56-oz carton cases. Item # 745152- Category
Food
What to do — step by step
Check Label
Look for the item number 745152 on the packaging to confirm if it's recalled.
Where it went and when
Where it was distributed
Distributed in 3 states.
FDA distribution: “The product was distributed to KS, IN and IA.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Indiana, Iowa, Kansas.
Recall timeline
FDA terminated this recall 3 months after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #F-1961-2014 (May 2, 2014) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1961-2014 to see it in context.
- Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.