The Recall Desk
CriticalFDA (Food)·F-2610-2015·Announced 2015-07-01

Blue Bell Ice Cream Cake Batter Recalled Due to Listeria Infections

Blue Bell Creameries is recalling Ice Cream Cake Batter 3 Gallon units after five patients in Kansas were infected with Listeria monocytogenes.

What this means for you

Highest-severity recall. Risk of serious injury or death is documented or strongly suspected. Stop using the product now and follow the agency's instructions.

Our severity reasoning: The source text explicitly states that five patients were infected with Listeria monocytogenes, and the agency classification is FDA Class I. Per the rubric, FDA Class I recalls and reported illnesses/infections warrant a Critical (5) severity score.

Plain-English summary

Blue Bell Creameries, L.P. is recalling 10,430 units of Blue Bell Ice Cream Cake Batter 3 Gallon. The recall covers all lot codes within the expiry date. The product was distributed across numerous U.S. states, including Florida, Georgia, and Texas, as well as various international locations such as Bermuda, Mexico, and China.

The recall was initiated because five patients treated in a single hospital in Kansas were infected with one of four rare strains of Listeria monocytogenes. This pathogen is associated with the recalled product.

Consumers who have purchased this product should check their inventory for the specific product name and quantity. If the product is found, it should be discarded or returned to the place of purchase. No specific instructions for disposal are provided in the source text beyond the standard recall protocol.

The recalled product

Product
Blue Bell Ice Cream Cake Batter 3 Gallon
Affected units
10,430

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • all lot codes within expiry

Distribution

Part of a larger recall action

This product is one of 286 recalled by Blue Bell Creameries, L.P. under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 286 products in this recall →