Blue Bell Magic Cookie Bar Recalled Due to Listeria Infections
Blue Bell Creameries is recalling Magic Cookie Bar One Pint containers because 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 agency classification is FDA Class I, and the source text explicitly reports that five patients were infected with Listeria monocytogenes, meeting the criteria for a Critical severity score.
Plain-English summary
Blue Bell Creameries, L.P. is recalling Blue Bell Magic Cookie Bar One Pint (473 mL) containers. The recall involves 684,725 units with all lot codes within expiry. The product was distributed across 24 U.S. states and numerous international locations, including Bermuda, Belize, and various countries in the Middle East, Asia, and the Caribbean.
The recall was initiated after five patients treated in a single hospital in Kansas were infected with one of four rare strains of Listeria monocytogenes. This bacterial infection is the specific reason for the market withdrawal of the affected ice cream bars.
Consumers who have purchased this product should check their freezers for the specific item described. If found, they should discard the product or return it to the place of purchase for a refund. The source text does not provide specific instructions on how to dispose of the product or contact information for the manufacturer.
The recalled product
- Product
- Blue Bell Magic Cookie Bar One Pint (473 mL)
- Manufacturer
- Blue Bell Creameries, L.P.
- Category
- Food — Frozen Desserts
- Hazard
- Affected units
- 684,725
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.
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