Houdini Inc. Recalls Alfasi Kosher Trio Basket Due to Salmonella Risk
Houdini Inc. is recalling Alfasi Kosher Trio Basket #812 due to potential Salmonella contamination. The product was distributed nationwide, including Puerto Rico.
The agency’s classification
FDA (Food): Class I
Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 5/5 (Critical).
Highest-severity recall. The hazard can cause serious injury or death. Stop using the product now and follow the agency's instructions.
Our severity reasoning: The agency classification is FDA Class I, which mandates a minimum severity score of 5 according to the rubric. Additionally, Salmonella is a high-risk pathogen.
Plain-English summary
Houdini Inc. is recalling 14 baskets of Alfasi Kosher Trio Basket #812 (Lot #LC446250) because of potential Salmonella contamination. The recall was initiated by the U.S. Food and Drug Administration.
The affected product was distributed nationwide, including Puerto Rico. The source text does not specify specific retail locations or dates of distribution.
Consumers who have purchased this product should stop using it immediately. The source text does not provide specific instructions for disposal or refund procedures, but consumers should generally follow guidance from the recalling firm or the FDA.
The recalled product
- Product
- Alfasi Kosher Trio Basket #812
- Manufacturer
- Houdini Inc.
- Category
- Food — Kosher Food
- Hazard
- Affected units
- 14
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)
- Lot #LC446250
Distribution
Part of a larger recall action
This product is one of 31 recalled by Houdini Inc. 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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