Helados La Tapatia Cappuccino Cups Recalled for Listeria Contamination
Helados La Tapatia is recalling Cappuccino 9 oz cups due to Listeria monocytogenes found in environmental sampling.
The agency’s classification
FDA (Food): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
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 3/5 (High).
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall involves a high-risk pathogen (Listeria monocytogenes) without reported illness, which aligns with the High severity criteria.
Plain-English summary
Helados La Tapatia, Inc. is recalling Cappuccino 9 oz cups because FDA environmental sampling detected Listeria monocytogenes. The contamination was found in 21 of 50 samples, with 11 of those positive samples located on food contact surfaces.
The affected products are identified by UPC 6 34242- 22009 6. These cups were distributed in California, Nevada, Arizona, Washington, Canada, and Guam.
Consumers should stop using the recalled products and follow instructions provided by the recalling firm or the FDA for disposal or return.
The recalled product
- Product
- Cappuccino 9 oz cups Helados La Tapatia Fresno, CA 93706
- Manufacturer
- Helados La Tapatia, Inc
- Category
- Food — Dairy / Frozen Desserts
- Hazard
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 units with UPC 6 34242- 22009 6.
Distribution
Part of a larger recall action
This product is one of 53 recalled by Helados La Tapatia, 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.
See all 53 products in this recall →Related recalls
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