Ham & Cotija Torta Sandwich on Telera Roll, 8.3 oz, plastic container, UPC 100001002017
Summary
The FDA issued a Class I for Ham & Cotija Torta Sandwich on Telera Roll, 8.3 oz, plastic container, UPC 10000 by COMPASS GROUP USA, INC.. Reason: Listeria monocytogenes. The recalled Cotija cheese was repackaged into finished RTE Sprig and Sprout Ham and Cotija Torta Sandwich on Telera Roll..
Details
Source
Food Recall
External ID
F-0910-2024
Action Date
2024-02-28
Status
Terminated
Category
food
Product Description
Ham & Cotija Torta Sandwich on Telera Roll, 8.3 oz, plastic container, UPC 100001002017
Lot/Code Info: USE BY DATES 02/09/24 to 02/16/24
Quantity Affected: 206 units
Reason for Recall
Listeria monocytogenes. The recalled Cotija cheese was repackaged into finished RTE Sprig and Sprout Ham and Cotija Torta Sandwich on Telera Roll.
Distribution
Domestic distribution only within state of Florida
Type: Voluntary: Firm initiated
Recall Initiated: 2024-02-09
Company
Melbourne, FL
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 51 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (COMPASS GROUP USA, INC.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does COMPASS GROUP USA, INC. have FDA actions?
This is the only FDA action we have on record for COMPASS GROUP USA, INC. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0910-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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