FCF Item 406957, Costco Item # 1744097, Club COSTCO SW Wrap Kit, Costco Service Deli, 2/8.15 lbs. Net Wt. 16.31 lbs., UP
Summary
The FDA issued a Class I for FCF Item 406957, Costco Item # 1744097, Club COSTCO SW Wrap Kit, Costco Service by Reser's Fine Foods, Inc.. Reason: Listeria monocytogenes. The recalled Cotija cheese was repackaged into finished wholesale and retail RTE products..
Details
Source
Food Recall
External ID
F-1090-2024
Action Date
2024-03-27
Status
Terminated
Category
food
Product Description
FCF Item 406957, Costco Item # 1744097, Club COSTCO SW Wrap Kit, Costco Service Deli, 2/8.15 lbs. Net Wt. 16.31 lbs., UPC 0 13454 38424 4. Costco assembled and sold product as Southwest Wrap with Sauce, item #29433.
Lot/Code Info: Use By dates range: 12/10/2023 - 12/29/2023 01/04/2024 - 03/15/2024 Lot numbers: 164746 165267 165268 165269 165270 165744 165745 165746 166213 166214 166215 166774 166776 166778 166821 167072 167235 167345 167671 167672 168088 168117 168543 168545 168546 168855 168985 168986 169158 169220 169388 169390 169436 169684 169774 169775 169783 169978 170237 170238 170240 170521 170673 170674 170982 171123 171124 171125 171609
Quantity Affected: 81,682 cases
Reason for Recall
Listeria monocytogenes. The recalled Cotija cheese was repackaged into finished wholesale and retail RTE products.
Distribution
Distributed in CA, CT, FL, ID, IL, MD, MT, NJ, NV, OR, PA, SD, TX, UT, VA, and WA.
Type: Voluntary: Firm initiated
Recall Initiated: 2024-02-06
Company
Beaverton, OR
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 41 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Reser's Fine Foods, Inc. has 62 FDA actions in our database, including 62 recalls.
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 (Reser's Fine Foods, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Reser's Fine Foods, Inc. have FDA actions?
Reser's Fine Foods, Inc. has 62 FDA actions in our database, including 62 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1090-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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