Item # 407034, Don Pancho Fiesta 3 Pack Everything Sauce. Each pack consists of Cilantro Lime Crema, Baja-Style Crema,
Summary
The FDA issued a Class I for Item # 407034, Don Pancho Fiesta 3 Pack Everything Sauce. Each pack consists of 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-1087-2024
Action Date
2024-03-27
Status
Terminated
Category
food
Product Description
Item # 407034, Don Pancho Fiesta 3 Pack Everything Sauce. Each pack consists of Cilantro Lime Crema, Baja-Style Crema, Chipotle Crema. 3/12oz glass bottles per pack, 6 packs per case. UPC on 3-pack box: 0 71117 00741 1.
Lot/Code Info: Lot 170255, Use By 3/11/2024 Lot 170292, Use By 3/11/2024 Lot 170684, Use By 3/11/2024 Lot 170686, Use By 3/15/2024 Lot 170686, Use By 3/23/2024 Lot 170686, Use By 3/24/2024 Lot 170686, Use By 3/26/2024 Lot 170984, Use By 3/11/2024 Lot 170984, Use By 3/12/2024 Lot 170984, Use By 3/15/2024 Lot 171233, Use By 3/15/2024
Quantity Affected: 4319 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-1087-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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