Rojo Black Bean 6 Layer Dip packaged in 20oz PET plastic containers, sold in sleeve with two containers per sleeve. 12 s
Summary
The FDA issued a Class I for Rojo Black Bean 6 Layer Dip packaged in 20oz PET plastic containers, sold in sle by Lakeview Farms LLC. Reason: Potential contamination of Listeria monocytogenes.
Details
Source
Food Recall
External ID
F-1003-2024
Action Date
2024-03-06
Status
Terminated
Category
food
Product Description
Rojo Black Bean 6 Layer Dip packaged in 20oz PET plastic containers, sold in sleeve with two containers per sleeve. 12 sleeves per case.
Lot/Code Info: Lot Codes/Best By Dates: Feb 06 2024, Feb 14 2024, Feb 16 2024, Feb 21 2024, Feb 23 2024, Feb 29 2024, Mar 02 2024, Mar 07 2024, Mar 09 2024, Mar 14 2024, Mar 21 2024, Mar 22 2024 Product Nos. 008292 (USA) 001842 (Canada)
Quantity Affected: US - 7350 cases; Canada - 2584 cases
Reason for Recall
Potential contamination of Listeria monocytogenes
Distribution
Alabama/Alaska/ Florida/Georgia/Idaho/Mississippi/Montana/North Carolina/Oregon/South Carolina/Tennessee/Utah/Washington
Type: Voluntary: Firm initiated
Recall Initiated: 2024-02-06
Company
Delphos, OH
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 128 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Lakeview Farms LLC has 4 FDA actions in our database, including 4 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 (Lakeview Farms LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Lakeview Farms LLC have FDA actions?
Lakeview Farms LLC has 4 FDA actions in our database, including 4 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1003-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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