Ready Care Vanilla Shake (4 oz), UPC 10045796017334; Imperial Vanilla Shake (4 oz), UPC 00074865926836
Summary
The FDA issued a Class I for Ready Care Vanilla Shake (4 oz), UPC 10045796017334; Imperial Vanilla Shake (4 by Lyons Magnus LLC. Reason: Potential contamination with Listeria monocytogenes..
Details
Source
Food Recall
External ID
F-0655-2025
Action Date
2025-03-26
Status
Ongoing
Category
food
Product Description
Ready Care Vanilla Shake (4 oz), UPC 10045796017334; Imperial Vanilla Shake (4 oz), UPC 00074865926836
Lot/Code Info: BB codes: 022125 to 022126
Quantity Affected: 763,250 cases (50 or 75 cartons per case) Total
Reason for Recall
Potential contamination with Listeria monocytogenes.
Distribution
Distribution centers located throughout the U.S. and further distributed to sensitive populations located in long term care facilities, skilled nursing homes, hospitals, etc.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-02-21
Company
Fresno, CA
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 53 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Lyons Magnus LLC has 26 FDA actions in our database, including 26 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 (Lyons Magnus LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Lyons Magnus LLC have FDA actions?
Lyons Magnus LLC has 26 FDA actions in our database, including 26 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0655-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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