CLASS I ONGOING Food recall · Reported 26 Mar 2025 · FDA Enforcement Report

Ready Care Strawberry Shake Plus recalled by Lyons Magnus

Lyons Magnus is recalling Ready Care Strawberry Shake Plus, distributed nationwide in the US. The recall was initiated on 21 Feb 2025 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesBB codes: 022125 to 022126
Quantity recalled763,250 cases (50 or 75 cartons per case) Total

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0661-2025
FDA event ID
96376
Recalling firm
Lyons Magnus, Fresno, CA
Classification
Class I
Status
Ongoing
Recall initiated
21 Feb 2025
FDA classified
20 Mar 2025
Reported
26 Mar 2025
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Listeria
Product category
Strawberries

Timeline

21 Feb 2025Recall initiated by company
20 Mar 2025Classified by FDA+27 days
26 Mar 2025Published in enforcement report+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Potential contamination with Listeria monocytogenes.

Listeria monocytogenes can grow at refrigerator temperatures. Infection is most dangerous for pregnant women, newborns, older adults and people with weakened immune systems. Symptoms can appear up to 70 days after eating contaminated food.

Product as listed by the FDA

Ready Care Strawberry Shake Plus (4 oz), UPC 10045796017495

Where it was distributed

Distribution centers located throughout the U.S. and further distributed to sensitive populations located in long term care facilities, skilled nursing homes, hospitals, etc.

Nationwide

Questions about this recall

Is Ready Care Strawberry Shake Plus recalled?

Yes. Lyons Magnus recalled Ready Care Strawberry Shake Plus on 21 Feb 2025. The recall is Class I and its status is Ongoing. Recall number F-0661-2025.

Why was it recalled?

Potential contamination with Listeria monocytogenes.

Which lots are affected?

BB codes: 022125 to 022126

Where was it sold?

Distribution centers located throughout the U.S. and further distributed to sensitive populations located in long term care facilities, skilled nursing homes, hospitals, etc.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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