CLASS I Food recall · Reported 7 Sep 2022 · FDA Enforcement Report

MRE Vanilla Protein Shake recalled by Lyons Magnus

Lyons Magnus is recalling MRE Vanilla Protein Shake, distributed nationwide in the US. The recall was initiated on 22 Jul 2022 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot Code 0112 / Best By Date 04/20/2023; Lot Code 1112 / Best By Date 04/21/2023; Lot Code 6612 / Best By Date 06/15/2023; Lot Code 7612 / Best By Date 06/16/2023. EXPANDED 8-10-2022 Lot Code 2421 / Best By Date 08/30/2022; Lot Code 3421 / Best By Date 08/31/2022; Lot Code 4421 / Best By Date 09/01/2022.
Quantity recalled53,818,025 total units

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-1629-2022
FDA event ID
90667
Recalling firm
Lyons Magnus, Fresno, CA
Brand
Mre
Classification
Class I
Status
Terminated
Recall initiated
22 Jul 2022
FDA classified
30 Aug 2022
Reported
7 Sep 2022
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Botulism
Product category
Protein Powder

Timeline

22 Jul 2022Recall initiated by company
30 Aug 2022Classified by FDA+39 days
7 Sep 2022Published in enforcement report+8 days

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

Reason for recall

Findings and potential for Cronobacter sakazakii and Clostridium botulinum.

Product as listed by the FDA

MRE Vanilla Protein Shake. Whole Food Protein High protein shake. 11 FL OZ (325mL) Tetra Pak. UPC 8 10044-57390 9. 4-count case UPC 810044573954. Refrigerate after Opening. Distributed by: Redcon1, LLC, 701 Park of Commerce Blvd, Boca Raton, FL 33487

Where it was distributed

Nationwide

Nationwide

Questions about this recall

Is MRE Vanilla Protein Shake recalled?

Yes. Lyons Magnus recalled MRE Vanilla Protein Shake on 22 Jul 2022. The recall is Class I and its status is Terminated. Recall number F-1629-2022.

Why was it recalled?

Findings and potential for Cronobacter sakazakii and Clostridium botulinum.

Which lots are affected?

Lot Code 0112 / Best By Date 04/20/2023; Lot Code 1112 / Best By Date 04/21/2023; Lot Code 6612 / Best By Date 06/15/2023; Lot Code 7612 / Best By Date 06/16/2023. EXPANDED 8-10-2022 Lot Code 2421 / Best By Date 08/30/2022; Lot Code 3421 / Best By Date 08/31/2022; Lot Code 4421 / Best By Date 09/01/2022.

Where was it sold?

Nationwide

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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