CLASS IFood recall · Reported 7 Sep 2022 · FDA Enforcement Report
Glucerna original Creamy Strawberry Shake recalled by Lyons Magnus
Lyons Magnus is recalling Glucerna original Creamy Strawberry 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 400244X00 / Best By Date 08/01/2023; Lot Code 410354X00 / Best By Date 09/01/2023. EXPANDED 8-10-2022 Lot Code 390154X00 / Best By Date 07/01/2023; Lot Code 390164X00 / Best By Date 07/01/2023; Lot Code 390174X00 / Best By Date 07/01/2023.
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.
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
Glucerna original Creamy Strawberry Shake, 8 FL OZ (237 mL). Delicious Snack or Small Meal Replacement. UPC 0 70074-68567 0. Sold as 24 count case, Case UPC 0070074685663. Shake Well. Serve cold. Refrigerate after opening. Manufactured for: Abbott Nutrition, Abbott Laboratories, Columbus, Ohio 43219. Can be sold in 24 - 8 oz Cartons or individual 8 oz Tetra Pak containers.
Findings and potential for Cronobacter sakazakii and Clostridium botulinum.
Which lots are affected?
Lot Code 400244X00 / Best By Date 08/01/2023; Lot Code 410354X00 / Best By Date 09/01/2023. EXPANDED 8-10-2022 Lot Code 390154X00 / Best By Date 07/01/2023; Lot Code 390164X00 / Best By Date 07/01/2023; Lot Code 390174X00 / Best By Date 07/01/2023.
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 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.