Check the Batch
Class ITerminated in FDA datasetJul 22, 2022

Glucerna original Homemade Vanilla Shake, 8 FL OZ (237 mL). Delicious Snack or Small Meal Replacement.

Recalling firm: Lyons Magnus, Inc

Why it was recalled

Findings and potential for Cronobacter sakazakii and Clostridium botulinum.

Check the codes ↓

The exact product

Glucerna original Homemade Vanilla Shake, 8 FL OZ (237 mL). Delicious Snack or Small Meal Replacement. UPC 0 70074-68563 2. Sold in 24 count case, Case UPC 0070074685625. 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.

snacks

Check the codes

Compare these FDA-provided codes, lot numbers or dates with the product you have.

Match the product, size and code together. A similar name alone does not identify your batch.

Original FDA code information

Lot Code 400194X00 / Best By Date 08/01/2023; Lot Code 400204X00 / Best By Date 08/01/2023; Lot Code 400214X00 / Best By Date 08/01/2023; Lot Code 400224X00 / Best By Date 08/01/2023; Lot Code 400234X00 / Best By Date 08/01/2023; Lot Code 410294X00 / Best By Date 09/01/2023; Lot Code 410304X00 / Best By Date 09/01/2023; Lot Code 410314X00 / Best By Date 09/01/2023; Lot Code 410334X00 / Best By Date 09/01/2023; Lot Code 410344X00 / Best By Date 09/01/2023. EXPANDED 08/10/2022 Lot Code 390124X00 / Best By Date 07/01/2023; Lot Code 390134X00 / Best By Date 07/01/2023; Lot Code 390144X00 / Best By Date 07/01/2023.

TypeCode / valueContext
UPC070074685632nilla Shake, 8 FL OZ (237 mL). Delicious Snack or Small Meal Replacement. UPC 0 70074-68563 2. Sold in 24 count case, Case UPC 0070074685625. Shake Well. Serve cold. Refrigerate after opening. Manufactured

Recall details

Recall number
F-1602-2022
Event ID
90667
FDA status
Terminated
Initiated
Jul 22, 2022
Reported
Sep 7, 2022
Classified
Aug 30, 2022
Terminated
Jul 25, 2024
Quantity
53,818,025 total units
Location
Fresno, CA, United States
Initiation type
Voluntary: Firm initiated
Notification
Telephone

Where it was distributed

Nationwide

FDA source record · F-1602-2022

Data updated September 16, 2026. View official FDA data ↗

A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.