F-1602-2022 Class I Terminated

Recalled by Lyons Magnus, Inc — Fresno, CA

FDA food recall F-1602-2022 was initiated by Lyons Magnus, Inc on Jul 22, 2022 and is designated Class I. Reason for recall: Findings and potential for Cronobacter sakazakii and Clostridium botulinum. The recall status is terminated (terminated Jul 25, 2024). Affected quantity: 53,818,025 total units.

Recall Details

Product Type
Food
Report Date
Sep 7, 2022
Initiation Date
Jul 22, 2022
Termination Date
Jul 25, 2024
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
53,818,025 total units

Product Description

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.

Reason for Recall

Findings and potential for Cronobacter sakazakii and Clostridium botulinum.

Distribution Pattern

Nationwide

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.

Source

Dataset
openFDA food recall enforcement reports
FDA record
This recall in openFDA (JSON)
Enforcement Report
Search FDA's Enforcement Report for F-1602-2022
openFDA file date
Oct 6, 2026
Loaded by RegDataLab
Oct 6, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it. FDA may have changed the recall since.