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Class ITerminated in FDA datasetRecall initiated Jul 22, 2022

Glucerna original Rich Chocolate Shake, 8 FL OZ (237 mL). Delicious Snack or Small Meal…

Recalling firm: Lyons Magnus, Inc

Why it was recalled

Findings and potential for Cronobacter sakazakii and Clostridium botulinum.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Jul 25, 2024.

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Compare the exact product and package details with the label you have.

ProductGlucerna original Rich Chocolate Shake, 8 FL OZ (237 mL). Delicious Snack or Small Meal Replacement. UPC 0 70074-68565 6. Sold in 24 count case, UPC Case 0070074685649. 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.
Package size8 FL OZ
UPC070074685656

FDA code information

Lot Code 400254X00 / Best By Date 08/01/2023. Lot Code 400264X00 / Best By Date 08/01/2023 Lot Code 400274X00 / Best By Date 08/01/2023 Lot Code 410364X00 / Best By Date 09/01/2023. EXPANDED 8-10-2022 Lot Code 390184X00 / Best By Date 07/01/2023

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Full FDA record and distribution details

Original product description

Glucerna original Rich Chocolate Shake, 8 FL OZ (237 mL). Delicious Snack or Small Meal Replacement. UPC 0 70074-68565 6. Sold in 24 count case, UPC Case 0070074685649. 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.

Extracted codes and context

TypeCode / valueContext
UPC070074685656late Shake, 8 FL OZ (237 mL). Delicious Snack or Small Meal Replacement. UPC 0 70074-68565 6. Sold in 24 count case, UPC Case 0070074685649. Shake Well. Serve cold. Refrigerate after opening. Manufactured

Original FDA recall reason

Findings and potential for Cronobacter sakazakii and Clostridium botulinum.

Recall details

Recall number
F-1600-2022
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-1600-2022

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

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