Glucerna original Homemade Vanilla Shake, 8 FL OZ (237 mL). Delicious Snack or Small Meal Replacement. UPC 0 70074-685
Summary
The FDA issued a Class I for Glucerna original Homemade Vanilla Shake, 8 FL OZ (237 mL). Delicious Snack or by Lyons Magnus, Inc. Reason: Findings and potential for Cronobacter sakazakii and Clostridium botulinum..
Details
Source
Food Recall
External ID
F-1602-2022
Action Date
2022-09-07
Status
Terminated
Category
food
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.
Lot/Code Info: 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.
Quantity Affected: 53,818,025 total units
Reason for Recall
Findings and potential for Cronobacter sakazakii and Clostridium botulinum.
Distribution
Nationwide
Type: Voluntary: Firm initiated
Recall Initiated: 2022-07-22
Company
Fresno, CA
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 111 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Lyons Magnus, Inc has 78 FDA actions in our database, including 78 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Lyons Magnus, Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Lyons Magnus, Inc have FDA actions?
Lyons Magnus, Inc has 78 FDA actions in our database, including 78 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1602-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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