Sysco Imperial Med Plus 2.0 Vanilla Nutritional Drink. High Calorie, High Protein. Mildly Thick Nectar Consistency.
Summary
The FDA issued a Class I for Sysco Imperial Med Plus 2.0 Vanilla Nutritional Drink. High Calorie, High Prote by Lyons Magnus, Inc. Reason: Findings and potential for Cronobacter sakazakii and Clostridium botulinum..
Details
Source
Food Recall
External ID
F-1632-2022
Action Date
2022-09-07
Status
Terminated
Category
food
Product Description
Sysco Imperial Med Plus 2.0 Vanilla Nutritional Drink. High Calorie, High Protein. Mildly Thick Nectar Consistency. 32 FL OZ (1 QT) 946mL UPC 0 74865-92730 7. Reorder # 0108910. 12 count case UPC 10074865927304. Refrigerate prior to serving. Shake well. Refrigerate after opening and use within 3 days. Distributed by Sysco Corporation, Houston, Texas 77077.
Lot/Code Info: Lot Code 2312 / Best By Date 2/6/2023; Lot Code 3312 / Best By Date 2/7/2023; Lot Code 7112 / Best By Date 1/22/2023; Lot Code 8112 / Best By Date 1/23/2023; Lot Code 8612 / Best By Date 3/14/2023. EXPANDED 8-10-2022 Lot Code 0431 / Best By Date 09/02/2022, Lot Code 0702 / Best By Date 12/06/2022. Lot Code 5002 / Best By Date 10/02/2022. Lot Code 5302 / Best By Date 11/01/2022. Lot Code 6002 / Best By Date 10/03/2022. Lot Code 6302 / Best By Date 11/02/2022. Lot Code 7131 / Best By Date 08/10/2022. Lot Code 7302 / Best By Date 11/03/2022. Lot Code 7331 / Best By Date 08/30/2022. Lot Code 8131 / Best By Date 08/11/2022. Lot Code 8602 / Best By Date 12/04/2022. Lot Code 9131 / Best By Date 08/12/2022. Lot Code 9331 / Best By Date 09/01/2022. Lot Code 9602 / Best By Date 12/05/2022.
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-1632-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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