Sysco Imperial Med Plus 2.0 Vanilla Nutritional Drink. High Calorie, High Protein. Mildly Thick…
Recalling firm: Lyons Magnus, Inc
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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074865927307FDA code information
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.
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Full FDA record and distribution details
Original 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.
Extracted codes and context
| Type | Code / value | Context |
|---|---|---|
| UPC | 074865927307 | 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 aft |
Original FDA recall reason
Findings and potential for Cronobacter sakazakii and Clostridium botulinum.
Recall details
- Recall number
- F-1632-2022
- 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
Data updated September 16, 2026. View official FDA data ↗
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