The Recall Desk
Agency classClass IOur severity:CriticalFDA (Food)·F-1634-2022·Announced 2022-09-07

Nutritional Drink Recalled for Potential Cronobacter and Botulinum Contamination

Sysco Imperial Med Plus 2.0 nutritional drink is recalled nationwide for potential contamination with Cronobacter sakazakii and Clostridium botulinum. The FDA classified this as Class I.

The agency’s classification

FDA (Food): Class I

Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.

This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work

What this means for you

Our assessment, not the agency’s: severity 5/5 (Critical).

Highest-severity recall. The hazard can cause serious injury or death. Stop using the product now and follow the agency's instructions.

Our severity reasoning: FDA Class I classification indicates the most serious hazard category. The potential for Cronobacter sakazakii and Clostridium botulinum contamination in a consumed product presents critical health risks.

Plain-English summary

Sysco Imperial Med Plus 2.0, a butter pecan nutritional drink, is being recalled. The product is a high-calorie, high-protein drink distributed nationwide in 32 fl oz bottles.

The recall is due to potential contamination with Cronobacter sakazakii and Clostridium botulinum. The FDA classified this as a Class I recall, the most serious designation.

The recall affects 53,818,025 units with multiple lot codes and best-by dates ranging from August 2022 to March 2023.

Consumers with this product should discontinue use immediately. Anyone who has consumed the product should contact a healthcare provider if experiencing symptoms.

The recalled product

Product
Sysco Imperial Med Plus 2.0 butter Pecan Nutritional Drink. High Calorie, High Protein. Mildly Thick Nectar Consistency. 32 FL OZ (1 QT) 946mL UPC 0 74865-92732 1. Reorder # 0108936. 12 count case UPC 10074865927328. Refrigerate prior to serving. Shake well.…
Manufacturer
Lyons Magnus, Inc
Affected units
53,818,025

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (3)

  • Lot Code 0012 / Best By Date 1/5/2023
  • Lot Code 1412 / Best By Date 2/15/2023
  • Lot Code 9512 / Best By Date 3/5/2023

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 77 recalled by Lyons Magnus, Inc under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 77 products in this recall →

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