CLASS IFood recall · Reported 7 Sep 2022 · FDA Enforcement Report
Sysco Imperial Med Plus NSA 1.7 Vanilla Nutritional Drink recalled
Lyons Magnus is recalling Sysco Imperial Med Plus NSA 1.7 Vanilla Nutritional Drink, distributed nationwide in the US. The recall was initiated on 22 Jul 2022 and the FDA has classified it as Class I.
Check your package
Lot, batch or date codesLot Code 1312 / Best By Date 2/5/2023; Lot Code 1902 / Best By Date 12/27/2022. EXPANDED 8-10-2022 Lot Code 0902 / Best By Date 12/26/2022 Lot Code 1431 / Best By Date 09/03/2022 Lot Code 7131 / Best By Date 08/10/2022 Lot Code 8102 / Best By Date 10/15/2022
Quantity recalled53,818,025 total units
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Findings and potential for Cronobacter sakazakii and Clostridium botulinum.
Product as listed by the FDA
Sysco Imperial Med Plus NSA 1.7 Vanilla Nutritional Drink. High Calorie, High Protein. Mildly Thick Nectar Consistency. 32 FL OZ (1 QT) 946mL UPC 7 34730-31074 9. Reorder # 0794018. 12 count case UPC 10734730310746. Refrigerate prior to serving. Shake well. Refrigerate after opening and use within 3 days. Distributed by Sysco Corporation, Houston, Texas 77077.
Findings and potential for Cronobacter sakazakii and Clostridium botulinum.
Which lots are affected?
Lot Code 1312 / Best By Date 2/5/2023; Lot Code 1902 / Best By Date 12/27/2022. EXPANDED 8-10-2022 Lot Code 0902 / Best By Date 12/26/2022 Lot Code 1431 / Best By Date 09/03/2022 Lot Code 7131 / Best By Date 08/10/2022 Lot Code 8102 / Best By Date 10/15/2022
Where was it sold?
Nationwide
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.