Sysco Imperial Thickened Dairy Drink. Mildly Thick Nectar Consistency. Pasteurized - Made with Grade A 2% Fat Milk, V
Summary
The FDA issued a Class I for Sysco Imperial Thickened Dairy Drink. Mildly Thick Nectar Consistency. Pasteur by Lyons Magnus, Inc. Reason: Findings and potential for Cronobacter sakazakii and Clostridium botulinum..
Details
Source
Food Recall
External ID
F-1630-2022
Action Date
2022-09-07
Status
Terminated
Category
food
Product Description
Sysco Imperial Thickened Dairy Drink. Mildly Thick Nectar Consistency. Pasteurized - Made with Grade A 2% Fat Milk, Vitamins A & D. Packaged in the following sized Tetra Pak containers: 1. 8 FL OZ (237 mL) UPC 0 74865-94549 3. Reorder # 0429274. 24 count case UPC 10074865945490. 2. 32 FL OZ (1 QT) 946mL UPC 7 34730-55615 4. Reorder # 4254284. 12 count case UPC 10734730556151. Refrigerate prior to serving. Shake well. Distributed by Sysco Corporation, Houston, Texas 77077.
Lot/Code Info: 1. 8 oz. cartons 0012 / Best By Date 11/6/2022; Lot Code 2212 / Best By Date 11/28/2022; Lot Code 3212 / Best By Date 11/29/2022; Lot Code 4212 / Best By Date 11/30/2022; . Lot Code 5712 / Best By Date 1/20/2023; Lot Code 6712 / Best By Date 1/21/2023; Lot Code 9902 / Best By Date 11/5/2022. EXPANED 8-10-2022 Lot Code 0502 / Best By Date 09/17/2022; Lot Code 1102 / Best By Date 08/09/2022; Lot Code 2102 / Best By Date 08/10/2022; Lot Code 3102 / Best By Date 08/11/2022; Lot Code 7602 / Best By Date 10/04/2022; Lot Code 8602 / Best By Date 10/05/2022. 2. 32 oz. cartons Lot Code 2512 / Best By Date 12/28/2022; Lot Code 3512 / Best By Date 12/29/2022; Lot Code 6902 / Best By Date 11/2/2022. EXPANDED 8-10-2022 Lot Code 1402 / Best By Date 09/08/2022; Lot Code 2402 / Best By Date 09/09/2022; Lot Code 2702 / Best By Date 10/09/2022; Lot Code 3402 / Best By Date 09/10/2022.
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-1630-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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