Sysco Imperial Thickened Dairy Drink. Mildly Thick Nectar Consistency. Past...

FDA Recall #F-1630-2022 — Class I — July 22, 2022

Recall Summary

Recall NumberF-1630-2022
Date InitiatedJuly 22, 2022
ClassificationClass I
StatusTerminated
TypeVoluntary: Firm initiated
Product TypeFood

Recalling Firm

FirmLyons Magnus, Inc
LocationFresno, CA

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.

Reason for Recall

Findings and potential for Cronobacter sakazakii and Clostridium botulinum.

Classification

Class I — 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.

Distribution Pattern

Nationwide

Product Quantity

53,818,025 total units

Product Codes / Lot Numbers

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.

What Should You Do?

Stop consuming this product immediately. Check your home for the recalled item and dispose of it safely. If you experienced a health issue after consuming this product, contact your doctor and report it to the FDA MedWatch.

Frequently Asked Questions

Stop consuming the product immediately and do not donate or give it to others. Check the recall notice above for specific disposal or return instructions. Many food recalls ask you to throw the product away and retain the packaging for a possible refund from the retailer. If you purchased it online, check your order history — some retailers send recall notifications directly to customers. You do not need a receipt to report an issue or seek a refund; the fact of purchase is typically sufficient.

In most cases, yes. Retailers are typically notified to accept returns of recalled products and issue refunds, regardless of whether you have a receipt. Check with the store where you purchased the item. Some manufacturers also offer direct refunds — contact the recalling firm using the information in the official recall notice. If you purchased the product online, contact the retailer's customer service with your order number. In either case, you generally do not need original packaging, though retaining the product label with the lot code or UPC can speed up the process.

Report foodborne illnesses and adverse food reactions to the FDA through the MedWatch Safety Reporting Portal at FDA.gov, or by calling 1-800-332-1088. You can also report issues directly to the FDA's Safety Reporting Portal at SafetyReporting.hhs.gov. If you believe there is an immediate public health risk, contact your local health department. Your report helps the FDA identify contamination patterns, initiate recalls faster, and protect other consumers from the same hazard. Include as much detail as possible: the product name, lot code, purchase date and location, and a description of your symptoms or findings.

The FDA assigns a status to each recall action throughout its lifecycle. "Ongoing" means the recall is active — the firm is still working to remove the product from commerce and notify consumers. "Completed" means the recall strategy has been implemented and the FDA has determined that the recalling firm has taken all appropriate steps to remove the product. "Terminated" means the FDA has reviewed the results and concluded the recall is complete. Even if a recall is marked as completed or terminated, you should still discard any recalled products you find at home — the recall status refers to the firm's compliance actions, not the safety of product still in consumers' possession.