F-1612-2022 Class I Terminated

Recalled by Lyons Magnus, Inc — Fresno, CA

FDA food recall F-1612-2022 was initiated by Lyons Magnus, Inc on Jul 22, 2022 and is designated Class I. Reason for recall: Findings and potential for Cronobacter sakazakii and Clostridium botulinum. The recall status is terminated (terminated Jul 25, 2024). Affected quantity: 53,818,025 total units.

Recall Details

Product Type
Food
Report Date
Sep 7, 2022
Initiation Date
Jul 22, 2022
Termination Date
Jul 25, 2024
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
53,818,025 total units

Product Description

Lyons Ready Care Thickened Dairy Drink. Moderately Thick Honey Consistency. Pasteurized - Grade A Made with 2% Milk Fat Milk, Vitamins A & D Packaged in the following sized Tetra Pak containers: 1. 8 FL OZ (237 mL) UPC 0 45796-10044 2. Item 10044. 24 count case UPC 10045796100449. 2. 32 FL OZ (1 QT) 946mL UPC 0 45796-10046 6. Item 10046. 12 count case UPC 10045796100463. Refrigerate after opening. Manufactured for Lyons Magnus, Fresno, CA 93702.

Reason for Recall

Findings and potential for Cronobacter sakazakii and Clostridium botulinum.

Distribution Pattern

Nationwide

Code Information

1. 8 oz. containers: Lot Code 0012 / Best By Date 11/06/2022. EXPANDED 8-10-2022 Lot Code 0102 / Best By Date 08/08/2022. Lot Code 4102 / Best By Date 08/12/2022. Lot Code 5102 / Best By Date 08/13/2022. Lot Code 6402 / Best By Date 09/13/2022. Lot Code 7402 / Best By Date 09/14/2022. Lot Code 8202 / Best By Date 08/26/2022. 2. 32 oz. containers: Lot Code 4512 / Best By Date 12/30/2022; Lot Code 5512 / Best By Date 12/31/2022; Lot Code 5902 / Best By Date 11/01/2022. EXPANDED 8-10-2022 Lot Code 1702 / Best By Date 10/08/2022.

Source

Dataset
openFDA food recall enforcement reports
FDA record
This recall in openFDA (JSON)
Enforcement Report
Search FDA's Enforcement Report for F-1612-2022
openFDA file date
Oct 6, 2026
Loaded by RegDataLab
Oct 6, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it. FDA may have changed the recall since.