Lyons Ready Care Thickened Dairy Drink. Moderately Thick Honey Consistency. Pasteurized - Grade A Made with 2% Milk F
Summary
The FDA issued a Class I for Lyons Ready Care Thickened Dairy Drink. Moderately Thick Honey Consistency. Pa by Lyons Magnus, Inc. Reason: Findings and potential for Cronobacter sakazakii and Clostridium botulinum..
Details
Source
Food Recall
External ID
F-1612-2022
Action Date
2022-09-07
Status
Terminated
Category
food
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.
Lot/Code Info: 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.
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-1612-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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