kate farms Nutrition Shake, Chocolate. 11 fl oz (325 mL) UPC 8 11112-03060 7. 12 count case UPC 00811112030614. Shak
Summary
The FDA issued a Class I for kate farms Nutrition Shake, Chocolate. 11 fl oz (325 mL) UPC 8 11112-03060 7. by Lyons Magnus, Inc. Reason: Findings and potential for Cronobacter sakazakii and Clostridium botulinum..
Details
Source
Food Recall
External ID
F-1668-2022
Action Date
2022-09-07
Status
Terminated
Category
food
Product Description
kate farms Nutrition Shake, Chocolate. 11 fl oz (325 mL) UPC 8 11112-03060 7. 12 count case UPC 00811112030614. Shake Well. After opening, refrigerate and use within 4 days. Made for Kate Farms, Inc., 101 Innovation Place, Santa Barbara, CA 93708
Lot/Code Info: EXPANDED 8-10-2022 Lot Code 0602 / Best By Date 03/01/2023 Lot Code 1602 / Best By Date 03/02/2023 Lot Code 2621 / Best By Date 09/19/2022 Lot Code 2821 / Best By Date 10/09/2022 Lot Code 1821 / Best By Date 10/08/2022 Lot Code 6102 / Best By Date 01/16/2023 Lot Code 7031 / Best By Date 11/03/2022 Lot Code 7102 / Best By Date 01/17/2023
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-1668-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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