Premier Protein Cafe Latte High protein shake. 11 FL OZ (325mL). Packaged in the following configurations: 1.
Summary
The FDA issued a Class I for Premier Protein Cafe Latte High protein shake. 11 FL OZ (325mL). Packaged by Lyons Magnus, Inc. Reason: Findings and potential for Cronobacter sakazakii and Clostridium botulinum..
Details
Source
Food Recall
External ID
F-1625-2022
Action Date
2022-09-07
Status
Terminated
Category
food
Product Description
Premier Protein Cafe Latte High protein shake. 11 FL OZ (325mL). Packaged in the following configurations: 1. Carton UPC 6 43843-71668 6 packed in 4 count wrap UPC 643843716679. 2. Carton UPC 6 43843-71665 5 packed in 18 count case UPC 643843718567. Shake Well and Serve Cold. Refrigerate after Opening. Distributed by: Premier Nutrition, Emeryville, CA 94608. EXPANDED 8-10-2022 3. Carton UPC 6 43843-71668 6 Packed in 12 count case UPC 643843716624.
Lot/Code Info: 1. 4 count case Lot Code 3212/2123BT / Best By Date 7/1/2023; Lot Code 4212/2124BT / Best By Date 7/2/2023; Lot Code 5212/2125BT / Best By Date 7/3/2023; Lot Code 62122126BT / Best By Date 7/4/2023; Lot Code 7212/2127BT / Best By Date 7/5/2023. 2. 18 count case Lot Code 8212/2128BT / Best By Date 7/6/2023. EXPANDED 8-10-2022 3, 12 count case Lot Code 0402 / 2040BT / Best By Date 4/9/2023.
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-1625-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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