pirq Plant Protein Super Foods, Caramel Coffee Drink, Almonds, Curcumin, Maca. 11 FL OZ (325ML). UPC 8 57690-00808 9.
Summary
The FDA issued a Class I for pirq Plant Protein Super Foods, Caramel Coffee Drink, Almonds, Curcumin, Maca. by Lyons Magnus, Inc. Reason: Findings and potential for Cronobacter sakazakii and Clostridium botulinum..
Details
Source
Food Recall
External ID
F-1619-2022
Action Date
2022-09-07
Status
Terminated
Category
food
Product Description
pirq Plant Protein Super Foods, Caramel Coffee Drink, Almonds, Curcumin, Maca. 11 FL OZ (325ML). UPC 8 57690-00808 9. Packaged in the following configurations: 1. 12 count case UPC 857690008140. 2. 4 count wrap UPC 857690008263. Chill it, Shake it. Do not Freeze. Refrigerate after Opening. Distributed by: MS Brands Inc., Irvine, CA 92602
Lot/Code Info: 1. 12 count case Lot Code 8412 / Best By Date 07/27/2023; Lot Code 9412 / Best By Date 07/28/2023. EXPANDED 8-10-2022 Lot Code 0202 / Best By Date 01/15/2023. Lot Code 0902 / Best By Date 05/30/2023. Lot Code 0921 / Best By Date 10/12/2022. Lot Code 1202 / Best By Date 01/16/2023. Lot Code 5131 / Best By Date 11/06/2022. Lot Code 6131 / Best By Date 11/07/2022. Lot Code 7502 / Best By Date 04/27/2023. Lot Code 8502 / Best By Date 04/28/2023. Lot Code 9221 / Best By Date 08/12/2022. Lot Code 9802 / Best By Date 05/29/2023. Lot Code 9821 / Best By Date 10/11/2022. 2. 4 count case Lot Code 8412 / Best By Date 7/27/2023 EXPANDED 8-10-2022 Lot Code 0202 / Best By Date 01/20/2023. Lot Code 0902 / Best By Date 05/30/2023. Lot Code 5131 / Best By Date 11/11/2022. Lot Code 6131 / Best By Date 11/12/2022.
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-1619-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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