CLASS IFood recall · Reported 7 Sep 2022 · FDA Enforcement Report
pirq Plant Protein Super Foods, Very Strawberry Drink recalled
Lyons Magnus is recalling pirq Plant Protein Super Foods, Very Strawberry Drink, Almonds, Curcumin, Maca, distributed nationwide in the US. The recall was initiated on 22 Jul 2022 and the FDA has classified it as Class I.
Check your package
Lot, batch or date codes1. 12 count case Lot Code 4412 / Best By Date 07/23/2023; Lot Code 5412 / Best By Date 07/24/2023; Lot Code 7012 / Best By Date 06/16/2023; Lot Code 8012 / Best By Date 06/17/2023. EXPANDED 8-10-2022 Lot Code 4502 / Best By Date 04/24/2023. 2. 4 count case Lot Code 7012 / Best By Date 06/16/2023.
Quantity recalled53,818,025 total units
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Findings and potential for Cronobacter sakazakii and Clostridium botulinum.
Product as listed by the FDA
pirq Plant Protein Super Foods, Very Strawberry Drink, Almonds, Curcumin, Maca. 11 FL OZ (325ML). UPC 8 57690-00830 0. Packaged in the following configurations: 1. 12 count case UPC 857690008331. 2. 4 count wrap UPC 857690008317. Chill it, Shake it. Do not Freeze. Refrigerate after Opening. Distributed by: MS Brands Inc., Irvine, CA 92602
Findings and potential for Cronobacter sakazakii and Clostridium botulinum.
Which lots are affected?
1. 12 count case Lot Code 4412 / Best By Date 07/23/2023; Lot Code 5412 / Best By Date 07/24/2023; Lot Code 7012 / Best By Date 06/16/2023; Lot Code 8012 / Best By Date 06/17/2023. EXPANDED 8-10-2022 Lot Code 4502 / Best By Date 04/24/2023. 2. 4 count case Lot Code 7012 / Best By Date 06/16/2023.
Where was it sold?
Nationwide
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.