Class ITerminated in FDA datasetRecall initiated Jul 22, 2022

Aloha Organic Protein Drink, Coconut Plant-based protein. Net 11 FL OZ (330 mL) Tetra Pak…

Recalling firm: Lyons Magnus, Inc

Why it was recalled

Findings and potential for Cronobacter sakazakii and Clostridium botulinum.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Jul 25, 2024.

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Compare the exact product and package details with the label you have.

ProductAloha Organic Protein Drink, Coconut Plant-based protein. Net 11 FL OZ (330 mL) Tetra Pak container UPC 8 42096-11237 9. Sold in 4 count package wrap with UPC 842096122378. Shake Well. Best Chilled. Manufactured for: Aloha, Littleton, CO 80127
Package size11 FL OZ
UPC842096112379, 842096122378

FDA code information

Lot Code 7312 / Best By Date 7/11/2023 EXPANDED 8-10-2022 Lot Code 1302 / Best By Date 03/27/2023. Lot Code 2221 / Best By Date 10/04/2022. Lot Code 5431 / Best By Date 02/04/2023. Lot Code 5821 / Best By Date 12/06/2022.

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

Aloha Organic Protein Drink, Coconut Plant-based protein. Net 11 FL OZ (330 mL) Tetra Pak container UPC 8 42096-11237 9. Sold in 4 count package wrap with UPC 842096122378. Shake Well. Best Chilled. Manufactured for: Aloha, Littleton, CO 80127

Extracted codes and context

TypeCode / valueContext
UPC842096112379nk, Coconut Plant-based protein. Net 11 FL OZ (330 mL) Tetra Pak container UPC 8 42096-11237 9. Sold in 4 count package wrap with UPC 842096122378. Shake Well. Best Chilled. Manufactured for: Aloha, Littl
UPC842096122378etra Pak container UPC 8 42096-11237 9. Sold in 4 count package wrap with UPC 842096122378. Shake Well. Best Chilled. Manufactured for: Aloha, Littleton, CO 80127

Original FDA recall reason

Findings and potential for Cronobacter sakazakii and Clostridium botulinum.

Recall details

Recall number
F-1604-2022
Event ID
90667
FDA status
Terminated
Initiated
Jul 22, 2022
Reported
Sep 7, 2022
Classified
Aug 30, 2022
Terminated
Jul 25, 2024
Quantity
53,818,025 units total
Location
Fresno, CA, United States
Initiation type
Voluntary: Firm initiated
Notification
Telephone

Where it was distributed

Nationwide

FDA source record · F-1604-2022

Data updated September 16, 2026. View official FDA data ↗

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