Class ITerminated in FDA datasetRecall initiated Jul 22, 2022

Aloha Organic Protein Drink, Iced Coffee 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, Iced Coffee Plant-based protein. Net 11 FL OZ (330 mL) Tetra Pak container UPC 8 42096-11238 6. Sold as 4 count package wrap with UPC 842096122385. Shake Well. Best Chilled. Manufactured for: Aloha, Littleton, CO 80127
Package size11 FL OZ
UPC842096112386, 842096122385

FDA code information

Lot Code 0412 / Best By Date 07/19/2023 Lot Code 9312 / Best By Date 07/18/2023. EXPANDED 8-10-2022 Lot Code 1702 / Best By Date 05/11/2023. Lot Code 8821 / Best By Date 12/14/2022. Lot Code 9821 / Best By Date 12/15/2022.

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, Iced Coffee Plant-based protein. Net 11 FL OZ (330 mL) Tetra Pak container UPC 8 42096-11238 6. Sold as 4 count package wrap with UPC 842096122385. Shake Well. Best Chilled. Manufactured for: Aloha, Littleton, CO 80127

Extracted codes and context

TypeCode / valueContext
UPC842096112386Iced Coffee Plant-based protein. Net 11 FL OZ (330 mL) Tetra Pak container UPC 8 42096-11238 6. Sold as 4 count package wrap with UPC 842096122385. Shake Well. Best Chilled. Manufactured for: Aloha, Little
UPC842096122385Tetra Pak container UPC 8 42096-11238 6. Sold as 4 count package wrap with UPC 842096122385. 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-1606-2022
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 total units
Location
Fresno, CA, United States
Initiation type
Voluntary: Firm initiated
Notification
Telephone

Where it was distributed

Nationwide

FDA source record · F-1606-2022

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

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