Lyons Magnus, Inc Recall: Findings and potential for Cronobacter sakazakii and Clostridium botulinum.

🇺🇸 United States

1. July 22, 2022 - Recall initiated
2. September 7, 2022 - Reported by source
3. July 25, 2024 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-1605-2022

Event ID

90667

Status

Terminated

Classification

Class I

Company

Lyons Magnus, Inc

Product description

Aloha Organic Protein Drink, Vanilla Plant-based protein. Net 11 FL OZ (330 mL) Tetra Pak container UPC 8 42096-11234 8. Sold in 4 count Package wrap with UPC 842096122347. Shake Well. Best Chilled. Manufactured for: Aloha, Littleton, CO 80127

Quantity

53,818,025 Total Units

Reason

Findings and potential for Cronobacter sakazakii and Clostridium botulinum.

Recall initiation date

July 22, 2022

Report date

September 7, 2022

Classification date

Not published in this source record

Termination date

July 25, 2024

Distribution pattern

Nationwide

UPC, lot, and code information

UPC 842096122347; Lot Code 7312 / Best By Date 7/11/2023 EXPANDED 8-10-2022 Lot Code 0702 / Best By Date 05/05/2023. Lot Code 1221 / Best By Date 10/03/2022. Lot Code 2221 / Best By Date 10/04/2022. Lot Code 4821 / Best By Date 12/05/2022. Lot Code 5821 / Best By Date 12/06/2022. Lot Code 8811 / Best By Date 08/31/2022.

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Telephone

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 90667 with 10 other product entries in Public Health Trace.

Responsible company: Lyons Magnus, Inc

Other recalls from Lyons Magnus, Inc

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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