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-1676-2022

Event ID

90667

Status

Terminated

Classification

Class I

Company

Lyons Magnus, Inc

Product description

PROUCT WAS NOT DISTRIBUTED IN US. The Original Oatly! Oat Drink Deluxe 330ml. UPC 7 394376 619021 18 count case UPC 27394376619025. Shake well before drinking. Produced in the USA. Oatly AB, Stora Varvsgatan 6a, SE-211 19 Malmo.

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 27394376619025; EXPANDED 8-10-2022 Lot Code 1102 / Best By Date 2023.01.11 Lot Code 2031 / Best By Date 2022.10.29 Lot Code 3031 / Best By Date 2022.10.30 Lot Code 4031 / Best By Date 2022.10.31 Lot Code 5031 / Best By Date 2022.11.01 Lot Code 5231 / Best By Date 2022.11.21 Lot Code 6231 / Best By Date 2022.11.21 Lot Code 7402 / Best By Date 2023.02.16 Lot Code 7521 / Best By Date 2022.09.14 Lot Code 7531 / Best By Date 2022.12.23 Lot Code 8521 / Best By Date 2022.09.15 Lot Code 8531 / Best By Date 2022.12.24

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 9 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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