RecallHawk
Class I Recall

PROUCT WAS NOT DISTRIBUTED IN US. The Original Oatly! Oat Drink Deluxe 330ml. UPC 7 394376 619021 18 count case UPC

Lyons Magnus, Inc

Summary

The FDA issued a Class I for PROUCT WAS NOT DISTRIBUTED IN US. The Original Oatly! Oat Drink Deluxe 330ml. by Lyons Magnus, Inc. Reason: Findings and potential for Cronobacter sakazakii and Clostridium botulinum..

Details

Source

Food Recall

External ID

F-1676-2022

Action Date

2022-09-07

Status

Terminated

Category

food

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.

Lot/Code Info: 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

Quantity Affected: 53,818,025 total units

Reason for Recall

Findings and potential for Cronobacter sakazakii and Clostridium botulinum.

Distribution

Nationwide

Type: Voluntary: Firm initiated

Recall Initiated: 2022-07-22

Company

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 111 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Lyons Magnus, Inc has 78 FDA actions in our database, including 78 recalls.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Lyons Magnus, Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Lyons Magnus, Inc have FDA actions?

Lyons Magnus, Inc has 78 FDA actions in our database, including 78 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1676-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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