The Original Oatly! Oat Drink Chocolate 11 fl oz (330ml). UPC 1 90646-63015 7. 18 count case UPC 20190646630151. Dis
Summary
The FDA issued a Class I for The Original Oatly! Oat Drink Chocolate 11 fl oz (330ml). UPC 1 90646-63015 7. by Lyons Magnus, Inc. Reason: Findings and potential for Cronobacter sakazakii and Clostridium botulinum..
Details
Source
Food Recall
External ID
F-1674-2022
Action Date
2022-09-07
Status
Terminated
Category
food
Product Description
The Original Oatly! Oat Drink Chocolate 11 fl oz (330ml). UPC 1 90646-63015 7. 18 count case UPC 20190646630151. Distributed by Oatly Inc., 220 E 42ndSt., Ste. 409A, New York, NY 10017.
Lot/Code Info: EXPANDED 8-10-2022 Lot Code 0502 / Best By Date 19Feb2023 LM Lot Code 2202 / Best By Date 22Jan2023 LM Lot Code 5531 / Best By Date 21Dec2022 LM Lot Code 6231 / Best By Date 22Nov2022 LM Lot Code 6531 / Best By Date 22Dec2022 LM Lot Code 7231 / Best By Date 23Nov2022 LM Lot Code 7531 / Best By Date 23Dec2022 LM Lot Code 8402 / Best By Date 17Feb2023 LM Lot Code 8802 / Best By Date 29Mar2023 LM Lot Code 9402 / Best By Date 18Feb2023 LM Lot Code 9802 / Best By Date 30Mar2023 LM
Quantity Affected: 53,818,250 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
Fresno, CA
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-1674-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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