Stumptown Cold Brew Coffee with Oatmilk Original. Made with Oatly! Low Sugar. 11 Fl Oz. 325 ML. UPC 8 55186-00687
Summary
The FDA issued a Class I for Stumptown Cold Brew Coffee with Oatmilk Original. Made with Oatly! Low Sugar. by Lyons Magnus, Inc. Reason: Findings and potential for Cronobacter sakazakii and Clostridium botulinum..
Details
Source
Food Recall
External ID
F-1644-2022
Action Date
2022-09-07
Status
Terminated
Category
food
Product Description
Stumptown Cold Brew Coffee with Oatmilk Original. Made with Oatly! Low Sugar. 11 Fl Oz. 325 ML. UPC 8 55186-00687 8. Sold in 12-count case UPC 108551860006844. Manufactured for Stumptown Coffee Roasters, 100 SE Salmon St. Portland, OR 97214
Lot/Code Info: Lot Code 2312 / Best By Date 12/08/2022; Lot Code 3312 / Best By Date 12/09/2022. EXPANDED 8-10-2022 Lot Code 9202 / Best By Date 08/27/2022.
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
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-1644-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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