Stumptown Cold Brew Coffee Recalled for Cronobacter and Botulism Risk
Stumptown Cold Brew Coffee with Oatmilk Original is recalled nationwide due to potential contamination with Cronobacter sakazakii and Clostridium botulinum. This FDA Class I recall affects approximately 53.8 million units.
What this means for you
Highest-severity recall. Risk of serious injury or death is documented or strongly suspected. Stop using the product now and follow the agency's instructions.
Our severity reasoning: FDA Class I classification meets the Critical severity criterion. Class I is the FDA's most serious recall classification, indicating a reasonable probability that use of the product will cause serious adverse health consequences.
Plain-English summary
Lyons Magnus, Inc., the manufacturer of Stumptown Cold Brew Coffee with Oatmilk Original (11 fl oz bottles, UPC 855186006878), has issued a nationwide Class I recall due to findings and potential presence of Cronobacter sakazakii and Clostridium botulinum.
The affected lot codes are: Lot Code 2312 (Best By Date 12/08/2022), Lot Code 3312 (Best By Date 12/09/2022), and Lot Code 9202 (Best By Date 08/27/2022). Approximately 53.8 million units have been distributed nationwide.
Consumers should not consume this product. Check refrigerators and pantries for bottles matching the affected lot codes and best-by dates. Return the product to the retailer or dispose of it safely. If you have consumed this product and experience fever, abdominal pain, or symptoms of botulism such as muscle weakness or difficulty swallowing, seek medical attention immediately and inform your healthcare provider of potential exposure.
The recalled product
- Product
- 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
- Manufacturer
- Lyons Magnus, Inc
- Affected units
- 53,818,025
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Lot Code 2312 / Best By Date 12/08/2022
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 77 recalled by Lyons Magnus, Inc under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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