Cold Coffee Recalled Nationwide for Bacterial Contamination Risk
Intelligentsia Cold Coffee in 10.9 oz containers is recalled nationwide due to potential Cronobacter sakazakii and Clostridium botulinum contamination. Consumers should not consume the product.
The agency’s classification
FDA (Food): Class I
Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 4/5 (Severe).
The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: FDA Class I classification for bacterial pathogens (Cronobacter sakazakii and Clostridium botulinum) mandates minimum severity score of 4. No illnesses or injuries are reported in the source text.
Plain-English summary
Intelligentsia Cold Coffee, 10.9 fl oz Tetra Pak containers, is recalled nationwide. The product (Lot Code 9212, Best By Date 12/07/2022) was produced for Intelligentsia Coffee, Inc., located in Chicago, Illinois, by Lyons Magnus, Inc.
The recall was issued due to findings and potential for Cronobacter sakazakii and Clostridium botulinum contamination. These bacterial pathogens can cause serious illness.
Approximately 53,818,025 units were distributed nationwide. All consumers who may have purchased this product are potentially affected.
Consumers should not consume this product. Anyone who has consumed the product and experiences symptoms should contact their healthcare provider.
The recalled product
- Product
- Intelligentsia, Cold Coffee. Net 10.9 fl oz (325 mL) Tetra Pak container UPC 8 00222-00096 9. Shake Best enjoyed cold. Refrigerate after opening. Produced for: Intelligentsia Coffee, Inc., Aloha, Chicago, IL 60612.
- 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 9212 / Best By Date 12/07/2022
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.
See all 77 products in this recall →Related recalls
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