CLASS I Food recall · Reported 7 Sep 2022 · FDA Enforcement Report
Intelligentsia, Oat Latte recalled by Lyons Magnus
Lyons Magnus is recalling Intelligentsia, Oat Latte, distributed nationwide in the US. The recall was initiated on 22 Jul 2022 and the FDA has classified it as Class I.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-1608-2022
- FDA event ID
- 90667
- Recalling firm
- Lyons Magnus, Fresno, CA
- Brand
- Intelligentsia
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 22 Jul 2022
- FDA classified
- 30 Aug 2022
- Reported
- 7 Sep 2022
- Type
- Voluntary: Firm initiated
- Customers notified by
- Telephone
- Reason category
- Botulism
- Product category
- Milk
Timeline
| 22 Jul 2022 | Recall initiated by company | |
| 30 Aug 2022 | Classified by FDA | +39 days |
| 7 Sep 2022 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Findings and potential for Cronobacter sakazakii and Clostridium botulinum.
Product as listed by the FDA
Intelligentsia, Oat Latte. Cold Coffee + Oat Milk. Net 10.9 fl oz (325 mL) Tetra Pak container UPC 8 00222-00097 6. Refrigerate after opening. Produced for: Intelligentsia Coffee, Inc., Aloha, Chicago, IL 60612.
Where it was distributed
Nationwide
Questions about this recall
Is Intelligentsia, Oat Latte recalled?
Yes. Lyons Magnus recalled Intelligentsia, Oat Latte on 22 Jul 2022. The recall is Class I and its status is Terminated. Recall number F-1608-2022.
Why was it recalled?
Findings and potential for Cronobacter sakazakii and Clostridium botulinum.
Which lots are affected?
Lot Code 7112 / Best By Date 01/04/2023 Lot Code 8112 / Best By Date 01/05/2023
Where was it sold?
Nationwide
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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