Recall record at a glance
| Official record | F-1057-2022 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Ramen Hero |
| Report date | May 18, 2022 |
| Recall initiation date | Apr 12, 2022 |
| Quantity | 1416 units |
| Location | Berkeley, CA, United States |
Official product description
Ramen Hero - Vegan Shoyu ramen (Hippie Van) Ramen noodles in a soy sauce infused vegan broth with a vegan meat ragu, roasted tomato, bell pepper and zucchini blend, and seaweed. Kits are in a frosted meal kit stand up pouch. Net Wt. 20.05 oz. (1.25 lb.) 568 g UPC: 60003 Contains: Soy, Treenut (coconut) Wheat, Sulfites. Distributed by: Ramen Hero, 2001 Addison St. Suite 300, Berkeley, CA 94704
Why the product was recalled
Affected lots of Vegan Shoyu Ramen meal kits used egg noodles which contain egg. The allergen of egg is not listed on the product label.
Distribution information
E-commerce sales and to 3 retail locations in CA and NY
How to read the classification
FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Telephone.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.
FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.