J-Basket Brand Napa Kimchi
Reason High levels of Yeast growth and film on top of jarred Kimchi product.
J-Basket Premium Korean Seaweed Snack recall
Recalled by J F C International Inc · Commerce, CA, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Wasabi Flavor Seaweed snack is incorrectly packaged in Original Seaweed Flavor package which does not declare FD&C Yellow 5 and FD&C Blue No 1.
A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.
What was recalled
J-Basket Premium Korean Seaweed Snack - Wasabi flavor on outer wrap for 3 inner packages Inner packages labeled J-Basket Premium Seaweed Snack - Original. Net Wt 0.52 oz. (15g) 3-0.17 oz. (5g) packs Distributed by JFC International Inc., Los Angeles, CA 90040 Wasabi outer package UPC 0 11152 29507 7 Ingredients: Wasabi: Seaweed, corn oil, sesame oil, wasabi powder (mustard {Ally Isothiocyante, Maltodextrin, arabic gum, palm oil, rosemary oleoresini}, dextrin, wasabi, FD&C Yellow #5, FD&C Blue No 1. Ingredients Original: Seaweed, Corn oil, Sesame oil, Salt.
Quantity: 451 boxes
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Best Before: 01.03.2022 / 01.10.2022, JFC Item#29507
Where it was sold
Arkansas Arizona California Iowa Illinois Kentucky Louisiana Michigan Missouri Nebraska Ohio Texas Washington Wisconsin
FDA's distribution note: CA, WA, AZ, TX, LA, AR, KY, NE, WI, IL, MO, IA, OH, MI.
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- J F C International Inc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Apr 8, 2021
- In FDA report of
- Apr 21, 2021
- Terminated
- May 24, 2021
- FDA recall number
- F-0429-2021 · event 87706
- Official record
- FDA enforcement report search
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