Ottogi Jin Ramen Mild Recalled for Undeclared Egg Allergen
Ottogi America Inc. is recalling Ottogi Jin Ramen Mild 5-packs due to an undeclared egg allergen. The product was distributed in five U.S. states and Canada.
What this means for you
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The FDA classified this recall as Class I, which indicates a reasonable probability that the use of, or exposure to, the violative product will cause serious adverse health consequences or death. Per the rubric, FDA Class I recalls must be scored at least 4.
Plain-English summary
Ottogi America Inc. is recalling specific packages of Ottogi Jin Ramen Mild. The recall is being conducted because the product contains an undeclared allergen: egg. The affected product is the 1lb 5.16oz (600g) 5-pack, manufactured by Ottogi Ramyon Co. Ltd. and distributed by Ottogi America, Inc. in Gardena, California.
The recall covers products with a 'BEST BEFORE' date of AUG 19 2019. The product was distributed in the United States to California, New Jersey, Hawaii, Texas, and Illinois. It was also distributed to Canada.
Consumers with this product should stop using it and check with the recalling firm for instructions on how to dispose of or return the product. The FDA classifies this recall as Class I, which is the most serious type of recall.
The recalled product
- Product
- Ottogi Jin Ramen Mild NET WT. 1lb 5.16oz, 600g (120gx5) 5PK Manufactured by: Ottogi Ramyon Co. Ltd. Distributed by: Ottogi America, Inc. 1650 W. El Segundo Bl. Gardena, CA 90249
- Manufacturer
- Ottogi America Inc
- Category
- Food — Ramen / Noodles
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)
- BEST BEFORE AUG 19 2019
Distribution
Part of a larger recall action
This product is one of 2 recalled by Ottogi America 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 2 products in this recall →Related recalls
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