Skip to main content
CriticalFDAfda-F-1063-2019UNDECLARED ALLERGEN

Ottogi Snack Ramen 5PK, Cup 1lb 3.05oz x 8pk, 2.18oz x 6ea Item #21501281, 21502161 Manufactured by: Ottogi Ramyon Co. Ltd. Distribut...

⚠ Critical Alert — Stop Using Immediately

This product has been flagged with severe risks (undeclared allergen). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.

Units Affected
1,594,338
Recall Date
January 15, 2019
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1063-2019.

Undeclared allergen; egg.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1063-2019.

Recall terminated by FDA.

✅ What you should do

  1. Stop using the product if you own it.
  2. Check the model number, lot code, or sell-by date against the recall notice above.
  3. Contact Ottogi America Inc or the retailer where you bought it for a refund, replacement, or repair.
  4. For the most current official instructions, visit the FDA recall page.
  5. If you've been hurt by this product, report the incident to FDA.

Consumer Contact (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1063-2019.

Ottogi America Inc

FDA

About the U.S. Food and Drug Administration

The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.

Visit FDA.gov →

📣 Report a food, supplement, or cosmetic problem to the FDA

If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.

How to report to FDAFile a report at FDA

Ottogi America Inc Recall FAQ

Ottogi America Inc is the subject of a snacks & candy safety report: Ottogi Snack Ramen 5PK, Cup 1lb 3.05oz x 8pk, 2.18oz x 6ea Item #21501281, 21502161 Manufactured by: Ottogi Ramyon Co. Ltd. Distribut.... The notice was published on January 15, 2019 by the U.S. Food and Drug Administration (FDA). Approximately 1,594,338 units are potentially affected.