FDA recall record

CJ Foods Inc., A Division of CJ Annie Chun's Japanese Style Teriyaki Noodle Bowl with Cooked recall — FDA F-0757-2020

Pad Thai Noodle Bowl which contains peanuts was packaged with the sleeve for Teriyaki Noodle Bowl leaving undeclared peanuts on the product label.

Class IIclassification
F-0757-2020official record ID
Mar 4, 2020report date

Recall record at a glance

Official recordF-0757-2020
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmCJ Foods Inc., A Division of CJ America
Report dateMar 4, 2020
Recall initiation dateFeb 14, 2020
Quantity33,900 cases ( 6 bowls per case)
LocationLa Palma, CA, United States

Official product description

Annie Chun's Japanese Style Teriyaki Noodle Bowl with Cooked Hokkien Noodles - Sweet & Tangy sauce with Bok choy and carrots. Noodles are in Opaque White Plastic bowl with paper sleeves. Net Wt. 7.8 oz. (221g) UPC: 7-65667-10387-6 Add 1 1/4 water and microwave on high for 90 seconds on high. Distributed by: CJ Foods America, Fullerton, CA

Why the product was recalled

Pad Thai Noodle Bowl which contains peanuts was packaged with the sleeve for Teriyaki Noodle Bowl leaving undeclared peanuts on the product label.

Distribution information

WA, RI, CA, FL, TN, PA, MN, IL, WI, and IA

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Press Release.

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.