RecallHawk
Class II Recall

Item 81146 Ajinomoto Tai Pei Shrimp Fried Rice - Shrimp, vegetables & fried rice with oyster flavored sauce. Net wt. 48o

Ajinomoto Foods North America Inc.

Summary

The FDA issued a Class II for Item 81146 Ajinomoto Tai Pei Shrimp Fried Rice - Shrimp, vegetables & fried rice by Ajinomoto Foods North America Inc.. Reason: Foreign objects are glass varying in size from 1-3cm long and 2-4mm wide..

Details

Source

Food Recall

External ID

H-0597-2026

Action Date

2026-04-01

Status

Ongoing

Category

food

Product Description

Item 81146 Ajinomoto Tai Pei Shrimp Fried Rice - Shrimp, vegetables & fried rice with oyster flavored sauce. Net wt. 48oz or 3lbs. per box. Retail box UPC 070077811465. Product packaging is flexible bags in a master case or flexible bags in cartons in a master case. There are 4/48oz. boxes or 12lbs. per case. Case UPC 10070077811462. All products are intended to be stored frozen and fully cooked to 165F before eating.

Lot/Code Info: Best By Dates Range: 01/18/2027 to 3/10/2027 Best By Dates 1/18/2027 1/21/2027 2/16/2027 3/10/2027

Quantity Affected: 118,956 lbs. or 9,913 cases (12 lbs. per case)

Reason for Recall

Foreign objects are glass varying in size from 1-3cm long and 2-4mm wide.

Distribution

Distributed in AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NV, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, WA, WI, and WY.

Type: Voluntary: Firm initiated

Recall Initiated: 2026-03-03

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 64 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Ajinomoto Foods North America Inc. has 11 FDA actions in our database, including 11 recalls.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Ajinomoto Foods North America Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Ajinomoto Foods North America Inc. have FDA actions?

Ajinomoto Foods North America Inc. has 11 FDA actions in our database, including 11 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0597-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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