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CNC Noodle Corporation Recall: Undeclared wheat.

United States

OngoingClass II

Company
CNC Noodle Corporation
Product
Secondary Packaging: STEAM NOODLES INGREDIENTS: ENRICHED FLO…
Recall date
March 2, 2026
Source
FDA

Reason for recall

Undeclared wheat.

  1. - Recall initiated
  2. - Reported by source
Recalled products
Product description UPC Quantity Lot / code information
Secondary Packaging: STEAM NOODLES INGREDIENTS: ENRICHED FLOUR, WATER, STARCH, SALT, POTASSIUM, CARBONATE AND BENZOATE OF SODA ADDED AS PRESERVATIVEM F.D. & C. YELLOW COLOR #5 & #6 (TARTRAZINE) ARTIFICIAL COLORS) Primary Packaging: CHINA NOODLE CO. STEAM NOODLE NET WEIGHT 10 LBS. (4536 grams) PERISHABLE KEEP REFRIGERATED INGREDIENTS: ENRICHED WHEAT FLOUR (BLEACHED WHEAT FLOUR, NIACIN, IRON, ASCORBIC ACID, THIAMIN MONONITRATE, RIBOFLAVIN), WATER, SALT, SOYBEAN OIL, SODIUM BI-CARBONATE, 1/1000 BENZOATE OF SODIUM, DUSTED WITH CORN STARCH, ADDED AS A PRESERVATIVE, F.D. & C. YELLOW COLOR #5 AND #6 (TARTRAZINE) (ARTIFICIAL COLORS). ALLERGY INFORMATION: WHEAT Not published in this source record 427 cases (3-10 lb. bags/case) Lot code (Julian date): 047; 054; 056; 058 Item code: 1113

Distribution

  • U.S. Distribution: CA
  • NV. Foreign Distribution: None

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
H-0613-2026
Event ID
98522
Status
Ongoing
Classification
Class II
Company
CNC Noodle Corporation
Product description
Secondary Packaging: STEAM NOODLES INGREDIENTS: ENRICHED FLOUR, WATER, STARCH, SALT, POTASSIUM, CARBONATE AND BENZOATE OF SODA ADDED AS PRESERVATIVEM F.D. & C. YELLOW COLOR #5 & #6 (TARTRAZINE) ARTIFICIAL COLORS) Primary Packaging: CHINA NOODLE CO. STEAM NOODLE NET WEIGHT 10 LBS. (4536 grams) PERISHABLE KEEP REFRIGERATED INGREDIENTS: ENRICHED WHEAT FLOUR (BLEACHED WHEAT FLOUR, NIACIN, IRON, ASCORBIC ACID, THIAMIN MONONITRATE, RIBOFLAVIN), WATER, SALT, SOYBEAN OIL, SODIUM BI-CARBONATE, 1/1000 BENZOATE OF SODIUM, DUSTED WITH CORN STARCH, ADDED AS A PRESERVATIVE, F.D. & C. YELLOW COLOR #5 AND #6 (TARTRAZINE) (ARTIFICIAL COLORS). ALLERGY INFORMATION: WHEAT
Quantity
427 cases (3-10 lb. bags/case)
Reason
Undeclared wheat.
Recall initiation date
March 2, 2026
Report date
March 18, 2026
Classification date
Not published in this source record
Termination date
Not terminated as of this source record
Distribution pattern
U.S. Distribution: CA, NV. Foreign Distribution: None
UPC, lot, and code information
Lot code (Julian date): 047; 054; 056; 058 Item code: 1113
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Letter
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Other products recalled under this same event

This recall shares FDA event ID 98522 with 1 other product entry in Public Health Trace.

FDA Recall United States Ongoing 2026 recordClass II

CNC Noodle Corporation

Product
Secondary Packaging: ZHONG HUA CHAO MIAN NOODLE INGREDIENTS:…
Published
March 18, 2026
Distribution
U.S. Distribution: CA, NV. Foreign Distr…

View recall →

Responsible company: CNC Noodle Corporation

Other recalls from CNC Noodle Corporation

FDA Recall United States Ongoing 2026 recordClass II

CNC Noodle Corporation

Product
Secondary Packaging: ZHONG HUA CHAO MIAN NOODLE INGREDIENTS:…
Published
March 18, 2026
Distribution
U.S. Distribution: CA, NV. Foreign Distr…

View recall →

Distribution map

A map highlighting the states named in the source's distribution description.

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map
State Distributed
California 1
Nevada 1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Ongoing." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.