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Mai Cuisine LLC Recall: Product is recalled due to undeclared egg.

United States

TerminatedClass I

Company
Mai Cuisine LLC
Product
Spicy Shrimp Tempura Crunch Roll, Mai brand, packed in conta…
Recall date
June 16, 2019
Terminated
July 19, 2019
Source
FDA

Reason for recall

Product is recalled due to undeclared egg.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Spicy Shrimp Tempura Crunch Roll, Mai brand, packed in container with clear plastic lid,net wt. 9.1 oz., UPC 8 12824 01526 5. The label is read in parts: "***MAI SPICY SHRIMP TEMPURA CRUNCH ROLL ***KEEP REFRIGERATED***Allergen: SOY, WHEAT, SHELLFISH***"dist by Mai Sushi 2 Penn Center, Suite 725, 1500 JFK Blvd Philadelphia, PA*** Not published in this source record 35 pkg. crunch roll Hand-Crafted Date of 6/15/2019 and Best by Date of 6/17/2019.

Distribution

  • distributed in Oregon

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-1530-2019
Event ID
83157
Status
Terminated
Classification
Class I
Company
Mai Cuisine LLC
Product description
Spicy Shrimp Tempura Crunch Roll, Mai brand, packed in container with clear plastic lid,net wt. 9.1 oz., UPC 8 12824 01526 5. The label is read in parts: "***MAI SPICY SHRIMP TEMPURA CRUNCH ROLL ***KEEP REFRIGERATED***Allergen: SOY, WHEAT, SHELLFISH***"dist by Mai Sushi 2 Penn Center, Suite 725, 1500 JFK Blvd Philadelphia, PA***
Quantity
35 pkg. crunch roll
Reason
Product is recalled due to undeclared egg.
Recall initiation date
June 16, 2019
Report date
July 3, 2019
Classification date
Not published in this source record
Termination date
July 19, 2019
Distribution pattern
distributed in Oregon
UPC, lot, and code information
Hand-Crafted Date of 6/15/2019 and Best by Date of 6/17/2019.
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
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 83157 with 1 other product entry in Public Health Trace.

FDA Recall United States Terminated Historical recordClass I

Mai Cuisine LLC

Product
Spicy Shrimp Tempura Roll, Mai brand, packed in container wi…
Published
July 3, 2019
Distribution
distributed in Oregon

View recall →

Responsible company: Mai Cuisine LLC

Other recalls from Mai Cuisine LLC

FDA Recall United States Terminated Historical recordClass I

Mai Cuisine LLC

Product
Spicy Shrimp Tempura Roll, Mai brand, packed in container wi…
Published
July 3, 2019
Distribution
distributed in Oregon

View recall →

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 I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Terminated." 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.

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