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Market of Choice Inc Recall: Sezam Kale Salad kits, 6.43 lbs, are recalled due to undeclared egg. The wrong dressing packet was added to the Sezam Kale Salad kit and the dressing contains undeclared egg.

United States

TerminatedClass I

Company
Market of Choice Inc
Product
Sezam Kale Salad ingredient kits, net wt. 6.43 pound. Ingre…
Recall date
February 20, 2018
Terminated
March 5, 2018
Source
FDA

Reason for recall

Sezam Kale Salad kits, 6.43 lbs, are recalled due to undeclared egg. The wrong dressing packet was added to the Sezam Kale Salad kit and the dressing contains undeclared egg.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Sezam Kale Salad ingredient kits, net wt. 6.43 pound. Ingredients are packaged individually and then placed in one large bag. The ingredients from the kit was mixed and sold in deli cases at retail stores. The product sold in deli cases has the UPC 2 11565 20216 1. Not published in this source record 16 kits (6.43 lbs. per kit) Production code 02-14-18 (sell by date of 02-21-18) Production code 02-15-18 (sell by date of 02-22-18)

Distribution

  • distributed in OR

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0878-2018
Event ID
79300
Status
Terminated
Classification
Class I
Company
Market of Choice Inc
Product description
Sezam Kale Salad ingredient kits, net wt. 6.43 pound. Ingredients are packaged individually and then placed in one large bag. The ingredients from the kit was mixed and sold in deli cases at retail stores. The product sold in deli cases has the UPC 2 11565 20216 1.
Quantity
16 kits (6.43 lbs. per kit)
Reason
Sezam Kale Salad kits, 6.43 lbs, are recalled due to undeclared egg. The wrong dressing packet was added to the Sezam Kale Salad kit and the dressing contains undeclared egg.
Recall initiation date
February 20, 2018
Report date
March 7, 2018
Classification date
Not published in this source record
Termination date
March 5, 2018
Distribution pattern
distributed in OR
UPC, lot, and code information
Production code 02-14-18 (sell by date of 02-21-18) Production code 02-15-18 (sell by date of 02-22-18)
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

Responsible company: Market of Choice Inc

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Published
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Distribution
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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
Oregon 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 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.

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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?

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