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Fresh Express Incorpated Recall: Fresh Express American had inadvertently inserted incorrect condiment kits in some bags.

United States

TerminatedClass I

Company
Fresh Express Incorpated
Product
Fresh Express American Salad, 11 oz., Product Code G264A12B,…
Recall date
September 29, 2016
Terminated
July 18, 2017
Source
FDA

Reason for recall

Fresh Express American had inadvertently inserted incorrect condiment kits in some bags.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Fresh Express American Salad, 11 oz., Product Code G264A12B, Use-By Date OCT 05 Not published in this source record 480 cases/6 bags (2880 bags) G264A12B

Distribution

  • AL
  • FL
  • GA
  • NC
  • SC & TN

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0146-2017
Event ID
75331
Status
Terminated
Classification
Class I
Company
Fresh Express Incorpated
Product description
Fresh Express American Salad, 11 oz., Product Code G264A12B, Use-By Date OCT 05
Quantity
480 cases/6 bags (2880 bags)
Reason
Fresh Express American had inadvertently inserted incorrect condiment kits in some bags.
Recall initiation date
September 29, 2016
Report date
October 26, 2016
Classification date
Not published in this source record
Termination date
July 18, 2017
Distribution pattern
AL, FL, GA, NC, SC & TN
UPC, lot, and code information
G264A12B
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: Fresh Express Incorpated

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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
Alabama 1
Florida 1
Georgia 1
North Carolina 1
South Carolina 1
Tennessee 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.

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.

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.