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Advanced Fresh Concepts Corp Recall: Product may be contaminated with listeria monocytogenes

United States

TerminatedClass I

Company
Advanced Fresh Concepts Corp
Product
AFC Edamame Soybeans in Pods, 8 oz , refrigerated, in cardbo…
Recall date
March 13, 2017
Terminated
May 1, 2017
Source
FDA

Reason for recall

Product may be contaminated with listeria monocytogenes

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
AFC Edamame Soybeans in Pods, 8 oz , refrigerated, in cardboard container. UPC 0-23012-00261-9 0-23012-00261-9 N/A UPC 0-23012-00261-9, dated between 01/03/2017 and 03/17/2017

Distribution

  • The products were packaged by AFC Franchisees and sold
  • under refrigeration
  • in 8.0 oz (227 g) packages and identified as Edamame  Soybeans in Pods. The packed Edamame was sold at designated retail sushi counters within grocery stores
  • cafeterias
  • and corporate dining centers in the following states: AL
  • AZ
  • CA
  • CO
  • CT
  • DC
  • FL
  • GA
  • IA
  • ID
  • IL
  • IN
  • KS
  • KY
  • LA
  • MA
  • ME
  • MI
  • MN
  • MS
  • NC
  • NH
  • NM
  • NY
  • OH
  • OR
  • PA
  • SC
  • TN
  • TX
  • VA
  • WA
  • and WY. The bulk product was distributed to franchisees between

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-1957-2017
Event ID
76771
Status
Terminated
Classification
Class I
Company
Advanced Fresh Concepts Corp
Product description
AFC Edamame Soybeans in Pods, 8 oz , refrigerated, in cardboard container. UPC 0-23012-00261-9
Quantity
N/A
Reason
Product may be contaminated with listeria monocytogenes
Recall initiation date
March 13, 2017
Report date
April 26, 2017
Classification date
Not published in this source record
Termination date
May 1, 2017
Distribution pattern
The products were packaged by AFC Franchisees and sold, under refrigeration, in 8.0 oz (227 g) packages and identified as Edamame  Soybeans in Pods. The packed Edamame was sold at designated retail sushi counters within grocery stores, cafeterias, and corporate dining centers in the following states: AL, AZ, CA, CO, CT, DC, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, ME, MI, MN, MS, NC, NH, NM, NY, OH, OR, PA, SC, TN, TX, VA, WA, and WY. The bulk product was distributed to franchisees between
UPC, lot, and code information
UPC 0-23012-00261-9; UPC 0-23012-00261-9, dated between 01/03/2017 and 03/17/2017
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
E-Mail
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Advanced Fresh Concepts Corp

Other recalls from Advanced Fresh Concepts Corp

FDA Recall United States Terminated Historical recordClass II

Advanced Fresh Concepts Corp

Product
Sushi Ebi Cooked Butterfly Tail-On Whiteleg Shrimp; Tray +0…
Published
April 8, 2020
Distribution
Multiple states

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
Alabama 1
Arizona 1
California 1
Colorado 1
Connecticut 1
District of Columbia 1
Florida 1
Georgia 1
Iowa 1
Idaho 1
Illinois 1
Indiana 1
Kansas 1
Kentucky 1
Louisiana 1
Massachusetts 1
Maine 1
Michigan 1
Minnesota 1
Mississippi 1
North Carolina 1
New Hampshire 1
New Mexico 1
New York 1
Ohio 1
Oregon 1
Pennsylvania 1
South Carolina 1
Tennessee 1
Texas 1
Virginia 1
Washington 1
Wyoming 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.