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Ahold Usa Recall: Ahold U.S.A., Inc. was notified by the Virginia Department of Agriculture that one of three retail samples of Whole Kernel Corn, 16 oz. tested positive for Listeria Monocytogenes on 11/13/2017. The firm has decided to initiate a recall of the product . - F-0421-2018

United States

TerminatedClass II

Company
Ahold Usa
Product
Ahold-Own Brands Whole Kernel Sweet Corn, 16 oz. Plastic Ba…
Recall date
November 14, 2017
Terminated
July 23, 2021
Source
FDA

Reason for recall

Ahold U.S.A., Inc. was notified by the Virginia Department of Agriculture that one of three retail samples of Whole Kernel Corn, 16 oz. tested positive for Listeria Monocytogenes on 11/13/2017. The firm has decided to initiate a recall of the product .

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Ahold-Own Brands Whole Kernel Sweet Corn, 16 oz. Plastic Bag : Stop & Shop Brand Frozen Whole Kernel Sweet Corn, 16 oz. GIANT/MARTIN S Brand Frozen Whole Kernel Sweet Corn, 16 oz. Giant Brand Frozen Whole Kernel Sweet Corn, 16 oz. Not published in this source record 3793 Cases Best by Oct 2019 B7 276 2. Produced in Canada Stop & Shop Brand Frozen Whole Kernel Sweet Corn, 16 oz., UPC 68826700676 GIANT/MARTIN S Brand Frozen Whole Kernel Sweet Corn, 16 oz., UPC 68826700676 Giant Brand Frozen Whole Kernel Sweet Corn, 16 oz., UPC 68826700676

Distribution

  • The firm distributed product to the following Direct Accounts: 1). C&S Aberdeen
  • MD 2). C&S Giant
  • York
  • PA 3). C&S Westfield
  • MA 4). C&S Giant
  • York
  • PA 5). C&S Westfield
  • MA Please see attached excel spread sheet for detail list of Retail Stores.

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0421-2018
Event ID
78576
Status
Terminated
Classification
Class II
Company
Ahold Usa
Product description
Ahold-Own Brands Whole Kernel Sweet Corn, 16 oz. Plastic Bag : Stop & Shop Brand Frozen Whole Kernel Sweet Corn, 16 oz. GIANT/MARTIN S Brand Frozen Whole Kernel Sweet Corn, 16 oz. Giant Brand Frozen Whole Kernel Sweet Corn, 16 oz.
Quantity
3793 Cases
Reason
Ahold U.S.A., Inc. was notified by the Virginia Department of Agriculture that one of three retail samples of Whole Kernel Corn, 16 oz. tested positive for Listeria Monocytogenes on 11/13/2017. The firm has decided to initiate a recall of the product .
Recall initiation date
November 14, 2017
Report date
December 6, 2017
Classification date
Not published in this source record
Termination date
July 23, 2021
Distribution pattern
The firm distributed product to the following Direct Accounts: 1). C&S Aberdeen, MD 2). C&S Giant, York, PA 3). C&S Westfield, MA 4). C&S Giant, York, PA 5). C&S Westfield, MA Please see attached excel spread sheet for detail list of Retail Stores.
UPC, lot, and code information
Best by Oct 2019 B7 276 2. Produced in Canada Stop & Shop Brand Frozen Whole Kernel Sweet Corn, 16 oz., UPC 68826700676 GIANT/MARTIN S Brand Frozen Whole Kernel Sweet Corn, 16 oz., UPC 68826700676 Giant Brand Frozen Whole Kernel Sweet Corn, 16 oz., UPC 68826700676
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: Ahold Usa

Other recalls from Ahold Usa

FDA Recall United States TerminatedTerminated: July 23, 2021Historical recordClass II

Ahold Usa

Product
Broccoli cuts, All Natural, No Preservatives, Net Wt 16 OZ;…
Published
June 13, 2018
Distribution
CT, DC, MD, MA, NJ, NY PA, RI, VA and WV

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
Maryland 1
Pennsylvania 1
Massachusetts 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.

This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.

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Technical source data

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Retrieved by Public Health Trace:

Frequently asked questions

What does a Class II mean?

FDA classifies this recall as Class II. See how to read an FDA recall record (linked above) for what each classification level means.

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 responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.

Official guidance and record verification

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How to interpret this historical record

This record is preserved as published by FDA, as of July 23, 2021.

Status as reported: Terminated.

This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.

View the official FDA source

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.

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