FDA recall record

Ahold Usa 16 oz recall — FDA F-0421-2018

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…

Class IIclassification
F-0421-2018official record ID
Dec 6, 2017report date

Recall record at a glance

Official recordF-0421-2018
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmAhold Usa
Report dateDec 6, 2017
Recall initiation dateNov 14, 2017
Quantity3793 Cases
LocationQuincy, MA, United States

Official 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.

Why the product was recalled

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 .

Distribution information

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.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

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