FDA recall record

Hmshost Woodstock Cape Cod Cranberry Mix, 25lbs recall — FDA F-2153-2016

Woodstock Farms informed HMSHost of their recall. HMSHost purchase bulk snacks from Woodstock Farms , has discovered during their routine testing that the…

Class Iclassification
F-2153-2016official record ID
Sep 28, 2016report date

Recall record at a glance

Official recordF-2153-2016
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmHmshost
Report dateSep 28, 2016
Recall initiation dateMay 9, 2016
QuantityTotal of 1,275 pounds
LocationBethesda, MD, United States

Official product description

Woodstock Cape Cod Cranberry Mix, 25lbs. Item #250575 The product also goes by the following trades names: 1). 1897 Cape Cod Cranberry Mix 7oz 2). Ciao Cape Cod Cranberry Mix 7oz 3). Farmers Market Cape Cod Cranberry Mix 7oz 4). Grounded In Cape Cod Cranberry Mix 7oz 5). La Tapenade Cape Cod Cranberry Mix 7oz 6). Marche Cape Cod Cranberry Mix 7oz 7). MKT Cape Cod Cranberry Mix 7oz 8). Pronto Cape Cod Cranberry Mix 7oz 9). PZA Cape Cod Cranberry Mix 7oz 10). The Local Cape Cod Cranberry Mix 7oz 11). Urban Market Cape Cod Cranberry Mix 7oz 12) Fresh Attraction Cape Cod Cranberry Mix 7oz

Why the product was recalled

Woodstock Farms informed HMSHost of their recall. HMSHost purchase bulk snacks from Woodstock Farms , has discovered during their routine testing that the walnuts used in the recalled items/products may have the presence of Listeria Monocytogenes. HMSHost repackaged the bulk snack under several private label brands to sell to the consumer. HMSHost is initiating a precautionary voluntary recall.

Distribution information

HMSHost received a total of 1,275 pounds of product under the lot codes that are recalled which were distributed to 34 customers in total. Distribution is only for US and to HMSHost Airports & Travel Plazas Concepts/Stores. No Foreign Country was affected.

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Telephone.

What to do next

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About this record

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