FDA recall record

Mondelez Global Case UPC: 144000031944 Carton: Nabisco belVita Chocolate Net recall — FDA F-1068-2013

belVita breakfast biscuit may contain fragments of flexible metal mesh caused by a faulty screen at a third-party flour supplier.

Class IIclassification
F-1068-2013official record ID
Mar 20, 2013report date

Recall record at a glance

Official recordF-1068-2013
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmMondelez Global LLC
Report dateMar 20, 2013
Recall initiation dateFeb 21, 2013
Quantity460,917 cases (6 boxes in each case with 5 pouches that contain 4 cookies)
LocationEast Hanover, NJ, United States

Official product description

Case UPC: 144000031944 Carton: Nabisco belVita Chocolate Variety Net Wt. 8.8 oz UPC 0 44000 03194 7 Distributed by Kraft Foods Global, Inc. Northfield, IL 60093-2753 USA Inner Pouch: Nabisco belVita Chocolate Variety Net Wt. 1.76 oz UPC 0 44000 03192 3 Distributed by Kraft Foods Global, Inc. Northfield, IL 60093-2753 USA 14.08 oz Please note there are mixed shippers, shipper labels are not available: Mixed belVita Shipper UPC 0044000032784 which contains a 14.08 oz 2 pc product- waiting for label for this size. 9618 cases distributed.

Why the product was recalled

belVita breakfast biscuit may contain fragments of flexible metal mesh caused by a faulty screen at a third-party flour supplier.

Distribution information

Nationwide and Puerto Rico

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: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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