FDA recall record

The Dannon Company, Inc - Discovery & Innovation Dannon Activia LIGHT Nonfat Yogurt Peach recall — FDA F-1240-2013

The recalled products may potentially contain metal fragment(s) from a faulty manufacturing part.

Class IIclassification
F-1240-2013official record ID
Mar 27, 2013report date

Recall record at a glance

Official recordF-1240-2013
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmThe Dannon Company, Inc - Discovery & Innovation Center
Report dateMar 27, 2013
Recall initiation dateOct 23, 2012
Quantity2,430 cases / 6 / 4x4oz cups
LocationWhite Plains, NY, United States

Official product description

Dannon Activia LIGHT Nonfat Yogurt Peach Flavor 4x4oz cups INGREDIENTS: CULTURED GRADE A NONFAT MILK, WATER, PEACHES ***DISTRIBUTED BY: THE DANNON COMPANY, INC. WHITE PLAINS, NY 10603 UPC 36632 02633 Expiration code of DEC 04 2012 MZ

Why the product was recalled

The recalled products may potentially contain metal fragment(s) from a faulty manufacturing part.

Distribution information

The product was distributed nationwide including the states of: FL, GA, IL, IN, KY, MD, ME, MI, NC, NY, OH, PA, SC, VA, WI.

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

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.