FDA recall record

Kraft Foods Group 7.25oz.,packaged in blue and yellow cardboard box recall — FDA F-1955-2015

This voluntary recall has been initiated because Kraft Macaroni & Cheese Boxed Dinners may contain metal pieces.

Class IIclassification
F-1955-2015official record ID
Apr 22, 2015report date

Recall record at a glance

Official recordF-1955-2015
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmKraft Foods Group Inc.
Report dateApr 22, 2015
Recall initiation dateMar 17, 2015
Quantity242,000 cases
LocationChampaign, IL, United States

Official product description

Kraft Macaroni & Cheese Boxed Dinner Original Flavor, 7.25oz.,packaged in blue and yellow cardboard box. There are four different package types affected by this recall: 1) single 7.25 oz boxes, 3-pack box of 7.25 oz boxes, 4-pack shrink wrap of 7.25 oz boxes, and 5-pack shrink wrap of 7.25 oz boxes.

Why the product was recalled

This voluntary recall has been initiated because Kraft Macaroni & Cheese Boxed Dinners may contain metal pieces.

Distribution information

*** US: Nationwide ( AL, AR, AZ, CA, CT, FL, GA, HI, IL, KS, KY, MA, MD, ME, MI, MN, MO, MS, NC, ND, NJ, NM, NV, NY, OH, OK, OR, PA, PR, SC, TN, VA, VI, WA, WI) *** FOREIGN: Bahamas, El Salvador, Guyana, Saint Kitts and Nevis, Panama

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

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.