FDA recall record

Kraft Foods Group Low-Moisture Part-Skim Mozzarella String Cheese, sold under recall — FDA F-0401-2014

Some varieties of Kraft and Polly-O String Cheese and String Cheese Twist products may spoil before their "Best When Used By" code dates, leading to…

Class IIclassification
F-0401-2014official record ID
Dec 4, 2013report date

Recall record at a glance

Official recordF-0401-2014
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmKraft Foods Group
Report dateDec 4, 2013
Recall initiation dateOct 25, 2013
Quantity245,722 cases
LocationNorthfield, IL, United States

Official product description

Low-Moisture Part-Skim Mozzarella String Cheese, sold under Kraft brand or Polly-O brand and packaged with either 12, 16, 24, or 48 pieces of mozzarella cheese individually wrapped in plastic and sold in a plastic bag with a net weight respectively of 12 oz. (340g), 16 oz. (1 lb.) (453 g), 24 oz. (1 lb. 8 oz.) (680g), or 48 oz. (3 lb.) (1.36 kg.).

Why the product was recalled

Some varieties of Kraft and Polly-O String Cheese and String Cheese Twist products may spoil before their "Best When Used By" code dates, leading to product discoloration. The affected products all have code dates from October 25, 2013 through February 11, 2014.

Distribution information

US: Nationwide (AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, WA, WI, WV, WY) + Guam + 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

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.

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