FDA recall record

Inventure Foods RADER FARMS Fresh Start Sunrise Refresh Fusion, Walmart Item recall — FDA F-2088-2015

RADER FARMS Fresh Start Sunrise Refresh Fusion is recalled due to potential for contamination with Listeria monocytogenes.

Class IIclassification
F-2088-2015official record ID
May 6, 2015report date

Recall record at a glance

Official recordF-2088-2015
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmInventure Foods
Report dateMay 6, 2015
Recall initiation dateJan 17, 2015
Quantity4401 cases (4/35 oz. packages per case)
LocationPhoenix, AZ, United States

Official product description

RADER FARMS Fresh Start Sunrise Refresh Fusion, Walmart Item no. 552888782, Net wt. 35 oz. The UPC is 8 84038 85154 0

Why the product was recalled

RADER FARMS Fresh Start Sunrise Refresh Fusion is recalled due to potential for contamination with Listeria monocytogenes.

Distribution information

Fresh Start Smoothie Blend, 3 lbs. package size, is distributed in Alaska, Arizona, California, Colorado, Idaho, Montana, Nevada, New Mexico, Oregon, Utah, Washington, and in Alberta, British Columbia, Manitoba, and Saskatchewan of Canada. The Fresh Start Sunrise Refresh and Fresh Start Daily Power, 35-ounce package size, is distributed Alaska, Arizona, California, Colorado, Idaho, Montana, Nevada, New Mexico, Oregon, Texas, Utah, Washington, and Wyoming.

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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