FDA recall record

Marathon Ventures Macadamia Diced Nuts packaged under the following brands: 1) recall — FDA F-1244-2016

Product potentially contaminated with Salmonella. Routine, random product sampling by FDA revealed the presence of Salmonella in a retail package of…

Class Iclassification
F-1244-2016official record ID
May 4, 2016report date

Recall record at a glance

Official recordF-1244-2016
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmMarathon Ventures Inc.
Report dateMay 4, 2016
Recall initiation dateFeb 23, 2016
Quantity5890 lbs.
LocationBellevue, NE, United States

Official product description

Macadamia Diced Nuts packaged under the following brands: 1) Shurfine, Item no. 86635, 5 OZ (142 g) plastic bags, packed 12 bags per case, UPC 0 15400 86635 4. Distributed by Western Family Foods, Inc., Portland OR. 2) Western Family, 5 OZ (142 g) plastic bags, packed 12 per case, UPC 0 15400 16635 5. Distributed by Western Family Foods, Inc., Portland, OR. 3) HyVee, 2 OZ (57 g) plastic bags, packed 12 per case, UPC 0 75450 13287 8. Distributed by HyVee, Inc., West Des Moines, IA. 4) Market Pantry, 2.25 OZ (64 g) plastic bags, packed 12 bags per case, UPC 0 85239 52108 3. Distributed by Target Corp., Minneapolis, MN. 5) Pear's Gourmet, 16 OZ (454 g) plastic bags, UPC 0 75049 42186 4. Pear's Gourmet, Bellevue, NE 68005. 6) CWD, 5 LBS. (2.27 kg) per 1-count case, UPC 06509. Packed for and distributed by Cash-Wa Distributing Co. Kearney, North Platte, Sidney, NE. and 7) Nutpro C.C. Macadamia Nuts Style #5, 25 LBS., bulk case item no. N0609. The responsible firm is Nutpro South Africa.

Why the product was recalled

Product potentially contaminated with Salmonella. Routine, random product sampling by FDA revealed the presence of Salmonella in a retail package of macadamia nuts packaged by the recalling firm.

Distribution information

Product was distributed to CA, CO, GA, IA, IN, MN, MO, NC, NE, OR, SC, TX, UT, VA, and WI. There was no military/government/foreign distribution.

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Press Release.

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.