CLASS II Food recall · Reported 6 May 2015 · FDA Enforcement Report

Rader Farms¿ Fresh Start Sunrise Refresh Fusion, Walmart recalled

Inventure Foods is recalling Rader Farms¿ Fresh Start Sunrise Refresh Fusion, Walmart, distributed in 13 states. The recall was initiated on 17 Jan 2015 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesBEST BY DATES: 6/30/2016; 2/14/2016; 2/15/2016; 3/16/2016; 6/30/2016; LOT CODES: 33644A0220; 32274A0201; 32284A0201; 32584A0201; CODE FORMAT: EXAMPLE CODE: 33554B0211 3=LYNDEN PLANT 355=JULIAN DATE FOR DATE OF PRODUCTION 4=2014( YEAR) B= SHIFT ( AFTERNOON) 02=LINE# 11=MACHINE OPERATOR #
Quantity recalled4401 cases (4/35 oz. packages per case)

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-2088-2015
FDA event ID
70299
Recalling firm
Inventure Foods, Phoenix, AZ
Brand
Rader
Classification
Class II
Status
Terminated
Recall initiated
17 Jan 2015
FDA classified
28 Apr 2015
Reported
6 May 2015
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Listeria
Product category
Other

Timeline

17 Jan 2015Recall initiated by company
28 Apr 2015Classified by FDA+101 days
6 May 2015Published in enforcement report+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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

Listeria monocytogenes can grow at refrigerator temperatures. Infection is most dangerous for pregnant women, newborns, older adults and people with weakened immune systems. Symptoms can appear up to 70 days after eating contaminated food.

Product as listed by the FDA

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

Where it was distributed

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.

AlaskaArizonaCaliforniaColoradoIdahoMontanaNew MexicoNevadaOregonTexasUtahWashingtonWyoming

Stores named: Walmart

Questions about this recall

Why was it recalled?

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

Which lots are affected?

BEST BY DATES: 6/30/2016; 2/14/2016; 2/15/2016; 3/16/2016; 6/30/2016; LOT CODES: 33644A0220; 32274A0201; 32284A0201; 32584A0201; CODE FORMAT: EXAMPLE CODE: 33554B0211 3=LYNDEN PLANT 355=JULIAN DATE FOR DATE OF PRODUCTION 4=2014( YEAR) B= SHIFT ( AFTERNOON) 02=LINE# 11=MACHINE OPERATOR #

Where was it sold?

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.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

2 other products · FDA event 70299

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