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Class I: serious health riskTerminated

Nu Life Market Sun Life Natural Sunflower Kernel Paste Recall

Sun Life Natural Sunflower Kernel Paste

Nu Life Market LLC · Scott City, KS

Risk level
Class I
Reported by FDA
Aug 24, 2016
Recall ID
F-1925-2016
Check your lot numberHow we source this data

Summary

Nu Life Market recalled Sun Life Natural Sunflower Kernel Paste starting May 19, 2016. The FDA classified it as Class I (serious health risk) and published enforcement report F-1925-2016 on Aug 24, 2016. Reason: Product manufactured with roasted sunflower kernels which may be contaminated with Listeria monocytogenes. Status: Terminated.

Why it was recalled

Product manufactured with roasted sunflower kernels which may be contaminated with Listeria monocytogenes.

Product description

Sun Life Natural Sunflower Kernel Paste, Net Wt. 40 lbs (18.18 kg) buckets and 450 lbs. (204.12 kg) barrels. The responsible name on the label is Nu Life Market, LLC, Scott City, KS.

Lot numbers, UPCs & expiration codes

lot 5280D1, exp. 7/7/2016; lot 5281D1, exp. 7/8/2016; lot 5282D1, exp. 7/9/2016; lot 5285D1, exp. 7/12/2016; lot 5351D1, exp. 9/17/2016; lot 5352D1, exp. 9/18/2016; lot 5355D1, exp. 9/21/2016; lot 5356D1, exp. 9/22/2016; lot 6082D1, exp: 12/22/2016; lot 6076D1, exp: 12/16/2016; lot 6111D1, exp: 4/20/2017; lot 6112D1, exp: 4/21/2017; lot 6113D1, exp: 4/22/2017; and lot 6116D1, exp: 4/25/2017

Where it was sold

Product was distributed to CA, IL, and MI. There was no foreign/military/government distribution.

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-1925-2016
Classification
Class I
Status
Terminated
Recall initiated
May 19, 2016
FDA report date
Aug 24, 2016
Quantity
70,670 lbs.
Recall type
Voluntary: Firm initiated
Recalling firm
Nu Life Market LLC

Original FDA data

Every field from FDA enforcement report F-1925-2016, exactly as published.

Show all FDA fields
City
Scott City
State
KS
Status
Terminated
Country
United States
Event ID
74250
Address
1202 E 5th St
Code information
lot 5280D1, exp. 7/7/2016; lot 5281D1, exp. 7/8/2016; lot 5282D1, exp. 7/9/2016; lot 5285D1, exp. 7/12/2016; lot 5351D1, exp. 9/17/2016; lot 5352D1, exp. 9/18/2016; lot 5355D1, exp. 9/21/2016; lot 5356D1, exp. 9/22/2016; lot 6082D1, exp: 12/22/2016; lot 6076D1, exp: 12/16/2016; lot 6111D1, exp: 4/20/2017; lot 6112D1, exp: 4/21/2017; lot 6113D1, exp: 4/22/2017; and lot 6116D1, exp: 4/25/2017
Postal code
67871-4155
Report date
Aug 24, 2016
Product type
Food
Recall number
F-1925-2016
Classification
Class I
Recalling firm
Nu Life Market LLC
Product quantity
70,670 lbs.
Termination date
Sep 14, 2018
Reason for recall
Product manufactured with roasted sunflower kernels which may be contaminated with Listeria monocytogenes.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Sun Life Natural Sunflower Kernel Paste, Net Wt. 40 lbs (18.18 kg) buckets and 450 lbs. (204.12 kg) barrels. The responsible name on the label is Nu Life Market, LLC, Scott City, KS.
Distribution pattern
Product was distributed to CA, IL, and MI. There was no foreign/military/government distribution.
Recall initiation date
May 19, 2016
Initial firm notification
E-Mail
Center classification date
Aug 15, 2016

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1925-2016, published Aug 24, 2016. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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