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Class I: serious health riskTerminated

SunBurst Foods Ham Omelet with Dinner Roll Recall

Ham Omelet with Dinner Roll

SunBurst Foods, Inc. · Goldsboro, NC

Risk level
Class I
Reported by FDA
Feb 4, 2015
Recall ID
F-0914-2015
Check your lot numberHow we source this data

Summary

SunBurst Foods recalled Ham Omelet with Dinner Roll starting Oct 10, 2014. The FDA classified it as Class I (serious health risk) and published enforcement report F-0914-2015 on Feb 4, 2015. Reason: Listeria monocytogenes. Status: Terminated.

Why it was recalled

Listeria monocytogenes

Product description

Ham Omelet with Dinner Roll, Net Wt. 5.80 oz., UPC 7-01248-00855-0, MFG Code 1582

Lot numbers, UPCs & expiration codes

See product description for lot numbers

Where it was sold

NC, NJ & SC

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-0914-2015
Classification
Class I
Status
Terminated
Recall initiated
Oct 10, 2014
FDA report date
Feb 4, 2015
Quantity
N/A
Recall type
Voluntary: Firm initiated
Recalling firm
SunBurst Foods, Inc.

Original FDA data

Every field from FDA enforcement report F-0914-2015, exactly as published.

Show all FDA fields
City
Goldsboro
State
NC
Status
Terminated
Country
United States
Event ID
69555
Address
1002B Sunburst Dr
Code information
See product description for lot numbers
Postal code
27534-8667
Report date
Feb 4, 2015
Product type
Food
Recall number
F-0914-2015
Classification
Class I
Recalling firm
SunBurst Foods, Inc.
Termination date
Jun 18, 2015
Reason for recall
Listeria monocytogenes
Voluntary / mandated
Voluntary: Firm initiated
Product description
Ham Omelet with Dinner Roll, Net Wt. 5.80 oz., UPC 7-01248-00855-0, MFG Code 1582
Distribution pattern
NC, NJ & SC
Recall initiation date
Oct 10, 2014
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Jan 26, 2015

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-0914-2015, published Feb 4, 2015. View the source record (openFDA) · FDA enforcement reports

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

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