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Class I: serious health riskTerminated

Request Foods GFS Cheese Manicotti in tomato sauce Recall

GFS Cheese Manicotti in tomato sauce

Request Foods Inc. · Holland, MI

Risk level
Class I
Reported by FDA
Dec 21, 2016
Recall ID
F-0723-2017
Check your lot numberHow we source this data

Summary

Request Foods recalled GFS Cheese Manicotti in tomato sauce starting Nov 15, 2016. The FDA classified it as Class I (serious health risk) and published enforcement report F-0723-2017 on Dec 21, 2016. Reason: Undeclared Eggs. Status: Terminated.

Why it was recalled

Undeclared Eggs

Product description

GFS Cheese Manicotti in tomato sauce. retail 68 oz. pan. 4 retail units per case

Lot numbers, UPCs & expiration codes

lot code 15268 UPC 9390121983 order number 219835

Where it was sold

MI, OH, FL, KY

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-0723-2017
Classification
Class I
Status
Terminated
Recall initiated
Nov 15, 2016
FDA report date
Dec 21, 2016
Quantity
1592 cases
Recall type
Voluntary: Firm initiated
Recalling firm
Request Foods Inc.

Original FDA data

Every field from FDA enforcement report F-0723-2017, exactly as published.

Show all FDA fields
City
Holland
State
MI
Status
Terminated
Country
United States
Event ID
75726
Address
3460 John F Donnelly Dr
Code information
lot code 15268 UPC 9390121983 order number 219835
Postal code
49424-9294
Report date
Dec 21, 2016
Product type
Food
Recall number
F-0723-2017
Classification
Class I
Recalling firm
Request Foods Inc.
Product quantity
1592 cases
Termination date
Jul 5, 2017
Reason for recall
Undeclared Eggs
Voluntary / mandated
Voluntary: Firm initiated
Product description
GFS Cheese Manicotti in tomato sauce. retail 68 oz. pan. 4 retail units per case
Distribution pattern
MI, OH, FL, KY
Recall initiation date
Nov 15, 2016
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Dec 15, 2016

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-0723-2017, published Dec 21, 2016. View the source record (openFDA) · FDA enforcement reports

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

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