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Fourth Street Barbeque, Inc. Recall: Fourth Street Barbecue Inc./ Packing Division has initiated the voluntary recall of Cheese Club Express Mac & Cheese 4 cup dinner and Double Takes Macaroni & Cheese 2 cup dinner due to possible health risk. The powdered cheese packets may be impacted by milk powder ingredients recalled by Valley Milk Products, LLC contaminated with Salmonella.

United States

TerminatedClass II

Company
Fourth Street Barbeque, Inc.
Product
Cardboard sleeve: Cheese Club express mac Macaroni & Cheese…
Recall date
December 9, 2016
Terminated
May 10, 2018
Source
FDA

Reason for recall

Fourth Street Barbecue Inc./ Packing Division has initiated the voluntary recall of Cheese Club Express Mac & Cheese 4 cup dinner and Double Takes Macaroni & Cheese 2 cup dinner due to possible health risk. The powdered cheese packets may be impacted by milk powder ingredients recalled by Valley Milk Products, LLC contaminated with Salmonella.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Cardboard sleeve: Cheese Club express mac Macaroni & Cheese Dinner, Four 2.05 OZ Bowls; Net Wt. 8.2 OZ.; Distributed by: Aldi, Inc., Batavia, IL 60510 Not published in this source record 31,080 retail units Cheese Club: Best by: 10/18/2017 10/21/2017 10/22/2017; UPC: 41498171674;

Distribution

  • CA CT GA IL MS OK PA SC VA WA

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-1235-2017
Event ID
75911
Status
Terminated
Classification
Class II
Company
Fourth Street Barbeque, Inc.
Product description
Cardboard sleeve: Cheese Club express mac Macaroni & Cheese Dinner, Four 2.05 OZ Bowls; Net Wt. 8.2 OZ.; Distributed by: Aldi, Inc., Batavia, IL 60510
Quantity
31,080 retail units
Reason
Fourth Street Barbecue Inc./ Packing Division has initiated the voluntary recall of Cheese Club Express Mac & Cheese 4 cup dinner and Double Takes Macaroni & Cheese 2 cup dinner due to possible health risk. The powdered cheese packets may be impacted by milk powder ingredients recalled by Valley Milk Products, LLC contaminated with Salmonella.
Recall initiation date
December 9, 2016
Report date
January 18, 2017
Classification date
Not published in this source record
Termination date
May 10, 2018
Distribution pattern
CA CT GA IL MS OK PA SC VA WA
UPC, lot, and code information
Cheese Club: Best by: 10/18/2017 10/21/2017 10/22/2017; UPC: 41498171674;
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Telephone
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Other products recalled under this same event

This recall shares FDA event ID 75911 with 1 other product entry in Public Health Trace.

FDA Recall United States Terminated Historical recordClass II

Fourth Street Barbeque, Inc.

Product
Cardboard sleeve: Double Takes Macaroni & Cheese Dinner, Dis…
Published
January 18, 2017
Distribution
CA CT GA IL MS OK PA SC VA WA

View recall →

Responsible company: Fourth Street Barbeque, Inc.

Other recalls from Fourth Street Barbeque, Inc.

FDA Recall United States Terminated Historical recordClass II

Fourth Street Barbeque, Inc.

Product
Pick 5 Chicken & Waffle Sandwich; Mix & Match, Keep Frozen;…
Published
June 14, 2017
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Fourth Street Barbeque, Inc.

Product
Cardboard sleeve: Double Takes Macaroni & Cheese Dinner, Dis…
Published
January 18, 2017
Distribution
CA CT GA IL MS OK PA SC VA WA

View recall →

Distribution map

A map highlighting the states named in the source's distribution description.

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map
State Distributed
California 1
Connecticut 1
Georgia 1
Illinois 1
Mississippi 1
Oklahoma 1
Pennsylvania 1
South Carolina 1
Virginia 1
Washington 1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.