Cardboard sleeve: Cheese Club express mac Macaroni & Cheese Dinner, Four 2.05 OZ Bowls; Net Wt.…
Recalling firm: Fourth Street Barbeque, Inc.
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…
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: May 10, 2018.
Check your package
Compare the exact product and package details with the label you have.
FDA code information
Cheese Club: Best by: 10/18/2017 10/21/2017 10/22/2017; UPC: 41498171674;
Match the product, package size, and code together. A missing match does not guarantee safety.
Full FDA record and distribution details
Original 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
Extracted codes and context
| Type | Code / value | Context |
|---|---|---|
| best by | 10/18/2017 | Cheese Club: Best by: 10/18/2017 10/21/2017 10/22/2017; UPC: 41498171674; |
Original FDA recall 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 details
- Recall number
- F-1235-2017
- Event ID
- 75911
- FDA status
- Terminated
- Initiated
- Dec 9, 2016
- Reported
- Jan 18, 2017
- Classified
- Jan 11, 2017
- Terminated
- May 10, 2018
- Quantity
- 31,080 retail units
- Location
- Charleroi, PA, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Telephone
Where it was distributed
CA CT GA IL MS OK PA SC VA WA
Data updated September 16, 2026. View official FDA data ↗
Follow official FDA and manufacturer guidance.