“Garden Fresh Potato Salad Kit Recalled for Listeria Risk.” GovInfoNow, updated October 12, 2026. https://govinfonow.com/recall/26778-garden-fresh-steakhouse-potato-salad-kit-recall-listeria-risk. Based on FDA recall #F-2816-2015 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2816-2015%22&limit=1).
The FDA announced on June 10, 2015, that Garden Fresh Foods, Inc. voluntarily recalled its Steakhouse Potato Salad Kit due to a presumptive positive test for Listeria monocytogenes. The recall affects 400 cases distributed in Illinois.
How to tell if you have it
Brand: Garden Fresh
Product: Steakhouse Potato Salad Kit
Code: CODE#1076
Net Weight: 10.75 LBS (4.876 KG)
UPC: 0 01 11596 51076 4
Production Order: 070615 (PO 78432885)
The hazard
Garden Fresh Foods, Inc. reported one case of the Steakhouse Potato Salad Kit tested presumptive for Listeria monocytogenes. The FDA classified the recall as Class I.
Context
GovInfoNow's records show Garden Fresh Foods, Inc. has had five other recalls on record since November 7, 2013. Other recent recalls of similar products include a September 18, 2025 recall of sliced green onions due to possible Listeria contamination and a February 7, 2022 Weis Potato Salad Recall for undeclared milk. Similar recent recalls include Made Fresh Salads Vegetable Cream Cheese, Garlic & Herb Cream Cheese, and Sundried Tomato Cream Cheese recalls announced on February 19, 2026, all citing Listeria contamination risk.
How to tell if you have this one
Check your product for CODE#1076 and UPC 0 01 11596 51076 4. The package contains NET WT 10.75 LBS (4.876 KG). The production order number is PO 78432885.
Brand
Garden Fresh
Product
Garden-Fresh Foods, Inc. recalls Garden Fresh Steakhouse Potato Salad Kit, CODE#1076, NET WT 10.75 LBS (4.876 KG) , UPC 0 01 11596 51076 4
Category
Food
Based on the official FDA remedy
What to do — step by step
Stop consuming the product
Do not eat the Steakhouse Potato Salad Kit if you have CODE#1076 and UPC 0 01 11596 51076 4.
Discard or return the item
The record does not specify a remedy, so you should dispose of the product or contact the retailer for guidance.
Where it went and when
Where it was distributed
Distributed in Illinois.
Listed by the agency
Not listed
FDA distribution: “IL” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Illinois.
Recall timeline
FDA terminated this recall 9 months after the firm started it.
1Firm started the recall
2FDA classified it Class I
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #F-2816-2015 (June 10, 2015) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2816-2015 to see it in context.
Plain-language summary written by qwen3.6:35b-a3b on October 12, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.