Bix Produce — FDA Recall History & Enforcement Records
Data Notice: Recall frequency varies by category and firm size; data is comparative and may not indicate actual brand safety or quality. See Methodology.
As of July 16, 2026, Bix Produce has 4 recorded FDA food enforcement actions in the openFDA database. Their most recent recall was on 29 Sep 2023. Bix Produce is categorized under Produce based on their predominant recall history.
Recall activity over time for Bix Produce
How serious are Bix Produce recalls?
FDA recall classifications by severity
Full FDA recall history for Bix Produce
All 4 FDA enforcement actions sourced from openFDA · Sorted by date, most recent first
| Date | Product | Reason | Class & Status |
|---|---|---|---|
| 29 Sep 2023Official FDA Notice | FreshPoint Bix Produce Company, Cantaloupe. Item # 03143. 3 melons per bag. | Cantaloupe may be contaminated with Salmonella. | Class ITerminated |
| 3 Jun 2022Official FDA Notice | Bix Produce Diced Spinach, Item # 15939. packaged in 2lb bags, with 5 bags per case | Foreign object – plastic | Class IITerminated |
| 24 May 2022Official FDA Notice | Egg &Cheese Curd Snack/Power Box. Cheese Curds, Hard-Cooked Egg, Apple Wedges, Peanut Butter & Lettuce. Keep Refrigera | Potential Salmonella contamination. | Class ITerminated |
| 21 Oct 2021Official FDA Notice | Raw onion sold in bags or sliced and diced with the following item numbers and lot code. 1. RED JUMBO 25# 1/25 LB, | Onions may be contaminated with Salmonella | Class ITerminated |
Where have Bix Produce recalls occurred?
States affected across all recorded FDA enforcement actions
Where does this recall data come from?
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Data sourced from the FDA Recall Enterprise System via openFDA API. This information is for educational purposes only and does not constitute health or legal advice. FoodRecallFinder.com is not affiliated with or endorsed by the U.S. Food and Drug Administration.
To determine if your specific product is affected, verify that the brand name, product description, lot number, UPC code, and date range all match the recall details exactly. When in doubt contact the recalling firm or visit FDA.gov.
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