Fat Boy Fresh Produce - cucumbers. Cucumbers are often referred to as Slicer or American cucumber and are 7-10 inches long ang 1.75 to 2...
⚠ Critical Alert — Stop Using Immediately
This product has been flagged with severe risks (Salmonella contamination). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0210-2016.
Cucumbers received from direct supplier and currently under recall for potential Salmonella contamination were repacked and distributed under a different brand name..
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0210-2016.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact Custom Produce Sales or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- If you've been hurt by this product, report the incident to FDA.
Consumer Contact (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0210-2016.
Custom Produce Sales
About the U.S. Food and Drug Administration
The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.
Visit FDA.gov →📣 Report a food, supplement, or cosmetic problem to the FDA
If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.
Custom Produce Sales Recall FAQ
Custom Produce Sales is the subject of a produce safety report: Fat Boy Fresh Produce - cucumbers. Cucumbers are often referred to as Slicer or American cucumber and are 7-10 inches long ang 1.75 to 2.... The notice was published on September 4, 2015 by the U.S. Food and Drug Administration (FDA). Approximately 2,175 units are potentially affected.