1 1/9 Bushel Limited Edition Cucumber Carton, Sizes: Plains (60-84 count), Extra Large (48 count), Large (60 count), Super Select (72 cou...
⚠ 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-0190-2016.
Andrew and Williamson Fresh Produce (A&W) is recalling all cucumbers sold under the Limited Edition label because it may be contaminated with Salmonella.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0190-2016.
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 Andrew & Williamson Fresh Produce 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-0190-2016.
Andrew & Williamson Fresh Produce
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.
Andrew & Williamson Fresh Produce Recall FAQ
Andrew & Williamson Fresh Produce is the subject of a food safety report: 1 1/9 Bushel Limited Edition Cucumber Carton, Sizes: Plains (60-84 count), Extra Large (48 count), Large (60 count), Super Select (72 cou.... The notice was published on September 4, 2015 by the U.S. Food and Drug Administration (FDA). Approximately 47,895 units are potentially affected.