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CriticalFDAfda-F-0212-2016SALMONELLA CONTAMINATION

Raw cucumbers packaged in bulk in 6-count corrugated boxes bearing the Front Row Produce logo. There is no city or state listed on the l...

⚠ 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.

Category
Units Affected
165
Recall Date
September 4, 2015
Issuing Agency
Hazard
Salmonella Contamination

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0212-2016.

Potentially contaminated with Salmonella

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0212-2016.

Recall terminated by FDA.

✅ What you should do

  1. Stop using the product if you own it.
  2. Check the model number, lot code, or sell-by date against the recall notice above.
  3. Contact Front Row Produce Llc or the retailer where you bought it for a refund, replacement, or repair.
  4. For the most current official instructions, visit the FDA recall page.
  5. 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-0212-2016.

Front Row Produce LLC

FDA

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The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.

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📣 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.

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Front Row Produce Llc Recall FAQ

Front Row Produce Llc is the subject of a produce safety report: Raw cucumbers packaged in bulk in 6-count corrugated boxes bearing the Front Row Produce logo. There is no city or state listed on the l.... The notice was published on September 4, 2015 by the U.S. Food and Drug Administration (FDA). Approximately 165 units are potentially affected.