Skip to main content
High RiskFDAfda-F-1952-2018CONTAMINATION

Sammy Salsa Roasted Cabo Verde, packaged in 14 oz. plastic container, 6 units per case. UPC # 00868422000141. The label is read in par...

Category
Units Affected
10
Recall Date
August 15, 2018
Issuing Agency
Hazard
Contamination

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1952-2018.

Salsa products are recalled due to a potential contamination with Cyclospora. Salsa products contain cilantro that was recalled due to a potential contamination with Cyclospora.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1952-2018.

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 Sammy Food Products 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-1952-2018.

Sammy Food Products LLC

FDA

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.

How to report to FDAFile a report at FDA

Sammy Food Products Llc Recall FAQ

Sammy Food Products Llc is the subject of a beverages safety report: Sammy Salsa Roasted Cabo Verde, packaged in 14 oz. plastic container, 6 units per case. UPC # 00868422000141. The label is read in par.... The notice was published on August 15, 2018 by the U.S. Food and Drug Administration (FDA). Approximately 10 units are potentially affected.