Skip to main content
High RiskFDAfda-F-0399-2019SALMONELLA CONTAMINATION

Love The Wild Hawaiian Style Tropical Bowl with Barramundi 9oz. UPC 50068 00602 Frozen 6, 9oz. units per case

Category
Units Affected
4,413
Recall Date
October 15, 2018
Issuing Agency
Hazard
Salmonella Contamination

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0399-2019.

The firm was notified by their supplier that ingredients used in their products were possibly contaminated with Listeria monocytogenes and Salmonella.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0399-2019.

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 Request Foods Incorporated 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-0399-2019.

Request Foods Incorporated

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

Request Foods Incorporated Recall FAQ

Request Foods Incorporated is the subject of a frozen food safety report: Love The Wild Hawaiian Style Tropical Bowl with Barramundi 9oz. UPC 50068 00602 Frozen 6, 9oz. units per case. The notice was published on October 15, 2018 by the U.S. Food and Drug Administration (FDA). Approximately 4,413 units are potentially affected.