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High RiskFDAfda-F-2365-2017OTHER

Bright Farms Baby Romaine - 4oz package , The salad products packaged in clear, plastic clamshells with best by dates on the package .

Category
Units Affected
300
Recall Date
May 17, 2017
Issuing Agency
Hazard
Other

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2365-2017.

According to the firm, they have detected metal in their product. The firm learned of the problem through an internal verification techniques. The firm believes there is a risk of a health hazard. an is enacting this recall.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2365-2017.

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 Brightfarms, Inc.: Wdc Greenhouse 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-2365-2017.

BrightFarms, Inc.: WDC Greenhouse 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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Brightfarms, Inc.: Wdc Greenhouse Llc Recall FAQ

Brightfarms, Inc.: Wdc Greenhouse Llc is the subject of a produce safety report: Bright Farms Baby Romaine - 4oz package , The salad products packaged in clear, plastic clamshells with best by dates on the package .. The notice was published on May 17, 2017 by the U.S. Food and Drug Administration (FDA). Approximately 300 units are potentially affected.