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High RiskFDAfda-F-2389-2016LACERATION

Better Value Mix Vegetables, Federated Group, Inc./Arlington Heights, IL 60005-1096; 14 oz. pkgs; BB 05/06/18; Morning Fresh Farms Mix ...

Category
Units Affected
3,051
Recall Date
August 18, 2016
Issuing Agency
Hazard
Laceration

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2389-2016.

Firm was notified by North Carolina Dept. of Agriculture that a sample of Better Valu Cut Corn was found positive for Listeria monocytogenes. Firm initiated a recall based on the sample results.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2389-2016.

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 Cambridge Farms Of Hanover Llc D 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-2389-2016.

CAMBRIDGE FARMS OF HANOVER LLC D

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.

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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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Cambridge Farms Of Hanover Llc D Recall FAQ

Cambridge Farms Of Hanover Llc D is the subject of a produce safety report: Better Value Mix Vegetables, Federated Group, Inc./Arlington Heights, IL 60005-1096; 14 oz. pkgs; BB 05/06/18; Morning Fresh Farms Mix .... The notice was published on August 18, 2016 by the U.S. Food and Drug Administration (FDA). Approximately 3,051 units are potentially affected.