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CriticalFDAfda-F-2032-2012LISTERIA

Fresh Whole Honey Dew Melons, packed in paper cartons labeled, Southeastern Growers Association, Fresh Melons. Individual melons were not...

⚠ Critical Alert — Stop Using Immediately

This product has been flagged with severe risks (listeria). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.

Category
Units Affected
0
Recall Date
July 28, 2012
Issuing Agency
Hazard
Listeria

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2032-2012.

Product was found to be contaminated with Listeria monocytogenes.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2032-2012.

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 Burch Farms 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-2032-2012.

Burch Farms

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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Burch Farms Recall FAQ

Burch Farms is the subject of a produce safety report: Fresh Whole Honey Dew Melons, packed in paper cartons labeled, Southeastern Growers Association, Fresh Melons. Individual melons were not.... The notice was published on July 28, 2012 by the U.S. Food and Drug Administration (FDA). Approximately 0 units are potentially affected.