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CriticalFDAfda-F-0578-2017SALMONELLA CONTAMINATION

Chicken eggs packaged in the following configurations 1) Premium Farm Fresh White Eggs, packaged in 6 count, 10 count, 12 count, and 1...

⚠ Critical Alert — Stop Using Immediately

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

Units Affected
59,129
Recall Date
October 1, 2016
Issuing Agency
Hazard
Salmonella Contamination

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0578-2017.

Eggs may be contaminated with Salmonella Oranienburg

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0578-2017.

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 Good Earth Egg Company 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-0578-2017.

Good Earth Egg Company

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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Good Earth Egg Company Recall FAQ

Good Earth Egg Company is the subject of a meat & poultry safety report: Chicken eggs packaged in the following configurations 1) Premium Farm Fresh White Eggs, packaged in 6 count, 10 count, 12 count, and 1.... The notice was published on October 1, 2016 by the U.S. Food and Drug Administration (FDA). Approximately 59,129 units are potentially affected.