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CriticalFDAfda-F-2070-2019LISTERIA

Archer Farms egg salad packaged in 12oz plastic cup with lid, 6 cups per case, refrigerated

⚠ 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
572
Recall Date
July 19, 2019
Issuing Agency
Hazard
Listeria

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2070-2019.

Listeria monocytogenes was found in egg salad produced by the firm. In abundance of caution, firm is recalling all product produced on the same line on the same date.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2070-2019.

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 Elevation Foods 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-2070-2019.

Elevation Foods

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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Elevation Foods Recall FAQ

Elevation Foods is the subject of a produce safety report: Archer Farms egg salad packaged in 12oz plastic cup with lid, 6 cups per case, refrigerated. The notice was published on July 19, 2019 by the U.S. Food and Drug Administration (FDA). Approximately 572 units are potentially affected.