FRESH TO GO Mediterranean Chicken with Hummus sandwich, close-face ready-to-eat sandwich, refrigerated, packed in plastic clam shell, net...
⚠ 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.
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0750-2017.
Mediterranean Chicken with Hummus ready to eat sandwich, refrigerated product, is recalled due to a potential contamination with Listeria monocytogenes. The sandwich contains the affected Roasted Red Pepper Hummus which was recalled by Sabra Dipping Co., LLC.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0750-2017.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact Lsg Sky Chefs, Inc. or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- 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-0750-2017.
LSG Sky Chefs, Inc.
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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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.
Lsg Sky Chefs, Inc. Recall FAQ
Lsg Sky Chefs, Inc. is the subject of a meat & poultry safety report: FRESH TO GO Mediterranean Chicken with Hummus sandwich, close-face ready-to-eat sandwich, refrigerated, packed in plastic clam shell, net.... The notice was published on November 20, 2016 by the U.S. Food and Drug Administration (FDA). Approximately 103 units are potentially affected.