Sabra Roasted Garlic Hummus, Classic Hummus packed in 2/23.5 oz plastic tub/package. UPC 040822342209, Sabra Dipping Co. LLC, White Plain...
⚠ Critical Alert — Stop Using Immediately
This product has been flagged with severe risks (other). 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-2086-2015.
Michigan Dept. of Agriculture collected a sample of Sabra Hummus that came up positive for L. Monocytogenes. Baltimore District is working with VDACS to investigate.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2086-2015.
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 Sabra Dipping Company, Llc 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-2086-2015.
Sabra Dipping Company, LLC
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.
Visit FDA.gov →📣 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.
Sabra Dipping Company, Llc Recall FAQ
Sabra Dipping Company, Llc is the subject of a food safety report: Sabra Roasted Garlic Hummus, Classic Hummus packed in 2/23.5 oz plastic tub/package. UPC 040822342209, Sabra Dipping Co. LLC, White Plain.... The notice was published on April 7, 2015 by the U.S. Food and Drug Administration (FDA). Approximately 796 units are potentially affected.