Recall record at a glance
| Official record | F-1116-2017 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Sabra Dipping Company, LLC |
| Report date | Jan 18, 2017 |
| Recall initiation date | Nov 18, 2016 |
| Quantity | 110349 Cases |
| Location | South Chesterfield, VA, United States |
Official product description
Sabra Hummus Spinach/Art, 10 OZ, 17 OZ, 32OZ UPC SKU ITEM 040822027700 300266 Sabra Hummus Spinach/Art 32OZ 040822027588 300298 Sabra Hummus Spinach/Art 17OZ 040822027540 300164 Sabra Hummus Spinach/Art 10OZ
Why the product was recalled
Products have the potential to be contaminated with Listeria monocytogenes.
Distribution information
Thru out the US and three foreign countries.
How to read the classification
FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.
FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.