FDA recall record

Aroma Imports Nabelsi Thyme recall — FDA F-2180-2017

Elevated lead levels in product

Class Iclassification
F-2180-2017official record ID
May 10, 2017report date

Recall record at a glance

Official recordF-2180-2017
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmAroma Imports Inc.
Report dateMay 10, 2017
Recall initiation dateMar 17, 2017
Quantity95 cases of 24(450g), 10 cases of 2 bags(4.5kg)
LocationDearborn Heights, MI, United States

Official product description

Nabelsi Thyme (also known on invoices as Zatar) 450g retail (24 packages per wholesale case) 4.5kg retail (2 bags per wholesale case) Cardboard box wholesale case, retail packages flexible plastic

Why the product was recalled

Elevated lead levels in product

Distribution information

Illinois, Michigan, Ohio, Virginia, and New Jersey

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: Press Release.

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.