FDA recall record

MAMTAKIM Scortisoara macinata/ Ground cinnamon, 15 g, Paper cartons, 20 recall — FDA F-1779-2024

MAMTAKIM Inc.,888 Magnolia Ave, Elizabeth NJ 07201 is initiating a recall of Scortisoara macinata/ Ground cinnamon, 15 g, Paper cartons, 20 pieces per…

Class IIclassification
F-1779-2024official record ID
Sep 11, 2024report date

Recall record at a glance

Official recordF-1779-2024
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmMAMTAKIM, Inc.
Report dateSep 11, 2024
Recall initiation dateJul 29, 2024
Quantity30 Cases = 640 pieces
LocationElizabeth, NJ, United States

Official product description

Scortisoara macinata/ Ground cinnamon, 15 g, Paper cartons, 20 pieces per paper carton

Why the product was recalled

MAMTAKIM Inc.,888 Magnolia Ave, Elizabeth NJ 07201 is initiating a recall of Scortisoara macinata/ Ground cinnamon, 15 g, Paper cartons, 20 pieces per paper carton, Code: 10C035 because the ground cinnamon product contain elevated levels of lead .

Distribution information

The recalled product was distributed to the following States: FL, CT, GA, CA, TN, PA, OH, NY, SC

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

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.

Related recall records

Other records from the same recalling company are shown first when available.