FDA Recall United States Terminated Historical recordClass I
MAMTAKIM, Inc.
- Product
- Belevini BICHKI, Dried Salted Whole Smelts, Net. Weight, 5.2…
- Published
- December 24, 2025
- Distribution
- The adulterated product was distributed…
MAMTAKIM, Inc. Recall: 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 .
United States
TerminatedClass II
- Company
- MAMTAKIM, Inc.
- Product
- Scortisoara macinata/ Ground cinnamon, 15 g, Paper cartons,…
- Recall date
- July 29, 2024
- Terminated
- September 30, 2024
- Source
- FDA
Reason for recall
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 .
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Scortisoara macinata/ Ground cinnamon, 15 g, Paper cartons, 20 pieces per paper carton | Not published in this source record | 30 Cases = 640 pieces | Internal Product code :10C035 L1205231 |
Distribution
- The recalled product was distributed to the following States: FL
- CT
- GA
- CA
- TN
- PA
- OH
- NY
- SC
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1779-2024
- Event ID
- 95134
- Status
- Terminated
- Classification
- Class II
- Company
- MAMTAKIM, Inc.
- Product description
- Scortisoara macinata/ Ground cinnamon, 15 g, Paper cartons, 20 pieces per paper carton
- Quantity
- 30 Cases = 640 pieces
- Reason
- 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 .
- Recall initiation date
- July 29, 2024
- Report date
- September 11, 2024
- Classification date
- Not published in this source record
- Termination date
- September 30, 2024
- Distribution pattern
- The recalled product was distributed to the following States: FL, CT, GA, CA, TN, PA, OH, NY, SC
- UPC, lot, and code information
- Internal Product code :10C035 L1205231
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: MAMTAKIM, Inc.
Other recalls from MAMTAKIM, Inc.
FDA Recall United States Terminated Historical recordClass I
MAMTAKIM, Inc.
- Product
- Belevini KORUSHKA, Dried Salted Whole Smelts, Net. Weight, 5…
- Published
- December 24, 2025
- Distribution
- The adulterated product was distributed…
FDA Recall United States Terminated Historical recordClass II
MAMTAKIM, Inc.
- Product
- BELEVINI, DRIED FRUIT MIX (Apples, Pears & Plums w/pit), 500…
- Published
- November 27, 2024
- Distribution
- The recalled product was distributed to…
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Florida | 1 |
| Connecticut | 1 |
| Georgia | 1 |
| California | 1 |
| Tennessee | 1 |
| Pennsylvania | 1 |
| Ohio | 1 |
| New York | 1 |
| South Carolina | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
