Scortisoara macinata/ Ground cinnamon, 15 g, Paper cartons, 20 pieces per paper carton
Summary
The FDA issued a Class II for Scortisoara macinata/ Ground cinnamon, 15 g, Paper cartons, 20 pieces per paper by MAMTAKIM, Inc.. Reason: MAMTAKIM Inc.,888 Magnolia Ave, Elizabeth NJ 07201 is initiating a recall of Scortisoara macinata/ Ground cinnamon, 15 g, Paper cartons, 20 pieces pe.
Details
Source
Food Recall
External ID
F-1779-2024
Action Date
2024-09-11
Status
Terminated
Category
food
Product Description
Scortisoara macinata/ Ground cinnamon, 15 g, Paper cartons, 20 pieces per paper carton
Lot/Code Info: Internal Product code :10C035 L1205231
Quantity Affected: 30 Cases = 640 pieces
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 .
Distribution
The recalled product was distributed to the following States: FL, CT, GA, CA, TN, PA, OH, NY, SC
Type: Voluntary: Firm initiated
Recall Initiated: 2024-07-29
Company
Elizabeth, NJ
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 49 food recalls issued in the same week, part of 204 food-related FDA actions this month.
MAMTAKIM, Inc. has 4 FDA actions in our database, including 4 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (MAMTAKIM, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does MAMTAKIM, Inc. have FDA actions?
MAMTAKIM, Inc. has 4 FDA actions in our database, including 4 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1779-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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