BELEVINI, DRIED FRUIT MIX (Apples, Pears & Plums w/pit), 500g, PLASTIC SOFT PACK, 6 PACKAGES PER CASE
Summary
The FDA issued a Class II for BELEVINI, DRIED FRUIT MIX (Apples, Pears & Plums w/pit), 500g, PLASTIC SOFT PACK by MAMTAKIM, Inc.. Reason: Product contains undeclared sulfites. The product was sampled by the NYSAGM s Food Safety Division and tested positive at 120.7 PPM Sulfites..
Details
Source
Food Recall
External ID
F-0142-2025
Action Date
2024-11-27
Status
Terminated
Category
food
Product Description
BELEVINI, DRIED FRUIT MIX (Apples, Pears & Plums w/pit), 500g, PLASTIC SOFT PACK, 6 PACKAGES PER CASE
Lot/Code Info: PRODUCT NUMBER - MCL3919 , BAR CODE # - 4840801000337
Quantity Affected: 109 cases
Reason for Recall
Product contains undeclared sulfites. The product was sampled by the NYSAGM s Food Safety Division and tested positive at 120.7 PPM Sulfites.
Distribution
The recalled product was distributed to NY, NJ
Type: Voluntary: Firm initiated
Recall Initiated: 2024-10-25
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 25 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-0142-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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