Lian Sheng Dried Plum; 5.8oz (165g); packaged in clear plastic bottle; UPC 6928580581396
Summary
The FDA issued a Class II for Lian Sheng Dried Plum; 5.8oz (165g); packaged in clear plastic bottle; UPC 69285 by Rong Shing Trading NY Inc. Reason: Product contains high levels of undeclared sulfites (21.91 mg/serving)..
Details
Source
Food Recall
External ID
F-1034-2024
Action Date
2024-03-13
Status
Terminated
Category
food
Product Description
Lian Sheng Dried Plum; 5.8oz (165g); packaged in clear plastic bottle; UPC 6928580581396
Lot/Code Info: Expiration date of 11/13/2023 stamped on the side.
Reason for Recall
Product contains high levels of undeclared sulfites (21.91 mg/serving).
Distribution
Florida and New York
Type: Voluntary: Firm initiated
Recall Initiated: 2023-12-14
Company
Brooklyn, NY
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 124 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Rong Shing Trading NY Inc has 6 FDA actions in our database, including 6 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 (Rong Shing Trading NY Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Rong Shing Trading NY Inc have FDA actions?
Rong Shing Trading NY Inc has 6 FDA actions in our database, including 6 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1034-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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