Dried Longan Pulp- Made in China, 8oz(227g), GROWLAND INC. rear panel- Organic Planted, Store in cool and dry place, Ma
Summary
The FDA issued a Class II for Dried Longan Pulp- Made in China, 8oz(227g), GROWLAND INC. rear panel- Organic by Growland Inc. Reason: Elevated levels of Sulfites in Dried Longan Pulp.
Details
Source
Food Recall
External ID
F-0648-2025
Action Date
2025-03-26
Status
Ongoing
Category
food
Product Description
Dried Longan Pulp- Made in China, 8oz(227g), GROWLAND INC. rear panel- Organic Planted, Store in cool and dry place, Made in Thailand; UPC# 8 513041 327262
Lot/Code Info: Exp: 09.30.2028
Quantity Affected: 957 cases
Reason for Recall
Elevated levels of Sulfites in Dried Longan Pulp
Distribution
Product was distributed to customers in CA, TX, WA, OR, AZ, FL, NV
Type: Voluntary: Firm initiated
Recall Initiated: 2025-02-18
Company
Chino, CA
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 53 food recalls issued in the same week, part of 204 food-related FDA actions this month.
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 (Growland Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Growland Inc have FDA actions?
This is the only FDA action we have on record for Growland Inc in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0648-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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