CLASS II ONGOING Food recall · Reported 26 Mar 2025 · FDA Enforcement Report
Dried Longan Pulp recalled by Growland
Growland is recalling Dried Longan Pulp, distributed in 7 states. The recall was initiated on 18 Feb 2025 and the FDA has classified it as Class II.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-0648-2025
- FDA event ID
- 96264
- Recalling firm
- Growland, Chino, CA
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 18 Feb 2025
- FDA classified
- 20 Mar 2025
- Reported
- 26 Mar 2025
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Undeclared Sulfites
- Product category
- Other
Timeline
| 18 Feb 2025 | Recall initiated by company | |
| 20 Mar 2025 | Classified by FDA | +30 days |
| 26 Mar 2025 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Elevated levels of Sulfites in Dried Longan Pulp
Product as listed by the FDA
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
Where it was distributed
Product was distributed to customers in CA, TX, WA, OR, AZ, FL, NV
Questions about this recall
Why was it recalled?
Elevated levels of Sulfites in Dried Longan Pulp
Which lots are affected?
Exp: 09.30.2028
Where was it sold?
Product was distributed to customers in CA, TX, WA, OR, AZ, FL, NV
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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