FDA Recall United States Terminated Historical recordClass I
U.S. Tov, Inc.
- Product
- Dragonfly Jelly Bar Handbag 11.64oz, 17.63oz UPC Code 721557…
- Published
- February 21, 2024
- Distribution
- U.S. distribution to the following: AK,…
U.S. Tov, Inc. Recall: New York State Dept of Agriculture and Markets tested Galanga Powder and found it to contain lead.
United States
TerminatedClass II
- Company
- U.S. Tov, Inc.
- Product
- Dragonfly brand Galanga Powder; Net Weight: 5 oz. (142 g)…
- Recall date
- May 15, 2020
- Terminated
- July 6, 2020
- Source
- FDA
Reason for recall
New York State Dept of Agriculture and Markets tested Galanga Powder and found it to contain lead.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Dragonfly brand Galanga Powder; Net Weight: 5 oz. (142 g) UPC: 7 21557 53337 6 Product of Thailand Distributed by U.S. Trading Company, Hayward, CA 94545-1130 | Not published in this source record | 100 cases | Lot #078 MBI; Expiration: 3/18/21. |
Distribution
- AK
- AR
- CA
- CO
- FL
- GA
- IA
- IN
- KS
- LA
- MN
- MO
- NC
- NE
- NV
- NY
- OR
- SC
- SD
- TX
- UT
- VA
- WA
- WI
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0975-2020
- Event ID
- 85699
- Status
- Terminated
- Classification
- Class II
- Company
- U.S. Tov, Inc.
- Product description
- Dragonfly brand Galanga Powder; Net Weight: 5 oz. (142 g) UPC: 7 21557 53337 6 Product of Thailand Distributed by U.S. Trading Company, Hayward, CA 94545-1130
- Quantity
- 100 cases
- Reason
- New York State Dept of Agriculture and Markets tested Galanga Powder and found it to contain lead.
- Recall initiation date
- May 15, 2020
- Report date
- June 10, 2020
- Classification date
- Not published in this source record
- Termination date
- July 6, 2020
- Distribution pattern
- AK, AR, CA, CO, FL, GA, IA, IN, KS, LA, MN, MO, NC, NE, NV, NY, OR, SC, SD, TX, UT, VA, WA, WI
- UPC, lot, and code information
- Lot #078 MBI; Expiration: 3/18/21.
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Letter
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: U.S. Tov, Inc.
Other recalls from U.S. Tov, Inc.
FDA Recall United States Terminated Historical recordClass I
U.S. Tov, Inc.
- Product
- Global Pride Rattan Shoots in Brine: 24 oz. glass jar UPC:…
- Published
- June 5, 2019
- Distribution
- Multiple states
FDA Recall United States Terminated Historical recordClass III
U.S. Tov, Inc.
- Product
- Dragonfly Dehydrate Guava Ing: Guava, Sugar, Salt Net Wt:…
- Published
- May 15, 2019
- Distribution
- U.S. distribution to the following: AK,…
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Alaska | 1 |
| Arkansas | 1 |
| California | 1 |
| Colorado | 1 |
| Florida | 1 |
| Georgia | 1 |
| Iowa | 1 |
| Indiana | 1 |
| Kansas | 1 |
| Louisiana | 1 |
| Minnesota | 1 |
| Missouri | 1 |
| North Carolina | 1 |
| Nebraska | 1 |
| Nevada | 1 |
| New York | 1 |
| Oregon | 1 |
| South Carolina | 1 |
| South Dakota | 1 |
| Texas | 1 |
| Utah | 1 |
| Virginia | 1 |
| Washington | 1 |
| Wisconsin | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
