Recall record at a glance
| Official record | F-2847-2015 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Lion Pavilion Ltd. |
| Report date | Jul 22, 2015 |
| Recall initiation date | Feb 22, 2013 |
| Quantity | UNKNOWN |
| Location | Maspeth, NY, United States |
Official product description
Grassplot Ginger Slice, NET WT. 3.5 OZ. (100g) , UPC 7246 6247, PRODUCT OF CHINA --- Firms on label: Manufactory: Grassplot Foodstuff Factory ADD: Huangshan Road, Huangshan Mansion, suite 417 Shantou, Guangdong, China -- Distributed by: LION PAVILION LIMITED --- Nutrition Facts: Serving Size 25 g Servings Per Container 4 --- The product is packaged in a clear plastic bottle.
Why the product was recalled
The product contained undeclared sulfites (735 ppm) based on sampling and analysis by New York State Department of Agriculture & Markets.
Distribution information
Nationwide (according to press release)
How to read the classification
FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Press Release.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.
FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.