Tasty Peach Slices
Reason The dried fruit product contained undeclared sulfites (225.0 ppm) based on sampling and analysis by New York State Department of Agriculture and Markets.
Grassplot Ginger Slice recall
Recalled by Lion Pavilion Ltd. · Maspeth, NY, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
The product contained undeclared sulfites (735 ppm) based on sampling and analysis by New York State Department of Agriculture & Markets.
A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.
What was recalled
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.
Quantity: UNKNOWN
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
UPC 7246 6247 and no other coding
Where it was sold
Nationwide.
FDA's distribution note: Nationwide (according to press release)
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Lion Pavilion Ltd.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Feb 22, 2013
- In FDA report of
- Jul 22, 2015
- Terminated
- Jul 14, 2015
- FDA recall number
- F-2847-2015 · event 64466
- Official record
- FDA enforcement report search