Hibiscus Lavender Syrup
Reason Hibiscus Lavender Syrup is recalled because the internal fill temperature noted on production records was below 165¿F.
Lemon Ginger Syrup recall
Recalled by Improper Goods · Portland, OR, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Lemon Ginger Syrup is recalled because the internal fill temperature of this product is not recorded.
These are failures of the safety steps that keep food safe - cooking, pasteurising, keeping cold, sealing - even when no contaminant has yet been found. All processing & sanitation problems recalls.
What was recalled
Lemon Ginger Syrup, packaged in 100 mL or 250 mL glass bottle. 100 mL bottle has UPC 8 53142 00504 0. 250 mL bottle has no UPC code. These bottles are also sold in the following cocktail kits: -Portland Pony -Dark and Stormy -Whiskey Ginger Smash -Sun Hat -Hibiscus Margarita The label is read in parts: "***RAFT LEMON GINGER***BOTANICAL COCKTAIL + SODA SYRUP***Slow-brewed in Portland, Oregon***Ingredients: Organic Cane Sugar, Water, Organic Ginger, Organic Orange Peel***Improper Goods, LLC 16313 NE Cameron Blvd. Portland, OR 97230***".
Quantity: 373/100 mL bottles and 51/250 mL bottles
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.
000417 USE BY 062009
Where it was sold
California Minnesota Missouri North Carolina New York Ohio Oregon Virginia Washington
FDA's distribution note: were distributed in CA, MN, MO, NC, NY, OH, OR, WA, and VA.
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. 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
- Improper Goods
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Feb 1, 2018
- In FDA report of
- Feb 21, 2018
- Terminated
- Apr 6, 2018
- FDA recall number
- F-0810-2018 · event 79109
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.