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Improper Goods Recall: Lemon Ginger Syrup is recalled because the internal fill temperature of this product is not recorded.

United States

TerminatedClass II

Company
Improper Goods
Product
Lemon Ginger Syrup, packaged in 100 mL or 250 mL glass bottl…
Recall date
February 1, 2018
Terminated
April 6, 2018
Source
FDA

Reason for recall

Lemon Ginger Syrup is recalled because the internal fill temperature of this product is not recorded.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
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***". Not published in this source record 373/100 mL bottles and 51/250 mL bottles 000417 USE BY 062009

Distribution

  • were distributed in CA
  • MN
  • MO
  • NC
  • NY
  • OH
  • OR
  • WA
  • and VA.

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0810-2018
Event ID
79109
Status
Terminated
Classification
Class II
Company
Improper Goods
Product description
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
Reason
Lemon Ginger Syrup is recalled because the internal fill temperature of this product is not recorded.
Recall initiation date
February 1, 2018
Report date
February 21, 2018
Classification date
Not published in this source record
Termination date
April 6, 2018
Distribution pattern
were distributed in CA, MN, MO, NC, NY, OH, OR, WA, and VA.
UPC, lot, and code information
000417 USE BY 062009
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Other products recalled under this same event

This recall shares FDA event ID 79109 with 1 other product entry in Public Health Trace.

FDA Recall United States Terminated Historical recordClass II

Improper Goods

Product
Hibiscus Lavender Syrup, packaged in 100 mL or 250 mL glass…
Published
February 21, 2018
Distribution
were distributed in CA, MN, MO, NC, NY,…

View recall →

Responsible company: Improper Goods

Other recalls from Improper Goods

FDA Recall United States Terminated Historical recordClass II

Improper Goods

Product
Hibiscus Lavender Syrup, packaged in 100 mL or 250 mL glass…
Published
February 21, 2018
Distribution
were distributed in CA, MN, MO, NC, NY,…

View recall →

Distribution map

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.

Distribution map
State Distributed
California 1
Minnesota 1
Missouri 1
North Carolina 1
New York 1
Ohio 1
Oregon 1
Washington 1
Virginia 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.