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Kingston Pharma LLC Recall: Gas developing in sealed bottle.

United States

TerminatedClass II

Company
Kingston Pharma LLC
Product
Live Better Drug Free Black Elderberry Syrup, 4 FL OZ (118 m…
Recall date
January 29, 2018
Terminated
July 11, 2019
Source
FDA

Reason for recall

Gas developing in sealed bottle.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Live Better Drug Free Black Elderberry Syrup, 4 FL OZ (118 mL); DIETARY SUPPLEMENT, UPC 050428581186 050428581186 13,536 bottles KK170067; KK170070; K170071

Distribution

  • CVS Distribution Centers in the following states: Alabama
  • Florida
  • Indian
  • Michigan
  • New Jersey
  • New York
  • Pennsylvania
  • Rhode Island
  • South Carolina
  • Tennessee
  • Texas
  • Virginia.

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0796-2018
Event ID
79084
Status
Terminated
Classification
Class II
Company
Kingston Pharma LLC
Product description
Live Better Drug Free Black Elderberry Syrup, 4 FL OZ (118 mL); DIETARY SUPPLEMENT, UPC 050428581186
Quantity
13,536 bottles
Reason
Gas developing in sealed bottle.
Recall initiation date
January 29, 2018
Report date
February 21, 2018
Classification date
Not published in this source record
Termination date
July 11, 2019
Distribution pattern
CVS Distribution Centers in the following states: Alabama, Florida, Indian, Michigan, New Jersey, New York, Pennsylvania, Rhode Island, South Carolina, Tennessee, Texas, Virginia.
UPC, lot, and code information
UPC 050428581186; KK170067; KK170070; K170071
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: Kingston Pharma LLC

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Distribution
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Product
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Published
March 13, 2019
Distribution
USA: OH, FL, AZ, WI, MI, AL, CO, UT, NY,…

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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.