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Reese Pharmaceutical Company Recall: The finished product label on the Cranberry supplement does not include Calcium. Users of the product may be unaware of the Calcium in the supplement. Additionally the amount per serving as written on the product label is incorrect and should be 500mg, not 900mg.

United States

TerminatedClass III

Company
Reese Pharmaceutical Company
Product
Good Neighbor Pharmacy Cranberry Tablets, Cranberry Suppleme…
Recall date
August 2, 2016
Terminated
August 2, 2017
Source
FDA

Reason for recall

The finished product label on the Cranberry supplement does not include Calcium. Users of the product may be unaware of the Calcium in the supplement. Additionally the amount per serving as written on the product label is incorrect and should be 500mg, not 900mg.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Good Neighbor Pharmacy Cranberry Tablets, Cranberry Supplement 450mg. Urinary Health. Tablets are packed in a labeled carton, 50 tablets per carton. Distributed by Amerisource Bergen 1300 Morris Drive Chesterbrook, PA 19087. Not published in this source record Not published in this source record Not published in this source record

Distribution

  • AL
  • AZ
  • CA
  • FL
  • GA
  • HI
  • IL
  • KY
  • MA
  • MI
  • MN
  • MO
  • NC
  • OH
  • PA
  • TX
  • UT
  • VA
  • WA

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-2194-2016
Status
Terminated
Classification
Class III
Company
Reese Pharmaceutical Company
Product description
Good Neighbor Pharmacy Cranberry Tablets, Cranberry Supplement 450mg. Urinary Health. Tablets are packed in a labeled carton, 50 tablets per carton. Distributed by Amerisource Bergen 1300 Morris Drive Chesterbrook, PA 19087.
Quantity
Not published in this source record
Reason
The finished product label on the Cranberry supplement does not include Calcium. Users of the product may be unaware of the Calcium in the supplement. Additionally the amount per serving as written on the product label is incorrect and should be 500mg, not 900mg.
Recall initiation date
August 2, 2016
Report date
September 21, 2016
Classification date
Not published in this source record
Termination date
August 2, 2017
Distribution pattern
AL, AZ, CA, FL, GA, HI, IL, KY, MA, MI, MN, MO, NC, OH, PA, TX, UT, VA, WA
UPC, lot, and code information
Not published in this source record
Voluntary or mandated
Not published in this source record
Initial notification method
Not published in this source record
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Reese Pharmaceutical Company

Other recalls from Reese Pharmaceutical Company

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Product
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Published
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Distribution
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FDA Recall United States TerminatedTerminated: June 4, 2018Historical recordClass II

Reese Pharmaceutical Company

Product
Berry Flavor Immune Support Dietary Supplement Effervescent…
Published
December 6, 2017
Distribution
Product was shipped to the following sta…

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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
Alabama 1
Arizona 1
California 1
Florida 1
Georgia 1
Hawaii 1
Illinois 1
Kentucky 1
Massachusetts 1
Michigan 1
Minnesota 1
Missouri 1
North Carolina 1
Ohio 1
Pennsylvania 1
Texas 1
Utah 1
Virginia 1
Washington 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.

This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.

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 III mean?

A situation in which use of or exposure to a product is not likely to cause adverse health consequences.

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.

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