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Z-2217-2017 Class II Terminated

Recalled by Cardinal Scale Mfg Co — Webb City, MO

FDA device recall Z-2217-2017 was initiated by Cardinal Scale Mfg Co on December 23, 2015 and is designated Class II. Reason for recall: One complaint of a seat on a scale failing unexpectedly which can cause an injury. The recall status is terminated (terminated June 28, 2017). Affected quantity: 975 scales.

Recall Details

Product Type: Devices
Report Date: June 7, 2017
Initiation Date: December 23, 2015
Termination Date: June 28, 2017
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 975 scales

Product Description

Cardinal, Digital Bariatric Scale 1) model 6876, Cap 600 and 2) model 6868 Cap 1000

Reason for Recall

One complaint of a seat on a scale failing unexpectedly which can cause an injury.

Distribution Pattern

Worldwide distribution - US Nationwide in the states: Alabama, California, Colorado, Connecticut, Florida, Georgia, Illinois, Kansas, Kentucky, Maryland, Massachusetts, Michigan, Minnesota, Missouri, Nebraska, Nevada, NEW JERSEY, New York, NORTH CAROLINA, Ohio, Oregon, Pennsylvania, Rhode Island, South Dakota, Texas, Vermont, Virginia, Washington, West Virginia, Wisconsin, and Wyoming. Product was also distributed to the following foreign countries: Canada, Hong Kong, Kuwait, Pakistan,

Code Information

None.