RegWardenFDA facility compliance records
Recall

Class II — Cardinal Scale Mfg Co

Recalling firmCARDINAL SCALE MFG. CO.
Registered facilityCARDINAL SCALE MFG. CO. (the firm's only registered facility)
ClassificationClass II
StatusTerminated
ReasonOne complaint of a seat on a scale failing unexpectedly which can cause an injury.
ProductCardinal, Digital Bariatric Scale 1) model 6876, Cap 600 and 2) model 6868 Cap 1000
Quantity975 scales
DistributionWorldwide 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 wa…
Initiated2015-12-23
Classified2017-06-01
Terminated2017-06-28
Recall numberZ-2217-2017
InitiationVoluntary: Firm initiated

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Class II recall — Cardinal Scale Mfg Co (Z-2217-2017).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/76975/

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