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Ability Dynamics LLC recalls RUSH81 Prosthetic Foot Product Usage: Prosthetic foot for human use
Recalled June 25, 2014 · FDA recall Z-1825-2014 · Ability Dynamics
Hazard
Ability Dynamics is recalling RUSH81 Prosthetic Foot because the existing bolts may be bottomed out in the threaded hole and this could lead to bolt failure. · FDA Class II
Units
175 units
Sold at
Worldwide Distribution - US (nationwide) and in the countries of Australia and Canada.
Description
Ability Dynamics is recalling RUSH81 Prosthetic Foot because the existing bolts may be bottomed out in the threaded hole and this could lead to bolt failure.
Product
RUSH81 Prosthetic Foot Product Usage: Prosthetic foot for human use
Manufacturer(s)
Ability Dynamics LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →