FDA-Device2014-06-25Class II
RUSH81 Prosthetic Foot Product Usage: Prosthetic foot for human use
Ability Dynamics LLC
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.
Sold states
Worldwide Distribution - US (nationwide) and in the countries of Australia and Canada.
Affected count
175 units
Manufactured in
2082 E University Dr, N/A, Tempe, AZ, United States
Products
RUSH81 Prosthetic Foot Product Usage: Prosthetic foot for human use
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1825-2014Don't want to check this manually?
We email you a Sunday digest of new federal recalls relevant to parents — free, no credit card. Or upgrade to as-it-happens alerts for the brands you actually own.
Get the Sunday Brief