Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
RUSH81 Prosthetic Foot Product Usage: Prosthetic foot for human use Recalled by Ability Dynamics LLC Due to Ability Dynamics is recalling RUSH81 Prosthetic Foot because...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Ability Dynamics LLC directly.
Affected Products
RUSH81 Prosthetic Foot Product Usage: Prosthetic foot for human use
Quantity: 175 units
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Ability Dynamics LLC
Ability Dynamics LLC has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report