FDA recall record

Ability Dynamics RUSH81 Prosthetic Foot Product Usage: Prosthetic foot for human use recall — FDA Z-1825-2014

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…

Class IIclassification
Z-1825-2014official record ID
Jun 25, 2014report date

Recall record at a glance

Official recordZ-1825-2014
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmAbility Dynamics LLC
Report dateJun 25, 2014
Recall initiation dateJun 2, 2014
Quantity175 units
LocationTempe, AZ, United States

Official product description

RUSH81 Prosthetic Foot Product Usage: Prosthetic foot for human use

Why the product was 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.

Distribution information

Worldwide Distribution - US (nationwide) and in the countries of Australia and Canada.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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