Drug recall
RUSH81 Prosthetic Foot Product Usage: Prosthetic foot for human use
FDA recall event 68535 · Class II · Ability Dynamics LLC
Key facts
| Event ID | 68535 |
|---|---|
| Recall numbers | Z-1825-2014 |
| Recalling firm | Ability Dynamics LLC |
| Product type | Devices |
| Products | RUSH81 Prosthetic Foot Product Usage: Prosthetic foot for human use |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | 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. |
| Initiation date | Jun 2, 2014 |
| Report date | Jun 25, 2014 |
| Termination date | Sep 22, 2014 |
| City | Tempe |
| State | AZ |
| Country | United States |
| FEI number | 3008584163 |
At a glance
- 1–9 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: