RUSH81 Prosthetic Foot Product Usage: Prosthetic foot for human use — Class II medical device recall Z-1825-2014
Terminated recall by Ability Dynamics LLC, reported 2014-06-25, distributed nationwide. Ability Dynamics is recalling RUSH81 Prosthetic Foot because the existing bolts may be bottomed out in the thr
| Recall number | Z-1825-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Ability Dynamics LLC, Tempe, AZ, United States |
| Recall initiated | 2014-06-02 |
| Classified | 2014-06-18 |
| Reported by FDA | 2014-06-25 |
| Terminated | 2014-09-22 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CA |
| Quantity | 175 units |
| Serial numbers | B1300004, B1300005, B1300009, B1300010, B1300014, B1300015, B1300016, B1300020, B1300023, B1300025, B1300026, B1300029, B1300030, B1300032, B1300035, B1300036, B1300038, B1300043, B1300047, B1300048, B1300050, B1300051, B1300053, B1300056, B1300060 and 160 more |
Product
RUSH81 Prosthetic Foot Product Usage: Prosthetic foot for human use
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1825-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.