FDA Device recall Z-1825-2014
RUSH81 Prosthetic Foot Product Usage: Prosthetic foot for human use
- FDA Device
- Class II
- terminated
- Published 2014-06-25
On 2014-06-25 the FDA classified a Class II recall of RUSH81 Prosthetic Foot Product Usage: Prosthetic foot for human use by Ability Dynamics, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1825-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-06-02 |
| Published | 2014-06-25 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Ability Dynamics |
| Distribution | US |
Product
RUSH81 Prosthetic Foot Product Usage: Prosthetic foot for human use
Reason
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.
Identifiers
| code_info | Serial Numbers: B1400045 B1400085 B1400272 B1400352 B1400101 B1400344 B1300083 B1400133 B1400114 B1300030 B1…Serial Numbers: B1400045 B1400085 B1400272 B1400352 B1400101 B1400344 B1300083 B1400133 B1400114 B1300030 B1400290 B1400297 B1400197 B1400305 B1300043 B1400264 B1300080 B1400024 B1400087 B1300073 B1400108 B1400330 B1400138 B1300056 B1400261 B1400210 B1400321 B1400337 B1400300 B1400323 B1400351 B1400103 B1400104 B1400156 B1400173 B1400202 B1400222 B1400232 B1400253 B1400269 B1300062 B1400296 B1400258 B1400083 B1400111 B1300084 B1400135 B1400294 B1400031 B1400036 B1400162 B1300082 B1400102 B1400050 B1400051 B1400076 B1400084 B1300038 B1300025 B1400288 B1400280 B1400281 B1400312 B1400018 B1400252 B1400245 B1400260 B1400128 B1400201 B1400215 B1400308 B1400071 B1400033 B1400058 B1400213 B1400196 B1400214 B1400203 B1400204 B1400115 B1400212 B1400144 B1400319 B1400238 B1300072 B1300074 B1400336 B1400335 B1300061 B1400174 B1400175 B1400171 B1400194 B1300050 B1400059 B1400025 B1300036 B1400074 B14 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1825-2014%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.