FDA Device recall Z-1495-2017
Orthosize Templating Version 1.2.6 Echo Bi-Metric Hip Stem Digital Templates
- FDA Device
- Class II
- terminated
- Published 2017-03-29
On 2017-03-29 the FDA classified a Class II recall of Orthosize Templating Version 1.2.6 Echo Bi-Metric Hip Stem Digital Templates by Zimmer Biomet, citing digital templates were created with the incorrect files.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1495-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-02-14 |
| Published | 2017-03-29 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Zimmer Biomet |
| Distribution | US |
Product
Orthosize Templating Version 1.2.6 Echo Bi-Metric Hip Stem Digital Templates. For preoperative planning of orthopedic surgery.
Reason
Digital templates were created with the incorrect files.
Identifiers
| code_info | Orthosize Templating Version 1.2.6 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1495-2017%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.