FDA Device recall Z-1111-2015
Arthrosurface 25&30mm 12.5x32mm Taper Post Fixation Component
- FDA Device
- Class II
- terminated
- Published 2015-02-18
On 2015-02-18 the FDA classified a Class II recall of Arthrosurface 25&30mm 12.5x32mm Taper Post Fixation Component by Arthrosurface, citing fully threaded Taper Post Fixation components not cleared for marketing in the US with current indications.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1111-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-11-24 |
| Published | 2015-02-18 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Arthrosurface |
| Distribution | US |
Product
Arthrosurface 25&30mm 12.5x32mm Taper Post Fixation Component; Catalog Number: 6125-0035, Part Number: 1125-0035. HemiCAP Contoured Articular Prosthetic for Humeral head resurfacing. Orthopedic shoulder prosthesis component.
Reason
Fully threaded Taper Post Fixation components not cleared for marketing in the US with current indications.
Identifiers
| code_info | Catalog Number: 6125-0035, Part Number: 1125-0035 |
|---|
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-1111-2015%22
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