FDA Device recall Z-1113-2015
Athrosurface 40mm 13.75x31mm 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 Athrosurface 40mm 13.75x31mm 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-1113-2015 |
| 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
Athrosurface 40mm 13.75x31mm Taper Post Fixation Component; Catalog Number: 8135-1875 Part Number: 3135-1875. 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: 8135-1875 Part Number: 3135-1875 |
|---|
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-1113-2015%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.