FDA Device recall Z-1810-2026
LinkBio CORE Workstation, a component of the CORE Shoulder System
- FDA Device
- Class II
- ongoing
- Published 2026-04-22
On 2026-04-22 the FDA classified a Class II recall of LinkBio CORE Workstation, a component of the CORE Shoulder System by Linkbio, citing the CORE Workstation may display an incorrect "Planning Date " when viewing cases on the "Start Case" menu screen.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1810-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-03-12 |
| Published | 2026-04-22 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Linkbio |
| Distribution | US |
Product
LinkBio CORE Workstation, a component of the CORE Shoulder System. Product Code: 87-9136.
Reason
The CORE Workstation may display an incorrect "Planning Date " when viewing cases on the "Start Case" menu screen.
Identifiers
| code_info | Product Code: 87-9136. UDI-DI: 00810022403099. All serial numbers of the CORE Workstation are affected. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1810-2026%22
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