FDA DevicesClass II
LinkBio CORE Workstation, a component of the CORE Shoulder System. Product Code:...
Published: April 22, 2026Recall ID: Z-1810-2026Category: devicesCountry: US
Reason for Recall / Hazard
The CORE Workstation may display an incorrect "Planning Date " when viewing cases on the "Start Case" menu screen.
Product Description & Identification
LinkBio CORE Workstation, a component of the CORE Shoulder System. Product Code: 87-9136.
Additional Source Details
| Field | Value |
|---|---|
| City | Rockaway |
| State | NJ |
| Event id | 98594 |
| Address 1 | 101 Round Hill Dr Ste 7 |
| Address 2 | N/A |
| Code info | Product Code: 87-9136. UDI-DI: 00810022403099. All serial numbers of the CORE Workstation are affected. |
| Postal code | 07866-1214 |
| Report date | 20260422 |
| Product type | Devices |
| Product quantity | 5 units |
| Reason for recall | The CORE Workstation may display an incorrect "Planning Date " when viewing cases on the "Start Case" menu screen. |
| Voluntary mandated | Voluntary: Firm initiated |
| Recall initiation date | 20260312 |
| Initial firm notification | |
| Center classification date | 20260410 |
Overview
- Recalling FirmLinkbio Corp.
- StatusOngoing
- Risk LevelClass II
- DistributionUS Nationwide distribution in the state of Alabama, Florida, and Kansas.