LinkBio CORE Workstation recall (Linkbio Corp.)
Medical deviceClass IIOngoing
Summary: Linkbio Corp. is recalling 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.
What is being recalled
LinkBio CORE Workstation, a component of the CORE Shoulder System. Product Code: 87-9136.
Why
The CORE Workstation may display an incorrect "Planning Date " when viewing cases on the "Start Case" menu screen.
How serious is it
Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
Where it was sold
US Nationwide distribution in the state of Alabama, Florida, and Kansas. (states named: Alabama, Florida, Kansas)
How to tell if yours is affected
Product Code: 87-9136. UDI-DI: 00810022403099. All serial numbers of the CORE Workstation are affected.
What to do
Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.
Recall facts
| Recall number | Z-1810-2026 |
| Category | Medical device |
| Agency | U.S. Food and Drug Administration (FDA) |
| Severity | Class II |
| Status | Ongoing |
| Recall started | March 12, 2026 |
| Reported | April 22, 2026 |
| Company | Linkbio Corp. |
| Company location | Rockaway, NJ, United States |
| Initiated by | Voluntary: Firm initiated |
| Quantity | 5 units |
More recalls from Linkbio Corp. · all medical device recalls · recalls from March 2026