Class II

Medical Device Recall: LinkBio CORE Workstation, a component of the CORE Shoulder System. Product Code: 87-9136.

Linkbio Corp. · March 12, 2026

Reason for Recall

The CORE Workstation may display an incorrect "Planning Date " when viewing cases on the "Start Case" menu screen.

Distribution

US Nationwide distribution in the state of Alabama, Florida, and Kansas.

States Affected

NATIONWIDE

Quantity Affected

5 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1810-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.