Linkbio Corp. recalls LinkBio CORE Workstation

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

LinkBio notified consignees on about 03/12/2026 via email. Consignees were instructed to take note of the potential inaccuracy of the "Planning Date," that no product was required to be returned, and to complete and return the Distributor Reply form. LinkBio Corp. is investigating the root cause of the time/date sync issue and will take appropriate action to ensure accurate dates are displayed for the user.

• FDA enforcement recordOfficial FDA database entry for Z-1810-2026
• FDA 510(k) clearance · K241470The device's official FDA premarket clearance record
• FDA device classification · QHEOfficial FDA classification for this device type
• CFR regulation · 21 CFR 888.3660The federal regulation governing this device
• FDA recall announcementSearch FDA.gov for the official press announcement
• Find Linkbio Corp.Search for the manufacturer's official notice
• News coverageRecent reporting on this recall and manufacturer
• openFDA data recordThe raw JSON record this page is built from

Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.