Recall Z-1810-2026— Linkbio Corp.

Name: FDA recall Z-1810-2026
Creator: U.S. Food and Drug Administration
Published: 2026-03-12

Class II · Ongoing

Class II FDA medical device recall by Linkbio Corp., initiated 2026-03-12. It names one FDA 510(k) clearance: K241470. 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..

Recalling firm: Linkbio Corp.
Classification: Class II
Status: Ongoing
Initiated: 2026-03-12
Firm location: Rockaway, NJ, United States

510(k) clearances named in this recall

1 on FDA's record

K241470 — CORE Shoulder SystemLinkBio Corp.·cleared 2025-02-20

K-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.

Product description

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

Reason for recall

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

Data sourced from openFDA. This site is unofficial and independent of the FDA.