Medical device recalls Moderate risk

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

Recall date
March 12, 2026
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1810-2026
FDA classification
Class II
Brand / firm
Linkbio Corp.
Sold / distributed
US Nationwide distribution in the state of Alabama, Florida, and Kansas.

Why it was recalled

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

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

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

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