← FDA ENFORCEMENT
Z-1810-2026Class II

Linkbio Corp.

Recalling firm
Linkbio Corp.
Product type
Device
Status
Ongoing
Report date
2026-04-22
Distribution
US Nationwide distribution in the state of Alabama, Florida, and Kansas.
Firm state
NJ
Product quantity
5 units
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Documentation & Change Control
Reason for recall

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

Product description

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

Code / lot info

Product Code: 87-9136. UDI-DI: 00810022403099. All serial numbers of the CORE Workstation are affected.

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Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.