Linkbio Corp.
What this record is not
A recall record is reproduced as FDA published it, and the classification is FDA’s. SPEQ adds no interpretation, and a recall concerns the products and dates in the record — it is not a statement about a company’s other products or its current status.
The CORE Workstation may display an incorrect "Planning Date " when viewing cases on the "Start Case" menu screen.
LinkBio CORE Workstation, a component of the CORE Shoulder System. Product Code: 87-9136.
Product Code: 87-9136. UDI-DI: 00810022403099. All serial numbers of the CORE Workstation are affected.
Data: U.S. FDA. 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. Open the enforcement explorer →