Z-1810-2026 Class II Ongoing
FDA device recall Z-1810-2026 was initiated by Linkbio Corp. on March 12, 2026 and is designated Class II. Reason for recall: The CORE Workstation may display an incorrect "Planning Date " when viewing cases on the "Start Case" menu screen. The recall status is ongoing. Affected quantity: 5 units.
Recall Details
- Product Type
- Devices
- Report Date
- April 22, 2026
- Initiation Date
- March 12, 2026
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 5 units
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.
Distribution Pattern
US Nationwide distribution in the state of Alabama, Florida, and Kansas.
Code Information
Product Code: 87-9136. UDI-DI: 00810022403099. All serial numbers of the CORE Workstation are affected.