Linkbio Corp. recalls LinkBio CORE Workstation
- Recalling company
- Linkbio Corp.
- 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.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Mar 12, 2026
- Reported
- Apr 22, 2026
- Distribution
- US Nationwide distribution in the state of Alabama, Florida, and Kansas.
- Status
- Ongoing
- Quantity
- 5 units
- Lot / codes
- Product Code: 87-9136. UDI-DI: 00810022403099. All serial numbers of the CORE Workstation are affected.
- Company location
- Rockaway, NJ
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-1810-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-1810-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.