FDA Medical devices recall ·
LinkBio CORE Workstation, a component of the CORE Shoulder System recall
- Recall number
- Z-1810-2026
- Date
- (initiated March 12, 2026)
- Company / brand
- Linkbio Corp.
101 Round Hill Dr Ste 7, Rockaway, NJ, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 5 units
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
LinkBio CORE Workstation, a component of the CORE Shoulder System. Product Code: 87-9136.
Why was it recalled?
The CORE Workstation may display an incorrect "Planning Date " when viewing cases on the "Start Case" menu screen.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Product Code: 87-9136. UDI-DI: 00810022403099. All serial numbers of the CORE Workstation are affected.
Distribution
US Nationwide distribution in the state of Alabama, Florida, and Kansas.
States: Alabama Florida Kansas
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-1810-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.