Linkbio Corp.: Shoulder Arthroplasty Implantation System
- Recalling firm
- 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
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-03-12
- Status
- Open, Classified
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- US Nationwide distribution in the state of Alabama, Florida, and Kansas.
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/9a129733-2417-4461-aabd-238daed74b12