LinkBio CORE Workstation may display an incorrect planning date
LinkBio is recalling the CORE Workstation, a component of the CORE Shoulder System, because it may display an incorrect planning date on the Start Case menu screen.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: FDA Class II recall over an incorrect date shown on a menu screen, with no effect on the plan itself described, which fits the minor display and labeling band at Moderate.
Plain-English summary
LinkBio is recalling the CORE Workstation, product code 87-9136, UDI-DI 00810022403099, a component of the CORE Shoulder System. The action covers five units, and all serial numbers of the CORE Workstation are affected.
The CORE Workstation may display an incorrect Planning Date when viewing cases on the Start Case menu screen. The FDA classified the action as Class II. The source does not describe any effect on the surgical plan itself.
Distribution was within the United States, in Alabama, Florida and Kansas. The workstation is supplied to healthcare facilities rather than sold to consumers.
Facilities should identify affected units using the product code and UDI-DI above and follow the instructions issued by LinkBio.
The recalled product
- Product
- LinkBio CORE Workstation, a component of the CORE Shoulder System. Product Code: 87-9136.
- Manufacturer
- Linkbio Corp.
- Affected units
- 5
Distribution
Related recalls
Same manufacturer · Linkbio Corp.
See all →- HighLINK SymphoKnee System Femoral Augment Recalled for Incorrect Implant in Packaging
FDA (Devices) · 2023-06-07
- ModerateLINK SLED Knee Implant Surgical Technique Update Required
FDA (Devices) · 2023-05-10
- HighLINK SLED Knee Implant Component Recalled Due to Early Loosening Risk
FDA (Devices) · 2023-05-10
- HighKnee implant system recall due to aseptic loosening from improper surgical technique
FDA (Devices) · 2023-05-10
- HighKnee Implant Recall Due to Risk of Aseptic Loosening and Wear
FDA (Devices) · 2023-05-10
Same hazard · display error
See all →- ModerateKico Knee Innovation Recalls ARVIS Surgical Navigation System Due to Sensor Issue
FDA (Devices) · 2026-08-26
- ModerateSpectral Instruments Recalls 35 Ami HTX X-Ray Units
FDA (Devices) · 2026-08-26
- ModerateSpectral Instruments Lago X Medical Device Recalled for Display Glitch
FDA (Devices) · 2026-08-26
- HighHexagon Purus Recalls Tern RC8 Vehicles Due to Brake Display Error
NHTSA · 2026-04-20
- HighMedical Imaging Software Recall: mint Lesion Orientation Display Malfunction
FDA (Devices) · 2024-12-25