LinkBio CORE Workstation, a component of the CORE Shoulder… recallZ-1810-2026 · Linkbio Corp. · initiated Mar 12, 2026
Open, Classified
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from Linkbio Corp. or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
Why it was recalled
The CORE Workstation may display an incorrect "Planning Date " when viewing cases on the "Start Case" menu screen.
FDA root cause category: Under Investigation by firm
What the company is doing
LinkBio notified consignees on about 03/12/2026 via email. Consignees were instructed to take note of the potential inaccuracy of the "Planning Date," that no product was required to be returned, and to complete and return the Distributor Reply form. LinkBio Corp. is investigating the root cause of the time/date sync issue and will take appropriate action to ensure accurate dates are displayed for the user.
Recall details
- Recall number
- Z-1810-2026
- Status
- Open, Classified
- Initiated by the company
- Mar 12, 2026
- Posted by the FDA
- Apr 10, 2026
- Recalling firm
- Linkbio Corp.
- Quantity
- 5 units
- Product code
- QHE
- FDA submissions
- K241470
- Distribution
- US Nationwide distribution in the state of Alabama, Florida, and Kansas.
Product description
LinkBio CORE Workstation, a component of the CORE Shoulder System. Product Code: 87-9136.
Code information (models, lots, serial numbers)
Product Code: 87-9136. UDI-DI: 00810022403099. All serial numbers of the CORE Workstation are affected.
Devices named in this recall
1 device in the FDA device registry whose identifier appears in the recall's code information.
- CORE Shoulder System 87-9136Link Bio Corp · Shoulder Arthroplasty Implantation System1 recall1 report
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 16, 2026. Text above is shown as published by the FDA.
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