Home/Recalls/FDA-Z-1810-2026
FDA DevicesClass II

LinkBio CORE Workstation, a component of the CORE Shoulder System. Product Code: 87-9136.

Published: April 22, 2026Recall ID: Z-1810-2026Category: devicesCountry: US
US
Medical DeviceFDA DevicesUSUS

LinkBio CORE Workstation, a component of the CORE Shoulder System. Product Code: 87-9136.

Recalling Firm: Linkbio Corp.

Reason for Recall / Hazard

The CORE Workstation may display an incorrect "Planning Date " when viewing cases on the "Start Case" menu screen.

Product Description & Identification

LinkBio CORE Workstation, a component of the CORE Shoulder System. Product Code: 87-9136.

Additional Source Details

FieldValue
CityRockaway
StateNJ
Event id98594
Address 1101 Round Hill Dr Ste 7
Address 2N/A
Code infoProduct Code: 87-9136. UDI-DI: 00810022403099. All serial numbers of the CORE Workstation are affected.
Postal code07866-1214
Report date20260422
Product typeDevices
Product quantity5 units
Reason for recallThe CORE Workstation may display an incorrect "Planning Date " when viewing cases on the "Start Case" menu screen.
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20260312
Initial firm notificationE-Mail
Center classification date20260410

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Overview

  • Recalling FirmLinkbio Corp.
  • StatusOngoing
  • Risk LevelClass II
  • DistributionUS Nationwide distribution in the state of Alabama, Florida, and Kansas.
Recall Hazard Severity
High Alert (Class I)
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🚨 SAFETY ALERT: Linkbio Corp. - LinkBio CORE Workstation, a component of the CORE Shoulder System. Product Code: 87-9136.

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https://therecallfile.com/recalls/linkbio-core-workstation-a-component-of-the-core-shoulder-system-produ/FDA-Z-1810-2026
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