- Recalling firm
- Linkbio Corp.
- Reason for recall
- The CORE Workstation may display an incorrect "Planning Date " when viewing cases on the "Start Case" menu screen.
- Affected products (lot / model / serial)
- Product Code: 87-9136. UDI-DI: 00810022403099. All serial numbers of the CORE Workstation are affected.
- Units affected
- 5 units
- Distribution pattern
- US Nationwide distribution in the state of Alabama, Florida, and Kansas.
- Firm location
- Rockaway, NJ, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- E-Mail
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-1810-2026
- Recall initiated
- March 12, 2026
- FDA classification date
- April 10, 2026
- FDA report date
- April 22, 2026
- FDA event ID
- 98594
- Last updated on HTM Vibe
- July 24, 2026