# FDA recall Z-1810-2026

> **Linkbio Corp.** · Class II · device recall initiated 2026-03-12.

## Product

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

## Reason for recall

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

## Distribution

US Nationwide distribution  in the state of Alabama, Florida, and Kansas.

## Key facts

- **Recall number:** Z-1810-2026
- **Recalling firm:** Linkbio Corp.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-03-12
- **Report date:** 2026-04-22

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Rockaway, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1810-2026

## Citation

> AI Analytics. FDA recall Z-1810-2026. Retrieved 2026-07-27 from https://api.ai-analytics.org/recall/Z-1810-2026. Source: US FDA. Licensed CC0.

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