# FDA recall Z-2445-2024

> **LINK BIO CORP** · Class II · device recall initiated 2024-06-27.

## Product

LINK SymphoKnee Patella Sizing Template, Item Number 881-509/00

## Reason for recall

The LinkSymphoKnee Patella Sizing Template was incorrectly labeled. The markings on two arms of the instrument were mixed up because the triangular Patella Sizing Template was inserted upside down into the laser marking process.

## Distribution

US Nationwide distribution in the states of FL, GA, KS, OH, WI.

## Key facts

- **Recall number:** Z-2445-2024
- **Recalling firm:** LINK BIO CORP
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-06-27
- **Report date:** 2024-07-31

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2445-2024

## Citation

> AI Analytics. FDA recall Z-2445-2024. Retrieved 2026-07-04 from https://api.ai-analytics.org/recall/Z-2445-2024. Source: US FDA. Licensed CC0.

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