# FDA recall Z-1674-2023

> **Linkbio Corp.** · Class II · device recall initiated 2023-04-25.

## Product

LINK SymphoKnee System L-Shaped Femoral Augment, Medial-Right/Lateral-Left, Sz 5-6  Tilastan, cemented.  Intended for primary and revision total knee replacement.  Item Number: 880-325/13

## Reason for recall

Contains the incorrect implant in the packaging. The packaging incorrectly contains the opposite side of the implant (Lateral-Right/Medial-Left instead of Medial-Right/Lateral-Left).

## Distribution

US Nationwide Distribution - AL, GA, IL, IN, LA, NV, TX

## Key facts

- **Recall number:** Z-1674-2023
- **Recalling firm:** Linkbio Corp.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-04-25
- **Report date:** 2023-06-07

- **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-1674-2023

## Citation

> AI Analytics. FDA recall Z-1674-2023. Retrieved 2026-06-12 from https://api.ai-analytics.org/recall/Z-1674-2023. Source: US FDA. Licensed CC0.

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