# FDA recall Z-3018-2026

> **ConMed Corporation** · Class II · device recall initiated 2026-07-14.

## Product

CONMED Linvatec GENESYS CrossFT Suture Anchor with Disposable  Driver  REF# CFBC-5502B  5.5mm GENESYs CrossFT Suture Anchor with  two, #2 (5 metric) Hi-Fi Sutures  Sterile

## Reason for recall

Suture anchor may contain incorrect patient implant card which may result in incorrect device identification and traceability.

## Distribution

US Nationwide distribution in the state of TX.

## Key facts

- **Recall number:** Z-3018-2026
- **Recalling firm:** ConMed Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-07-14
- **Report date:** 2026-09-02

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Utica, NY, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-3018-2026

## Citation

> MORVS. FDA recall Z-3018-2026. Retrieved 2026-10-21 from https://api.morvs.ai/recall/Z-3018-2026. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*