# FDA recall Z-1741-2025

> **AVID Medical, Inc.** · Class II · device recall initiated 2025-03-31.

## Product

Halyard CHRIST SUTURE KIT. General Procedure Tray Convenience Kit

## Reason for recall

An issue with a raw material used to coat some surgical needles that may result in diminished performance and/or removal of some silicone needle coating during use.

## Distribution

US Nationwide distribution in the states of IL & LA.

## Key facts

- **Recall number:** Z-1741-2025
- **Recalling firm:** AVID Medical, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-03-31
- **Report date:** 2025-05-21

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Toano, VA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1741-2025

## Citation

> AI Analytics. FDA recall Z-1741-2025. Retrieved 2026-07-15 from https://api.ai-analytics.org/recall/Z-1741-2025. Source: US FDA. Licensed CC0.

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