# FDA recall Z-2194-2026

> **Stryker Sustainability Solutions** · Class II · device recall initiated 2026-04-10.

## Product

Daig Livewire Steerable, Product Number 401914; REPROCESSED ELECTROPHYSIOLOGY CATHETER

## Reason for recall

Incomplete seals on sterile product

## Distribution

US Nationwide and the countries of Israel and Canada.

## Key facts

- **Recall number:** Z-2194-2026
- **Recalling firm:** Stryker Sustainability Solutions
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-04-10
- **Report date:** 2026-05-20

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Tempe, AZ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2194-2026

## Citation

> MORVS. FDA recall Z-2194-2026. Retrieved 2026-10-13 from https://api.morvs.ai/recall/Z-2194-2026. Source: US FDA. Licensed CC0.

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