# FDA recall Z-2268-2024

> **Stryker Sustainability Solutions** · Class II · device recall initiated 2024-05-10.

## Product

Stryker Sustainability Solutions, BW Lasso 2515 NAV eco Variable Diagnostic EP Catheter, REF: D134301, ELECTRODES: 22,  spacing:2-6-2MM, Length 115 cm, STERILE.EO, Rx Only

## Reason for recall

Diagnostic electrophysiology (EP) catheters do not meet testing requirements.

## Distribution

International distribution to the country of Japan.

## Key facts

- **Recall number:** Z-2268-2024
- **Recalling firm:** Stryker Sustainability Solutions
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-05-10
- **Report date:** 2024-07-10

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2268-2024

## Citation

> AI Analytics. FDA recall Z-2268-2024. Retrieved 2026-06-30 from https://api.ai-analytics.org/recall/Z-2268-2024. Source: US FDA. Licensed CC0.

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