# FDA recall Z-1341-2026

> **Laerdal Medical Corporation** · Class II · device recall initiated 2026-01-13.

## Product

Laerdal Compact Suction Unit 4   RTCA version (LCSU 4   RTCA)  1) LCSU 4, 800 ml, RTCA; Catalog Number: 880052;  2) LCSU 4, 300 ml, RTCA; Catalog Number: 880062;  3) LCSU 4, RTCA; Catalog Number: 881152;

## Reason for recall

units manufactured in a limited time period may emit electromagnetic noise beyond the acceptable limits for RTCA application specified in RTCA DO-160G Chapter 21, Equipment Category M.

## Distribution

Worldwide distribution - US Nationwide and the countries of Denmark, Sweden, Norway, Canada, Finland, Australia, Spain, France, United Kingdom, Italy, Korea, Germany, Netherlands, Switzerland, New Zealand, Singapore, Malaysia, Austria.

## Key facts

- **Recall number:** Z-1341-2026
- **Recalling firm:** Laerdal Medical Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-01-13
- **Report date:** 2026-02-18

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1341-2026

## Citation

> AI Analytics. FDA recall Z-1341-2026. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-1341-2026. Source: US FDA. Licensed CC0.

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