Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1341-2026 — 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;

U.S. FDA — Device Enforcement · United States · 2026-01-13 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1341-2026
Date of alert: 2026-01-13
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Laerdal Medical Corporation
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 07045432088519

Reported risk: 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.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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Recall Z-1341-2026 — 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;

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