Laerdal Compact Suction Unit 4 RTCA version — Class II medical device recall Z-1341-2026
Ongoing recall by Laerdal Medical Corporation, reported 2026-02-18, distributed nationwide. units manufactured in a limited time period may emit electromagnetic noise beyond the acceptable limits for RT
| Recall number | Z-1341-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Laerdal Medical Corporation, Wappingers Falls, NY, United States |
| Recall initiated | 2026-01-13 |
| Classified | 2026-02-11 |
| Reported by FDA | 2026-02-18 |
| Distributed | Nationwide (US) |
| Countries outside the US | AT, AU, CA, CH, DE, DK, ES, FI, FR, GB, IT, KR, MY, NL, NO, NZ, SE, SG |
| UPC / GTIN / UDI-DI | 07045432067132, 07045432088519, 07045432088533 |
| Model numbers | 880052, 880062, 881152 |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1341-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.