Laerdal Medical AS, Stavanger Manufacturing
4 recall(s) on record — most severe on record: Class II.
Activity by year
- Recalls (4)
Devices registered here (1)
- Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)Product code MWI (opens in a new tab) · Class II · Cardiovascular · 21 CFR 870.2300
Recalls & enforcement
- Class IIOngoing2026-01-13units 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.
- Class IITerminated2020-12-18Component failures may cause the unit to lose all suction. Users will need to obtain alternate suction devices or methods, leading to a delay in treatment and, in worst case scenario, potential suffocation if alternative suction or ventilation method is not administered by the us…
- Class IITerminated2017-08-31A shipment of LCSU 4 suction units and canisters attempted importation into the United States but was refused by FDA for lack of necessary approvals with CDRH by the foreign firms.
- Class IITerminated2017-01-08The On/Off functionality in the LCSU 4 is controlled by electronic components, one of which might be damaged.
Related
- All facilities operated by LAERDAL MEDICAL A/S
- LAERDAL MEDICAL A/S (NO)
- LAERDAL MEDICAL (SUZHOU) CO., LTD. (CN)
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Laerdal Medical AS, Stavanger Manufacturing (FEI 3031563234) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3031563234-laerdal-medical-as-stavanger-manufacturi/
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