LAERDAL MEDICAL A/S
4 recall(s) on record — most severe on record: Class II.
Recalls by year
- Recalls (4)
Registered facilities (3)
- LAERDAL MEDICAL A/S FEI 3002807435 · NO
- LAERDAL MEDICAL (SUZHOU) CO., LTD. FEI 3004993040 · CN
- Laerdal Medical AS, Stavanger Manufacturing FEI 3031563234 · NO
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.
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. We restate the public record only — measured facts, never risk verdicts.
Cite this record
RegWarden. “LAERDAL MEDICAL A/S — FDA compliance profile.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/company/oo-9038993-laerdal-medical-a-s/
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