RegWardenFDA facility compliance records
Facility

Laerdal Medical AS, Stavanger Manufacturing

4 recall(s) on record — most severe on record: Class II.

Activity by year

FDA actions on record by year2017: 2 recalls; 2020: 1 recalls; 2026: 1 recalls2201720182019120202021202220232024202512026
  • 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 IIOngoing2026-01-13
    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.
  • Class IITerminated2020-12-18
    Component 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 IITerminated2017-08-31
    A 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 IITerminated2017-01-08
    The On/Off functionality in the LCSU 4 is controlled by electronic components, one of which might be damaged.

Related

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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