
Laerdal · Model V-VAC Manual Suction Unit
Catridge capacity: 425 ml canister. Does not contain latex.
Compiled for this model from its own documentation and established engineering knowledge for this equipment class - not from a verified service record. Confirm against the manufacturer's service manual.
Symptoms: Weak or no vacuum at the patient port, slow to pull down, will not reach rated vacuum.
Root cause: Worn pump diaphragm / vanes, an air leak in the lid / tubing / overflow float, or a blocked filter.
Symptoms: Suction drops suddenly, fluid near the pump, filter wet.
Root cause: Overflow shut-off triggered or a saturated / clogged bacteria filter.
Symptoms: Pump noisy, hot, runs slow, or trips its thermal cut-out.
Root cause: Worn motor bearings or pump head.
Symptoms: Short run time, will not power on off mains.
Root cause: Aged battery.
Symptoms: Gauge inaccurate or vacuum will not regulate.
Root cause: Gauge or regulator wear.
Serviceable items for this model, compiled from its documentation and engineering knowledge for this equipment class. Service class and relative cost are estimates, not manufacturer figures; no part numbers are given. Confirm intervals and pricing against the manufacturer.
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Pump diaphragm / vane kit | Periodic replacement | $$ | Moderate |
| Hydrophobic / bacteria filter | Consumable | $ | Easy |
| Collection-jar lid seals & float | Frequent wear item | $ | Easy |
| Motor / pump head | Major service part | $$$ | Difficult |
| Battery (portable) | Periodic replacement | $$ | Fairly easy |
Relative cost: $ lowest · $$$$ highest service-part cost for this equipment class. Not a price.
Preventive-maintenance tasks typical of this equipment class. Perform to the manufacturer's procedure and your facility's policy - this is general reference, not a schedule for this specific unit.
A starting sequence for this model, compiled from its documentation and engineering knowledge for this equipment class. Follow the manufacturer's service documentation for the actual procedure.
Where this class of equipment is typically deployed - general reference, not this unit's own placement record.
Synced live from the FDA openFDA API.
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.
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 user.
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.
The On/Off functionality in the LCSU 4 is controlled by electronic components, one of which might be damaged.
Describe a symptom or error code. Bio answers from this device's own documented error codes, failure modes, parts, and guides.
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