Laerdal Compact Suction Unit (LCSU) 4

Official notice

19 Nov 2020

Last checked

19 Nov 2020

High riskACCC

An official ACCC notice concerns Laerdal Compact Suction Unit (LCSU) 4. Delay in suctioning secretions, blood or vomit blocking the airways can lead to suffocation if an alternative suction or ventilation method is not administered by the user. Published 2020-11-19.

What to do now

Laerdal will contact affected consumers in writing to arrange for replacement of the affected product. Upon receiving the replacement, consumers should dispose of the pump unit, but keep the carry bag, battery, external power supply and wire stand of the existing unit. Prior to receiving the replacement pump, consumers may continue to use the LCSU4 by following the recommendations below: 1. Do not block the patient tube for more than 10 seconds at a time at vacuum levels greater than 300mmHg; 2. Only use the approved accessories; and 3. Once the desired vacuum level is reached unblock the patient tube immediately. For further information, please contact Laerdal Customer Service by phone on 1800 331 565 (Monday to Friday, 8.30am - 5pm AEST)

Recall number

c501de07-5476-4877-9f6f-5d56def42d64

Official notice

2020-11-19

The hazard

Delay in suctioning secretions, blood or vomit blocking the airways can lead to suffocation if an alternative suction or ventilation method is not administered by the user.

How to check if you're affected

Compare the product name and identifiers below with the item you own. Follow the official notice if they match.

Artg Numbers

205931

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Affected products

Product 1

Laerdal Compact Suction Unit 4 Catalogue numbers: 880051, 880061, 881151, 880052, 880062 and 881152 Manufacturing Dates (format YYYYMMDD) in the range 20180809 to 20200606 Serial Numbers in the range 1808090001 to 2006060045 ARTG 205931 (Laerdal Pty Ltd - Manual emergency suction system) The LCSU 4 is a portable, electrically powered, medical suction device intended for field and transport use. It is intended for intermittent operation to remove secretions, blood or vomit from a patient’s airway to allow ventilation.

Risk / hazard

Delay in suctioning secretions, blood or vomit blocking the airways can lead to suffocation if an alternative suction or ventilation method is not administered by the user.

Where it was sold

The source does not list specific retailers. See the official notice for where affected products were sold.

Location 1

AU · Australia

Affected area 1

AU · Australia

Source & status

Source

Tier

beta

Category

HOME

Classification

Pharmacy and medical products

App estimate

high

Recall details

Recall number

c501de07-5476-4877-9f6f-5d56def42d64

Classification

Pharmacy and medical products

Source tier

beta

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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